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Heavy periods and Female sexual symptoms and Heel itch and Indecision in adults
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Results: Causes of Heavy periods AND Female sexual symptoms AND Heel itch AND Indecision in adults

    1. Chronic Kidney Disease
     Long-term and generally irreversible disease of the kidneys due to infection, obstruction, congenital diseases or generalised diseases causing failure of the kidneys' normal functions....read more »

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Note: Do not use for diagnosis; see limitations of results.

Results: 546 causes of Heavy periods OR Female sexual symptoms OR Heel itch OR Indecision in adults

    1. 18p minus syndrome
     A rare chromosomal disorder where a portion of chromosome 18 is missing which is characterized by mental and growth deficiencies, drooping upper eyelid and prominent ears. The type and severity of symptoms is determined by the amount of genetic material t...more »
    2. 3-Beta-HSD, Deficiency of
     A rare condition where the deficiency of a particular enzyme (3-Beta-Hydroxysteroid Dehydrogenase) results in reduced levels of adrenal hormones - mineralocorticoids, glucocorticoids and sex steroids. The condition results in variable degrees of salt wast...more »
    3. 3-Beta-Hydroxysteroid Dehydrogenase deficiency
     A rare condition where the deficiency of a particular enzyme (3-Beta-Hydroxysteroid Dehydrogenase) results in reduced levels of adrenal hormones - mineralocorticoids, glucocorticoids and sex steroids. The condition results in variable degrees of salt wast...more »
    4. 3-Beta-Hydroxysteroid Dehydrogenase, Type II, Deficiency of
     A rare condition where the deficiency of a particular enzyme (3-Beta-Hydroxysteroid Dehydrogenase) results in reduced levels of adrenal hormones - mineralocorticoids, glucocorticoids and sex steroids. The condition results in variable degrees of salt wast...more »
    5. 3?-hydroxysteroid dehydrogenase deficiency
     A ver rare form of congenital adrenal hyperplasia involving a deficiency of 3?-hydroxysteroid dehydrogenase which results in reduced production of adrenal steroids (mineralocorticoids, sex steroids and glucocorticoids). The disorder can occur in classical...more »
    6. 46,XX chromosome 7 deletion p13-p21
     A chromosomal disorder where a small portion of chromosome 7 is deleted which results in a range of abnormalities....more »
    7. 46,XX testicular DSD
     A sex chromosome disorder in males which affects gonadal development and causes infertility. Males have XX chromosomes instead of the normal XY....more »
    8. 46,XX testicular disorder of sex development
     A sex chromosome disorder in males which affects gonadal development and causes infertility. Males have XX chromosomes instead of the normal XY....more »
    9. 47,XXX syndrome
     A genetic condition where females have an extra X chromosome in each of their cells. Normally female cells have two X chromosomes. This is not usually an inherited condition but a defect that occurs during cell division. Often the condition is asymptomati...more »
    10. AIDS-Related Opportunistic Infections
     A term given to HIV patients who have a low CD4 count (below 200) which means that they have low levels of a type of immune cell called T-cells. AIDS patients tend to develop opportunistic infections and cancers. Opportunistic infections are infections th...more »
    11. Abdominal Cancer
     Growth of abnormal cells (tumour) affecting the organs in the abdominal cavity; may be due to primary growth of a tumour or spread from another tumour (metastases, secondary tumour)...more »
    12. Abruptio Placentae
     Placental bleeding usually late in a pregnancy....more »
    13. Achard-Thiers Syndrome
     A hormonal disorder that occurs in diabetic postmenopausal women. It is characterized by diabetes mellitus and hirsuitism....more »
    14. Acquired prothrombin deficiency
     A deficiency of prothrombin (vital for blood clotting) which is acquired through other conditions such as liver disease, anticoagulant drugs or vitamin K deficiency. The severity of symptoms is determined by the degree of deficiency....more »
    15. Acromegaloid, Cutis Verticis Gyrata, Corneal Leukoma Syndrome
     A rare condition characterized by the association of acromegaly, cutis verticis gyrate and corneal leukoma....more »
    16. Actinomycetales infection
     A bacterial infection from the order of Actinobacteria. The range of symptoms is variable depending on which bacteria from the order is involved....more »
    17. Acute (or transient) urinary incontinence
     Acute (or Transient) Incontinence is caused by a new or recent medical problem that can be treated....more »
    18. Acute leukaemia of ambiguous lineage
     A term used to describe a type of leukemia (a blood cancer) where the leukemic cells cannot be determined as myeloid or lymphoid or where both types of cells are present....more »
    19. Acute myeloblastic leukemia type 1
     A form of blood cancer resulting in the rapid proliferation of immature blood cells (blast cells)....more »
    20. Acute myeloblastic leukemia type 2
     A form of blood cancer resulting in the rapid proliferation of granulocytes and monocytes....more »
    21. Acute myeloblastic leukemia type 3
     A rare form of malignant bone marrow cancer involving the rapid proliferation of immature precursors of blood cells. Type 3 involves the proliferation of promyelocytes....more »
    22. Acute myeloblastic leukemia type 6
     A rare form of malignant bone marrow cancer involving the rapid proliferation of immature precursors of blood cells. Type 6 involves the proliferation of the immature precursors of red blood cells called erythroblasts....more »
    23. Acute myelocytic leukemia
     A cancer of the blood-forming tissues of the bone marrow involving the proliferation of cells that normally develop into infection-fighting cells such as eosinophils, monocytes, basophils and neutrophils. The cancerous cells replace the normal bone marrow...more »
    24. Acute myeloid leukaemia and myelodysplastic syndromes related to alkylating agent
     The use of alkylating agents to treat cancer can result in leukemia in some patients....more »
    25. Acute myeloid leukaemia and myelodysplastic syndromes related to topoisomerase type II inhibitor
     The use of topoisomerase type II inhibitors to treat cancer can result in leukemia in some patients....more »
    26. Acute myeloid leukaemia and myelodysplastic syndromes, therapy related
     Certain cancer therapies can result in the development of leukemia in some patients. These therapies includes topoisomerase type II inhibitors and alkylating agents....more »
    27. Acute myeloid leukemia
     A form of rapidly progressing blood cancer resulting in the rapid proliferation of granulocytes and monocytes, red blood cells and platelets....more »
    28. Acute myeloid leukemia, adult
     A form of blood cancer resulting in the rapid proliferation of granulocytes and monocytes, red blood cells and platelets....more »
    29. Acute non lymphoblastic leukemia
     A form of rapidly progressing blood cancer resulting in the rapid proliferation of granulocytes and monocytes, red blood cells and platelets. It is one of the most common forms of leukemia in adults but can occur in children....more »
    30. Addison's Disease
     A rare progressive hormonal disorder characterized by insufficient production of certain hormones called adrenal corticosteroids....more »
    31. Adenocarcinoma, Clear Cell
     A type of cancer that occurs mainly in the genitourinary tract and the cells that make up the tumor are clear. It is very rare and most cases occur in females whose mothers used a drug called DES (synthetic estrogen) while pregnant....more »
    32. Adenomyosis
     A rare disorder where the endometrium (lining of the uterus) grows inside the muscle walls of the uterus. The condition is generally harmless but can be very painful....more »
    33. Adnexal and Skin Appendage Neoplasms
     A type of tumour that develops on particular organs - eyes, skin and uterus. The tumors are usually benign but some may become malignant. The symptoms will vary depending on the location of the tumor and whether it is benign or malignant. These type of tu...more »
    34. Adrenal Cancer
     A malignant cancer that develops in the adrenal gland. The tumor may be nonfunctioning (does not produce hormones) or functioning in which case excessive levels of hormones can cause a variety of symptoms depending on which hormone is involved. Adrenal ho...more »
    35. Adrenal Cortex Diseases
     Diseases of the adrenal cortex. Examples includes Addison's disease, Cushing's syndrome and adrenal fatigue....more »
    36. Adrenal Cortex Neoplasms
     A tumor that develops in the adrenal gland. The tumor may be nonfunctioning (does not produce hormones) or functioning in which case excessive levels of hormones can cause a variety of symptoms depending on which hormone is involved. Adrenal hormones made...more »
    37. Adrenal Hyperplasia, Congenital (General)
     Congenital adrenal hyperplasia is an inherited condition characterized by adrenal insufficiency. It is caused by a deficiency in an enzyme needed to produce certain adrenal hormones such as cortisol and aldosterone....more »
    38. Adrenal adenoma, familial
     A benign tumor that develops in the adrenal gland and tends to run in families. The tumor may be nonfunctioning (does not produce hormones) or functioning in which case excessive levels of hormones can cause a variety of symptoms depending on which hormon...more »
    39. Adrenal gland hyperfunction
     Excessive activity of the adrenal gland which causes excessive production of one or more adrenal hormones (aldosterone, corticosteroids, androgenic steroids, epinephrine and norepinephrine). The increased adrenal gland activity may be caused by an adrenal...more »
    40. Adrenal hyperplasia, congenital type 3
     A group of disorders that occur when a deficiency of 21-hydroxylase impairs the normal process of making adrenal corticosteroids. The severity of the condition is variable depending on the degree of deficiency....more »
    41. Adrenal hyperplasia, congenital, due to 11-Beta-hydroxylase deficiency
     A rare form of congenital adrenal hyperplasia characterized by a deficiency of 11-Beta-hydroxylase which results in excess androgen production and hypertension. The disorder can occur in virilizing, hypertensive and salt-wasting forms and symptoms may ran...more »
    42. Adrenal hypoplasia congenital, X-linked
     A genetic disorder which affects the body tissues that produce hormones. It is characterized by underdeveloped adrenal glands which results adrenal insufficiency and hypogonadotrophic hypogonadism....more »
    43. Adrenal incidentaloma
     A tumor of the adrenal gland that is discovered incidentally while performing an imaging examination for reasons other than an adrenal tumor. The tumor may be asymptomatic or can causes excessive secretion of adrenal hormones and resulting symptoms. The t...more »
    44. Adrenocortical carcinoma
     A condition which is characterized by malignancy which affects the adrenocortex....more »
    45. Adrenoleukodystrophy
     A rare disorder which has characteristic symptoms of Addison disease (adrenocortical insufficiency) and Schilder disease (cerebral sclerosis). Bronze skin, brain sclerosis and demyelination are the main symptoms....more »
    46. Aging
     The medical conditions from getting older....more »
    47. Ahumada-Del Castillo Syndrome
     A rare endocrine disorder characterized by dysfunction of the pituitary and hypothalamus glands in women....more »
    48. Alcoholism
     Alcoholism is the compulsive urge to drink alcohol despite knowing the negative impact on one's health....more »
    49. Allen-Masters syndrome
     Damage to muscle layers in the pelvis which allows the abnormally increased movement of the cervix. It often occurs after a traumatic surgical birth, induced abortion or excessive vaginal packing....more »
    50. Allergic seminal vulvovaginitis
     Vaginal inflammation following contact with semen after ejaculation....more »
    51. Alport syndrome with leukocyte inclusions and macrothrombocytopenia
     A rare condition characterized by the presence of large blood platelets, kidney inflammation, deafness and abnormal leukocytes. End-stage kidney disease occurs in about a third of patients and tends to occur during the 3rd and 4th decades of life....more »
    52. Amenorrhea
     Absence of menstrual periods due to many possible causes....more »
    53. Amphetamine abuse
     Use of the stimulant drugs known as amphetamines or "speed"...more »
    54. Androgen Insensitivity Syndrome
     Females with male XY genetics but inability to respond to testosterone....more »
    55. Androgen insensitivity syndrome, partial
     A rare inherited condition where males are partially insensitive to the male hormones which results in varying degrees of feminization. The effect of the condition can range from the presence of normal female sexual characteristics to normal male sexual c...more »
    56. Anemia
     Reduced ability of blood to carry oxygen from various possible causes....more »
    57. Anemia, Iron-Deficiency
     A lack of fully functioning red blood cells due to a deficiency of iron. The iron allows the body to make hemoglobin in red blood cells which in turn allows the red blood cell to carry oxygen....more »
    58. Anemia, Refractory, with Excess of Blasts
     A bone marrow disease which results in insufficient red blood cells in the blood (anemia). The prognosis is poor with death usually occurring within a couple of years. There are two types: type 1 refers to cases where the level of blasts is less than 10% ...more »
    59. Anemia, Refractory, with Excess of Blasts, type 1
     A bone marrow disease which results in insufficient red blood cells in the blood (anemia). The prognosis is poor with death usually occurring within a couple of years. Type 1 refers to cases where the level of blasts is less than 10% and type 2 refers to ...more »
    60. Anemia, Refractory, with Excess of Blasts, type 2
     A bone marrow disease which results in insufficient red blood cells in the blood (anemia). The prognosis is poor with death usually occurring within a couple of years. Type 1 refers to cases where the level of blasts is less than 10% and type 2 refers to ...more »
    61. Anorexia
     Any type of appetite loss; often refers to anorexia nervosa...more »
    62. Anorexia Nervosa
     A disorder where a distorted sense of body image leads to self-starvation to the point of death in some cases....more »
    63. Anorexia nervosa, genetic types
     There is mounting evidence that anorexia nervosa may be caused by genetic factors which when combined with psychosocial factors can increase a persons risk of developing the condition....more »
    64. Anovulation
     Failure to ovulate...more »
    65. Anti-Social Personality Disorder
     A psychiatric condition characterized by chronic behavioral and social problems which often involves criminal behaviour....more »
    66. Asherman's syndrome
     Scarring and adhesions that develop in the uterus and can result in menstrual and fertility problems....more »
    67. Atherosclerosis
     Atherosclerosis is a syndrome affecting arterial blood vessels. It is a chronic inflammatory response in the walls of arteries, in large part due to the accumulation of macrophage white blood cells and promoted by low density (especially small particle) l...more »
    68. Atrophic vaginitis
     Type of vaginitis usually related to aging and menopause...more »
    69. Attention Deficit Hyperactivity Disorder
     Behavioral disorder with hyperactivity and/or inattention....more »
    70. Attenuated congenital adrenal hyperplasia
     A late onset form of congenital adrenal hyperplasia where insufficient adrenal corticosteroids are produced by the body due to the deficiency of a particular chemical. The severity of symptoms varies from person to person and onset may occur as early as c...more »
    71. Autoimmune Endometriosis
     An endometriosis that is caused by an autoimmune reaction...more »
    72. Autoimmune Hepatitis
     Liver inflammation caused due to autoimmune processes where the body's immune system attacks the liver....more »
    73. Autoimmune Thrombocytopenia
     Autoimmune disorder causing a lack of blood platelets....more »
    74. Autoimmune oophoritis
     An autoimmune condition where the body's own immune system attacks the ovaries and causes them to become inflamed. It can lead to ovarian function stopping prematurely....more »
    75. Autoimmune thyroid disease associated Celiac Disease
     Patients with autoimmune thyroid disease are more susceptible to developing celiac disease than the average population. Celiac disease is an autoimmune disorder characterized by intolerance to gluten by the small intestine. The type and severity of sympto...more »
    76. Autoimmune thyroid diseases
     Autoimmune diseases of the thyroid gland....more »
    77. Autonomic neuropathy
     A disorder of the nervous system concerned with regulation of activity of cardiac muscle, smooth muscle, and glands, usually restricted to the sympathetic and parasympathetic systems...more »
    78. Bacterial toxic-shock syndrome
     A very rare, potentially fatal infection caused by toxins produced by bacteria, especially bacteria such as Staphylococcus aureus or Streptococcus pyogenes. The condition is often associated with tampon use but can originate from other sources....more »
    79. Balanitis xerotica obliterans
     Dermatological condition affecting male genetalia. Characterised by atrophic white patches and white indurarted tissue at the tip preventing retraction....more »
    80. Bamforth syndrome
     A rare syndrome characterized mainly by the association of an abnormal opening in the roof of the mouth and reduced thyroid functioning....more »
    81. Bardet-Biedl syndrome, type 1
     A rare genetic disorder characterized by mental retardation, obesity, polydactyly and retinal pigmentation as well as other abnormalities. Type 1 is caused by a defect in chromosome 11q13....more »
    82. Bardet-Biedl syndrome, type 10
     A rare genetic disorder characterized by mental retardation, obesity, polydactyly and retinal pigmentation as well as other abnormalities. Type 10 is caused by a defect in chromosome 12q....more »
    83. Bardet-Biedl syndrome, type 11
     A rare genetic disorder characterized by mental retardation, obesity, polydactyly and retinal pigmentation as well as other abnormalities. Type 11 is caused by a defect in chromosome 9q33.1....more »
    84. Bardet-Biedl syndrome, type 12
     A rare genetic disorder characterized by mental retardation, obesity, polydactyly and retinal pigmentation as well as other abnormalities. Type 12 is caused by a defect in chromosome 4q27....more »
    85. Bardet-Biedl syndrome, type 2
     A rare genetic disorder characterized by mental retardation, obesity, polydactyly and retinal pigmentation as well as other abnormalities. Type 2 is caused by a defect in chromosome 16q21....more »
    86. Bardet-Biedl syndrome, type 3
     A rare genetic disorder characterized by mental retardation, obesity, polydactyly and retinal pigmentation as well as other abnormalities. Type 3 is caused by a defect in chromosome 3p12-q13....more »
    87. Bardet-Biedl syndrome, type 4
     A rare genetic disorder characterized by mental retardation, obesity, polydactyly and retinal pigmentation as well as other abnormalities. Type 4 is caused by a defect in chromosome 15q22.3....more »
    88. Bardet-Biedl syndrome, type 5
     A rare genetic disorder characterized by mental retardation, obesity, polydactyly and retinal pigmentation as well as other abnormalities. Type 5 is caused by a defect in chromosome 2q31....more »
    89. Bardet-Biedl syndrome, type 6
     A rare genetic disorder characterized by mental retardation, obesity, polydactyly and retinal pigmentation as well as other abnormalities. Type 6 is caused by a defect in chromosome 20p12....more »
    90. Bardet-Biedl syndrome, type 7
     A rare genetic disorder characterized by mental retardation, obesity, polydactyly and retinal pigmentation as well as other abnormalities. Type 7 is caused by a defect in chromosome 4q27....more »
    91. Bardet-Biedl syndrome, type 8
     A rare genetic disorder characterized by mental retardation, obesity, polydactyly and retinal pigmentation as well as other abnormalities. Type 8 is caused by a defect in chromosome 14q32.11....more »
    92. Bardet-Biedl syndrome, type 9
     A rare genetic disorder characterized by mental retardation, obesity, polydactyly and retinal pigmentation as well as other abnormalities. Type 9 is caused by a defect in chromosome 7p14....more »
    93. Bartholin's abscess
     Abscess in a small vaginal gland...more »
    94. Bartholin's cyst
     Cyst in a small vaginal gland...more »
    95. Bearn-Kunkel syndrome
     A type of autoimmune liver disease characterized by liver damage, very high blood gammaglobulin levels and increased plasma cells....more »
    96. Bernard-Soulier Syndrome
     A rare inherited blood coagulation disorder caused by blood platelet abnormalities which results in easy bruising and excessive bleeding....more »
    97. Biemond syndrome type 2
     A rare inherited condition characterized by mental retardation, obesity, polydactyly and underdeveloped genitals....more »
    98. Birth control pill poisoning
     Birth control pill contain hormones such as estrogen and progestin and excessive ingestion of the pills can result in relatively minor symptoms - usually there are no serious problems associated with the ingested of many birth control pills at one time. T...more »
    99. Blepharophimosis, Ptosis, Epicanthus Inversus Syndrome
     A rare genetic disorder characterized by inner canthal folds, lateral displacement of inner canthi and drooping upper eyelid. The severity of symptoms is variable. There are two subtypes of the condition: Type 2 involves eye anomalies as well as female fe...more »
    100. Blepharophimosis, Ptosis, Epicanthus Inversus Syndrome, type 1
     A rare genetic disorder characterized by inner canthal folds, lateral displacement of inner canthi and drooping upper eyelid. The severity of symptoms is variable. There are two subtypes of the condition: Type 2 involves eye anomalies as well as female fe...more »
    101. Blepharophimosis, ptosis, epicanthus inversus
     A rare genetic disorder characterized by inner canthal folds, lateral displacement of inner canthi and drooping upper eyelid....more »
    102. Bone-Marrow failure syndromes
     A disorder where the bone marrow fails to produce enough new blood cells....more »
    103. Boucher-Neuhauser syndrome
     A very rare disorder characterized by spinocerebellar ataxia, eye abnormalities and a failure of the pituitary to stimulate gonadal development during puberty....more »
    104. Breisky disease
     A progressive wasting disease of the vulva that occurs in postmenopausal women and is probably caused by hormonal imbalance....more »
    105. Brenner tumor of the vagina
     A Brenner tumour usually occurs in the ovaries but can sometimes occur in the vagina. The tumor is generally benign....more »
    106. Bulimia nervosa
     Eating disorder with binging (overeating) and purging (vomiting)....more »
    107. CCFDN
     A rare, recessively inherited syndrome characterized by cataracts during infancy, unusual facial appearance and neuropathy....more »
    108. CIN
     A premalignant condition of the cervix that can progress into cervical cancer....more »
    109. Candidiasis
     Fungal infection of moist areas such as mouth or vagina...more »
    110. Cardiomyopathy, hypogonadism, collagenoma syndrome
     A rare inherited condition characterized primarily by skin nodules. The skin nodules may be associated with organ system involvement resulting in a variety of other symptoms....more »
    111. Celiac Disease
     Digestive intolerance to gluten in the diet....more »
    112. Celiac disease, susceptibility to 1
     The susceptibility to developing celiac disease due to a genetic defect on chromosome 6p21.3. Celiac disease is a small intestine disorder where the ingestion of foods containing wheat gluten and similar proteins leads to the inflammation of the small int...more »
    113. Celiac disease, susceptibility to 10
     The susceptibility to developing celiac disease due to a genetic defect on chromosome 3q25-q26. Celiac disease is a small intestine disorder where the ingestion of foods containing wheat gluten and similar proteins leads to the inflammation of the small i...more »
    114. Celiac disease, susceptibility to 11
     The susceptibility to developing celiac disease due to a genetic defect on chromosome 3q28. Celiac disease is a small intestine disorder where the ingestion of foods containing wheat gluten and similar proteins leads to the inflammation of the small intes...more »
    115. Celiac disease, susceptibility to 12
     The susceptibility to developing celiac disease due to a genetic defect on chromosome 6q25.3. Celiac disease is a small intestine disorder where the ingestion of foods containing wheat gluten and similar proteins leads to the inflammation of the small int...more »
    116. Celiac disease, susceptibility to 13
     The susceptibility to developing celiac disease due to a genetic defect in the SH2B3 gene on chromosome 12q24. Celiac disease is a small intestine disorder where the ingestion of foods containing wheat gluten and similar proteins leads to the inflammation...more »
    117. Celiac disease, susceptibility to 2
     The susceptibility to developing celiac disease due to a genetic defect on chromosome 5q31-q33. Celiac disease is a small intestine disorder where the ingestion of foods containing wheat gluten and similar proteins leads to the inflammation of the small i...more »
    118. Celiac disease, susceptibility to 3
     The susceptibility to developing celiac disease due to a genetic defect on chromosome 2q33. Celiac disease is a small intestine disorder where the ingestion of foods containing wheat gluten and similar proteins leads to the inflammation of the small intes...more »
    119. Celiac disease, susceptibility to 4
     The susceptibility to developing celiac disease due to a genetic defect on chromosome 19p13.1. Celiac disease is a small intestine disorder where the ingestion of foods containing wheat gluten and similar proteins leads to the inflammation of the small in...more »
    120. Celiac disease, susceptibility to 5
     The susceptibility to developing celiac disease due to a genetic defect on chromosome 15q11-q13. Celiac disease is a small intestine disorder where the ingestion of foods containing wheat gluten and similar proteins leads to the inflammation of the small ...more »
    121. Celiac disease, susceptibility to 6
     The susceptibility to developing celiac disease due to a genetic defect on chromosome 4q27. Celiac disease is a small intestine disorder where the ingestion of foods containing wheat gluten and similar proteins leads to the inflammation of the small intes...more »
    122. Celiac disease, susceptibility to 7
     The susceptibility to developing celiac disease due to a genetic defect on chromosome 1q31. Celiac disease is a small intestine disorder where the ingestion of foods containing wheat gluten and similar proteins leads to the inflammation of the small intes...more »
    123. Celiac disease, susceptibility to 8
     The susceptibility to developing celiac disease due to a genetic defect on chromosome 2q11-q12. Celiac disease is a small intestine disorder where the ingestion of foods containing wheat gluten and similar proteins leads to the inflammation of the small i...more »
    124. Celiac disease, susceptibility to 9
     The susceptibility to developing celiac disease due to a genetic defect on chromosome 3p21. Celiac disease is a small intestine disorder where the ingestion of foods containing wheat gluten and similar proteins leads to the inflammation of the small intes...more »
    125. Cephalothoracic progressive lipodystrophy
     A rare acquired disorder that involves adipose tissue abnormalities and is characterized by loss of adipose tissue mainly in the trunk and arms....more »
    126. Cervical Cancer
     Cervical cancer is malignant cancer of the cervix uteri or cervical area...more »
    127. Cervical polyps
     Benign polyps on the cervix of the uterus...more »
    128. Cervicitis
     Inflammation of the cervix...more »
    129. Cervix conditions
     Conditions of the cervix (entrance) of the female uterus....more »
    130. Chancroid
     An sexually transmitted disease caused by the Haemophilus ducreyi bacteria and is characterized by painful genital ulceration....more »
    131. Chapple syndrome
     A rare birth disorder characterized by painful menstruation, knees bent back and a uterus that is tilted backwards (retroverted). It is believed to be caused by an abnormal fetal position inside the womb....more »
    132. Chemical addiction
     Addiction to and abuse of various substances....more »
    133. Chiari-Frommel syndrome
     A rare condition where galactorrhea and amenorrhea continues for an abnormal length of time (generally longer than 6 months) after giving birth....more »
    134. Childbirth
     Delivery of a fetus by a pregnant woman....more »
    135. Chlamydia
     Common sexually transmitted disease often without symptoms....more »
    136. Cholera
     An acute bacterial disease transmitted through food or water contaminated with human faeces. The intestinal infection is caused by the bacterium Vibrio cholerae....more »
    137. Cholestasis disease of pregnancy
     A liver condition that can occur usually in the last stage of pregnancy. The flow of bile in the gallbladder or liver is impaired by the high levels of pregnancy hormones. The bile acids build up in the organs and then enter the bloodstream. The main symp...more »
    138. Choriocarcinoma
     Rare cancer of the placenta...more »
    139. Chromosome 15q duplication syndrome
     A rare chromosomal disorder involving an extra copy of genetic material from the long arm of chromosome 15. The type and severity of symptoms are determined by the amount and location of the duplicated genetic material....more »
    140. Chromosome 15q, trisomy
     A rare chromosomal disorder involving an extra copy of genetic material from the long arm of chromosome 15. The type and severity of symptoms are determined by the amount and location of the duplicated genetic material....more »
    141. Chromosome 17p, partial deletion
     A rare chromosomal disorder involving deletion of genetic material from the short arm of chromosome 17. The type and severity of symptoms are determined by the amount and location of the lost genetic material....more »
    142. Chromosome 18p minus syndrome
     A rare genetic disorder where a portion of the genetic material from the short arm of chromosome18 is missing. The symptoms or severity may vary somewhat between patients....more »
    143. Chromosome 18q, partial deletion
     A rare chromosomal disorder involving deletion of genetic material from the long arm of chromosome 18. The type and severity of symptoms are determined by the amount and location of the lost genetic material....more »
    144. Chromosome 6q duplication syndrome
     A rare chromosomal disorder involving duplication of the long arm (q) of chromosome 6 which results in various abnormalities depending on the size and location of the portion of duplicated genetic material....more »
    145. Chromosome 7, Partial Deletion of Short Arm
     A rare chromosomal disorder where part of the short arm (p) of chromosome 7 is deleted resulting in various abnormalities which are determined by the size and location of the deleted portion....more »
    146. Chromosome 7, partial monosomy 7p
     A rare chromosomal disorder where part of the short arm (p) of chromosome 7 is deleted resulting in various abnormalities which are determined by the size and location of the deleted portion....more »
    147. Chromosome 8 recombinant syndrome
     A rare recombinant chromosomal disorder involving chromosome 8 which results in various abnormalities....more »
    148. Chromosome 9 trisomy syndrome
     A rare chromosomal disorder where there are three copies of chromosome 9 in the body's cells instead of the normal two resulting in various abnormalities....more »
    149. Chromosome 9, Tetrasomy 9p
     A rare chromosomal disorder where there is four copies of the short arm of chromosome 9 instead of the normal two resulting in various abnormalities....more »
    150. Chromosome 9, trisomy
     A rare chromosomal disorder where there are three copies of chromosome 9 in the body's cells instead of the normal two resulting in various abnormalities. The type and severity of symptoms varies depending on the amount and exact location of the genetic m...more »
    151. Chromosome 9p tetrasomy syndrome
     A rare chromosomal disorder where there is four copies of the short arm of chromosome 9 instead of the normal two resulting in various abnormalities....more »
    152. Chronic Alcoholism -- Teratogenic Agent
     There is strong evidence to indicate that chronic alcoholism during pregnancy may have a teratogenic effect on the fetus. A teratogen is a substance that can cause birth defects. The likelihood and severity of defects may be affected by the level of expos...more »
    153. Chronic Kidney Disease
     Long-term and generally irreversible disease of the kidneys due to infection, obstruction, congenital diseases or generalised diseases causing failure of the kidneys' normal functions....more »
    154. Chronic interstitial cystitis
    155. Chronic renal insufficiency
     Chronic lack of function of the renal system. Kidneys....more »
    156. Chudley syndrome 1
     A rare syndrome characterized by mental retardation, obesity, hypogonadism and a distinctive mouth....more »
    157. Cirrhosis of the liver
     Scarring of the liver from alcohol or other causes....more »
    158. Clotting disorders
     Disorder with excessive clotting...more »
    159. Coagulopathy
     A disorder of the blood where it fails to clot normally....more »
    160. Collagenous celiac disease
     Collagenous celiac disease is used to describe progressive celiac disease characterized by the presence of a layer of collagen (scarring) in the intestinal layers. This form of celiac disease usually fails to respond to treatments such as gluten-free diet...more »
    161. Complete androgen insensitivity
    162. Condyloma
     A type of wart transmitted through direct sexual contact and is caused by the human papilloma virus....more »
    163. Congenital adrenal hyperplasia -- non-classical form
     A late onset form of congenital adrenal hyperplasia where insufficient adrenal corticosteroids are produced by the body due to the deficiency of a particular chemical. The severity of symptoms varies from person to person and onset may occur as early as c...more »
    164. Congenital adrenal hyperplasia -- simple virilizing form in females
     A group of disorder that occur when a deficiency of 21-hydroxylase impairs the normal process of making adrenal corticosteroids. The simple virilizing form involves a moderate deficiency of 21-hydroxylase and differs in its effects on males and females....more »
    165. Contact dermatitis
     Skin reaction to an irritant...more »
    166. Cortisone reductase deficiency
     An inborn error of steroid metabolism due to a deficiency of an enzyme called cortisone reductase (11-beta-hydroxysteroid dehydrogenase). This enzyme is needed to convert cortisone to cortisol....more »
    167. Cushing syndrome, familial
     A hormonal disorder caused by high levels of the cortisol hormone due to the abnormal development of the adrenal gland....more »
    168. Cushing's disease
    169. Cushing's syndrome
     A rare syndrome where excessive secretion of corticosteroids by the adrenal cortex leads to a variety of symptoms. Hormone-secreting adrenal or pituitary tumors are often the cause of the excessive corticosteroid secretion....more »
    170. Cystic Fibrosis
     Cystic fibrosis is a hereditary disease affecting the exocrine (mucus) glands of the lungs, liver, pancreas, and intestines, causing progressive disability due to multisystem failure....more »
    171. Cystocele
     Bladder falls down into the vagina....more »
    172. De la Chapelle syndrome
     A sex chromosome disorder in males which affects gonadal development and causes infertility. Males have XX chromosomes instead of the normal XY....more »
    173. Deafness -- cataracts -- skeletal anomalies
     A rare disorder characterized by deafness, cataracts and skeletal abnormalities as well as other anomalies....more »
    174. Deafness hypogonadism syndrome
     A rare condition characterized by the combination of hypogonadism and deafness....more »
    175. Depression
     Various syndromes with excessive anxiety, phobias, or fear....more »
    176. Dermoid cyst
     Benign cystic tumor often containing skin, hair, and other tissue...more »
    177. Diabetes Mellitus, Noninsulin-Dependent, Susceptibility to, 1
     Noninsulin-dependent diabetes (Type 2 diabetes) is a type of diabetes that doesn't respond to insulin but does tend to respond to dietary measures and diabetes medication. Researchers have discovered a number of genes which are linked to an increased risk...more »
    178. Diabetes Mellitus, Noninsulin-Dependent, Susceptibility to, 2
     Noninsulin-dependent diabetes (Type 2 diabetes) is a type of diabetes that doesn't respond to insulin but does tend to respond to dietary measures and diabetes medication. Researchers have discovered a number of genes which are linked to an increased risk...more »
    179. Diabetes Mellitus, Noninsulin-Dependent, Susceptibility to, 3
     Noninsulin-dependent diabetes (Type 2 diabetes) is a type of diabetes that doesn't respond to insulin but does tend to respond to dietary measures and diabetes medication. Researchers have discovered a number of genes which are linked to an increased risk...more »
    180. Diabetes Mellitus, Noninsulin-Dependent, Susceptibility to, 4
     Noninsulin-dependent diabetes (Type 2 diabetes) is a type of diabetes that doesn't respond to insulin but does tend to respond to dietary measures and diabetes medication. Researchers have discovered a number of genes which are linked to an increased risk...more »
    181. Diabetic neuropathy
     Nerve damage from diabetes affecting any body part; most commonly feet....more »
    182. Dicoumarol -- Teratogenic Agent
     There is evidence to indicate that exposure to Dicoumarol during pregnancy may have a teratogenic effect on the fetus. A teratogen is a substance that can cause birth defects. The likelihood and severity of defects may be affected by the level of exposure...more »
    183. Diethylstilbesterol -- Teratogenic Agent
     There is strong evidence to indicate that the use of Diethylstilbesterol during pregnancy may cause a teratogenic effect on the fetus. A teratogen is a substance that can cause birth defects. The likelihood and severity of defects may be affected by the l...more »
    184. Diphtheria
     Infectious bacterial respiratory disease...more »
    185. Double uterus-hemivagina-renal agenesis
     A very rare malformation of the uterus and vagina....more »
    186. Down's syndrome associated Celiac Disease
     Patients with Down's syndrome have a high degree of susceptibility to developing celiac disease. Up to 17% of Down's syndrome sufferers develop celiac disease but this rate varies amongst age groups and country of origin. Celiac disease is an autoimmune d...more »
    187. Drug abuse
     Addiction to any of various illicit drugs....more »
    188. Dysfunctional Uterine Bleeding
     Uterus bleeding unrelated to periods...more »
    189. Dysmenorrhea
     Pain, cramping, or discomfort due to menstruation...more »
    190. Dyspareunia
     Vaginal pain after sexual intercourse...more »
    191. Dystrophia myotonica 1
     A rare genetic disorder characterized by myotonia, muscle atrophy, cataracts and hypogonadism....more »
    192. Eating disorders
     Various mental disorders impairing normal eating or appetite....more »
    193. Ectopic pregnancy
     A condition where a fertilized egg embeds itself outside the uterus....more »
    194. Eczema
     Eczema is a chronic skin condition characterized by skin inflammation and irritation. The severity of extent of the condition is highly variable. It may be caused by allergies, irritants or other factors such as stress....more »
    195. Edwardsiella tarda infection
     A type of bacterial infection. The bacterium (Edwardsiella tarda) infects freshwater-dwelling animals and transmission occurs through consuming infected animals or contact with contaminated water. Symptoms are determined by the location of the infection. ...more »
    196. Ehlers-Danlos syndrome
     A group of inherited connective tissue disorders primarily involving the joints and skin. There are 11 disorders in the group....more »
    197. Endometrial Cancer
     Cancer of the endometrium (uterus lining)....more »
    198. Endometrial conditions
     Conditions that affect the female endometrium that is located in the uterus...more »
    199. Endometrial hyperplasia
     Thickening of the endometrium (lining of the uterus)...more »
    200. Endometrial stromal sarcoma
     A rare type of cancer that develops from the endometrial layer of the uterus. The cancer may be slow-growing or aggressive and may metastasize....more »
    201. Endometriosis
     Misplaced uterus tissue causing scar tissue....more »
    202. Endometritis
     Inflammation of the endometrium (uterine lining)...more »
    203. Epstein's Syndrome
     A syndrome characterized by the association of kidney disease, deafness and a blood disorder....more »
    204. Essential thrombocytosis -- same as essential thrombocythemia
     A rare blood disorder where the blood contains too many platelets due to excessive megakaryocytes (platelet-producing cells). Platelets are essential for blood clotting but in essential thrombocythemia excessive platelets can cause the blood to form abnor...more »
    205. Ewing's family of tumors
     A rare condition where tumors develop in bone or soft tissue. Usually teenagers are affected....more »
    206. Excessive dieting
     Excessive limitation of food intake can lead to problems and effects such as dizziness, depression, intestinal problems, edema and impaired growth....more »
    207. Factor V and factor VIII, combined deficiency of
     A rare inherited blood disorder where a deficiency of Factor V and factor VIII results in bleeding problems. Factor V and factor VIII is involved in blood coagulation....more »
    208. Factor V deficiency
     An inherited disorder where the deficiency of a blood component affects its ability to clot properly which can lead to bleeding problems. The severity of the disorder can vary from easy bruising to life-threatening hemorrhages....more »
    209. Factor VII deficiency
     A rare inherited blood disorder caused by a deficiency of a blood protein called Factor VII and resulting in poor blood coagulation. The severity of the condition is variable....more »
    210. Factor X deficiency
     A rare blood clotting disorder which may be inherited or acquired in people suffering from conditions such as liver disease, amyloidosis, leprosy and certain cancers. The underlying cause is the deficiency of a protein (Factor X) which is needed for the b...more »
    211. Factor X deficiency -- Friuli
     A rare inherited blood clotting disorder where there is a deficiency of a protein (Factor X) which is needed for the blood to clot properly. The Fruili variant tends to only cause moderate bleeding problems and occurs mainly in an area of Italy called Fru...more »
    212. Factor X deficiency -- Kanazawa
     A rare inherited blood clotting disorder where there is a deficiency of a protein (Factor X) which is needed for the blood to clot properly. The Kanazawa variant results in reduced Factor X blood clotting activity....more »
    213. Factor X deficiency -- Ketchikan
     A rare inherited blood clotting disorder where there is a deficiency of a protein (Factor X) which is needed for the blood to clot properly. The Ketchikan variant results in reduced Factor X blood clotting activity....more »
    214. Factor X deficiency -- Nottingham
     A rare inherited blood clotting disorder where there is a deficiency of a protein (Factor X) which is needed for the blood to clot properly. The Nottingham variant results in reduced Factor X blood clotting activity....more »
    215. Factor X deficiency -- Padua
     A rare inherited blood clotting disorder where there is a deficiency of a protein (Factor X) which is needed for the blood to clot properly. The Padau variant results in reduced Factor X blood clotting activity....more »
    216. Factor X deficiency -- San Antonio
     A rare inherited blood clotting disorder where there is a deficiency of a protein (Factor X) which is needed for the blood to clot properly. The San Antonia variant results in 14% of normal Factor X blood clotting activity....more »
    217. Factor X deficiency -- Santo Domingo
     A rare inherited blood clotting disorder where there is a deficiency of a protein (Factor X) which is needed for the blood to clot properly. The Santo Domingo variant results in reduced Factor X blood clotting activity....more »
    218. Factor X deficiency -- Shanghai
     A rare inherited blood clotting disorder where there is a deficiency of a protein (Factor X) which is needed for the blood to clot properly. The Shangai variant results in reduced Factor X blood clotting activity....more »
    219. Factor X deficiency -- St. Louis II
     A rare inherited blood clotting disorder where there is a deficiency of a protein (Factor X) which is needed for the blood to clot properly. The St. Louis II variant results in reduced Factor X blood clotting activity....more »
    220. Factor X deficiency -- Stockton
     A rare inherited blood clotting disorder where there is a deficiency of a protein (Factor X) which is needed for the blood to clot properly. The Stockton variant results in reduced Factor X blood clotting activity....more »
    221. Factor X deficiency -- Taunton
     A rare inherited blood clotting disorder where there is a deficiency of a protein (Factor X) which is needed for the blood to clot properly. The Taunton variant results in reduced Factor X blood clotting activity....more »
    222. Factor X deficiency -- Tokyo
     A rare inherited blood clotting disorder where there is a deficiency of a protein (Factor X) which is needed for the blood to clot properly. The Tokyo variant results in reduced Factor X blood clotting activity....more »
    223. Factor X deficiency -- Vorarlberg
     A rare inherited blood clotting disorder where there is a deficiency of a protein (Factor X) which is needed for the blood to clot properly. The Vorarlberg variant results in reduced Factor X blood clotting activity....more »
    224. Factor X deficiency -- Wenatchee I
     A rare inherited blood clotting disorder where there is a deficiency of a protein (Factor X) which is needed for the blood to clot properly. The Wenatchee I variant results in reduced Factor X blood clotting activity....more »
    225. Factor X deficiency -- Wenatchee II
     A rare inherited blood clotting disorder where there is a deficiency of a protein (Factor X) which is needed for the blood to clot properly. The Wenatchee II variant results in reduced Factor X blood clotting activity....more »
    226. Factor X deficiency -- autosomal dominant
     A rare inherited blood clotting disorder where there is a deficiency of a protein (Factor X) which is needed for the blood to clot properly. The autosomal dominant variant results in reduced Factor X blood clotting activity....more »
    227. Factor XIII Deficiency
     A very rare inherited or acquired blood disorder caused by a deficiency of Factor XIII which is involved in stabilizing blood clot formation. The condition manifests as bleeding problems....more »
    228. Factor XIII deficiency, congenital
     A very rare inherited blood disorder caused by a deficiency of Factor XIII which is involved in stabilizing blood clot formation. The condition manifests as bleeding problems....more »
    229. Factor XIII, A1 subunit Deficiency
     A very rare inherited or acquired blood disorder caused by a deficiency of subunit A of Factor XIII which is involved in stabilizing blood clot formation. The condition manifests as bleeding problems....more »
    230. Factor XIII, B subunit Deficiency
     A very rare inherited or acquired blood disorder caused by a deficiency of subunit B of Factor XIII which is involved in stabilizing blood clot formation. The condition manifests as bleeding problems....more »
    231. Fallopian tube cancer
     A cancer that originates in the fallopian tubes which form part of the female reproductive organs. This type of cancer is relatively uncommon....more »
    232. Fallopian tube conditions
     Conditions that affect the fallopian tubes of a woman...more »
    233. Familial hypopituitarism
     Impaired pituitary gland hormone-producing activity that tends to run in families. The failure of the pituitary gland in turn affects other hormone-producing glands which rely on the hormones from the pituitary gland for their activity. Symptoms are deter...more »
    234. Fechtner syndrome
     A rare condition characterized by the presence of large blood platelets, kidney inflammation, deafness and abnormal leukocytes....more »
    235. Female genital disorders
     Any condition affecting the female genital organs....more »
    236. Female genital organ tumors
     Tumors affecting the female genital organs, whether cancerous or bening....more »
    237. Female infertility
     Infertility that affects the female...more »
    238. Female pseudohermaphrodism -- anorectal anomalies
     A very rare disorder characterized by ambiguous external genitals and anal and rectal anomalies....more »
    239. Female reproductive toxicity -- Dioxins
     There is limited conflicting evidence which indicates that some women exposed to dioxins may suffer adverse effects as a result. Spontaneous abortion and menstrual disorders and birth defects are the possible adverse effects....more »
    240. Female reproductive toxicity -- antineoplastic drugs
     There is some evidence which indicates that some women exposed to anticancer drugs may suffer adverse effects as a result. The exposure may occur through the obvious route of having to take the drug to treat cancer but may also inadvertently occur in work...more »
    241. Female sexual conditions
     Sexual conditions that affect the female...more »
    242. Fistula
     The abnormal passage between two internal organs...more »
    243. Fitz-Hugh-Curtis syndrome
     A rare condition where the thin layer around the liver becomes infected as a result of a spread of infection from gonococcal or chlamydial infections in females....more »
    244. Florid cystic endosalpingiosis of the uterus
     Benign tumor-like uterine cysts....more »
    245. Flu
     Very common viral respiratory infection....more »
    246. Forbes-Albright syndrome
     A rare condition where a hormone secreting pituitary or hypothalamic tumor causes galactorrhea and amenorrhea....more »
    247. Fowler-Christmas-Chapple syndrome
     A rare syndrome characterized by the association of polycystic ovaries with the abnormal functioning of the urinary valve....more »
    248. Fragile-X Syndrome
     A rare inherited characterized by various physical anomalies as well as mental retardation. The symptoms are milder in females....more »
    249. Fraser Syndrome
     A rare disorder characterized by the absence of one or both eyes as well as any of a number of other possible congenital abnormalities. Up to half of cases are stillborn....more »
    250. Fraser-like syndrome
     A very rare syndrome characterized by fused eyelids, airway anomalies, cysts in the ovaries and finger and toe abnormalities....more »
    251. Fryns Syndrome
     A rare genetic disorder characterized by diaphragmatic abnormalities, coarse face and abnormal growth or development of ends of fingers and toes....more »
    252. Functioning pancreatic endocrine tumor
     Tumors that develop in the pancreas and cause excessive secretion of one or more pancreatic hormones such as insulin, somatostatin, glucagons, gastrin, ACTH (corticosteroids) and vasoactive intestinal peptidase....more »
    253. GAPO syndrome
     A rare condition characterized by retarded growth, alopecia, otpic atrophy and failure of teeth to erupt....more »
    254. Galactorrhea
     Abnormal breast milk production...more »
    255. Galactorrhoea-Hyperprolactinaemia
     Increased blood prolactin levels associated with galactorrhea (abnormal milk secretion). It may be caused by such things as certain medications, pituitary disorders and thyroid disorders. The condition can occur in males as well as females....more »
    256. Gardner-Morrisson-Abbot syndrome
     A rare syndrome characterized by thrombocytopenia and various other abnormalities present at birth....more »
    257. Generalized anxiety disorder
     Excessive anxiety and worrying....more »
    258. Genital herpes
     Sexually transmitted infection of the genital region....more »
    259. German syndrome
     A rare disorder caused by fetal exposure to trimethadione (anticonvulsant drug) and resulting in various physical and developemental abnormalities....more »
    260. Gestational trophoblastic tumor
     A rare tumor that develops in the uterus from cells formed after an abnormal conception (abnormal union of sperm and egg cell). Gestational trophoblastic tumors can also develop from a normal placenta. There are two type of gestational trophoblastic tumor...more »
    261. Gigantism
     A rare endocrine disorder where excess growth hormone is produced prior to puberty....more »
    262. Glassy cell carcinoma of the cervix
     A rare type of cervical cancer....more »
    263. Gonadal dysgenesis
     The abnormal development of gonads which means that the sex hormones are not being produced. The gonads are the primary reproductive organs - testes in males and ovaries in females. These organs produced sperm and eggs as well as sex hormones - testes pro...more »
    264. Gonadal dysgenesis Turner type
     The abnormal development of gonads that occurs in Turner syndrome due to a chromosomal abnormality. It occurs when the there is only one fully functioning X chromosome instead of two which results in underdeveloped female characteristics. The severity of ...more »
    265. Gonadal dysgenesis mixed
     A rare condition where the testes develop abnormally with asymmetrical gonads as well as sex chromosome abnormalities. The physical manifestations may range from development of female genitalia to male genitalia with hypospadias....more »
    266. Gonadal dysgenesis, XX type
     A rare genetic condition involving non-functional ovaries causing a failure of puberty due to the lack of production of sex hormones by the ovaries....more »
    267. Gonorrhea
     Common sexually transmitted disease often without symptoms....more »
    268. Granuloma inguinale
     Granulomous disease spread sexually....more »
    269. Graves Disease
     is an autoimmune disease characterized by hyperthyroidism due to circulating autoantibodies. Thyroid-stimulating immunoglobulins (TSIs) bind to and activate thyrotropin receptors, causing the thyroid gland to grow and the thyroid follicles to increase syn...more »
    270. Gynaecological conditions
     Any condition the affects the female reproductive organs...more »
    271. Gynandroblastoma
     A type of ovarian tumor that causes feminizing and masculinizing effects of estrogen and androgen....more »
    272. HAIR-AN Syndrome
     A very rare syndrome that affects females only and is characterized mainly by insulin resistance, dark velvety patches of skin and increased male hormone production in females....more »
    273. HIV-1, CRF36_cpx
     HIV is an immune system disease caused by the HIV virus. AIDS is a term used when a person infected with HIV has a CD4+ T cell count below 200 or 14% of lymphocytes. AIDS is an advanced form of HIV. To be classified as AIDS the person must also have an AI...more »
    274. Habitual abortion
     The occurrence of two or more spontaneous abortions in a row. The condition may result from severe fetal abnormality, endocrine disorders, severe kidney problems, structural defects of the cervix or uterus or immune problems....more »
    275. Halal Setton Wang syndrome
     A very rare syndrome characterized mainly by eye, teeth, nail and skin abnormalities....more »
    276. Hemophilia
     Blood disease usually genetic causing failure to clot....more »
    277. Hemorrhagic thrombocythemia
     A rare blood disorder characterized by increased number of platelets in the blood which often results in an enlarged spleen, bleeding and blood vessel blockages....more »
    278. Hepatocellular carcinoma (fibrolamellar variant)
     A rare form of liver cancer. The prognosis for this variant of hepatocellular cancer is better than for hepatocellular cancer....more »
    279. Herbal Agent overdose -- Cottonseed
     Cottonseed can be used as a herbal agent used to reduce male fertility in China. The herbal agent contains a chemical called gossyphol which can cause various overdose symptoms if ingested in excessive quantities....more »
    280. Hereditary Leiomyomatosis and Renal Cell Cancer
     A rare inherited condition characterized by the presence of tumors that develop from smooth muscle tissue in the skin, uterus and the kidneys. The skin anomalies can occur on any part of the body and gradually increase in number and size with age. Kidney ...more »
    281. Hereditary hemorrhagic telangiectasia
     A rare genetic disorder characterized by epistaxes and multiple telangiectases....more »
    282. Hereditary hypothyroidism
     Hereditary hypothyroidism is a condition in which there is a defect in the thyroid gland which leads to increased production of TSH reduced production of thyroid hormone....more »
    283. Human Papillomavirus
     Very common sexually transmitted disease causing genital warts and associated with certain cancers....more »
    284. Human carcinogen -- Infection with Human papillomavirus type 16
     Infection with Human papillomavirus type 16 is deemed to be carcinogenic to humans. Infection with the virus does not mean the patient will definitely develop cancer but the risk of cancer is increased....more »
    285. Human carcinogen -- Infection with Human papillomavirus type 18
     Infection with Human papillomavirus type 18 is deemed to be carcinogenic to humans. Infection with the virus does not mean the patient will definitely develop cancer but the risk of cancer is increased....more »
    286. Human carcinogen -- Infection with Human papillomavirus type 31
     Infection with Human papillomavirus type 31 is deemed to be carcinogenic to humans. Infection with the virus does not mean the patient will definitely develop cancer but the risk of cancer is increased....more »
    287. Human carcinogen -- Infection with Human papillomavirus type 35
     Infection with Human papillomavirus type 35 is deemed to be carcinogenic to humans. Infection with the virus does not mean the patient will definitely develop cancer but the risk of cancer is increased....more »
    288. Human carcinogen -- Infection with Human papillomavirus type 39
     Infection with Human papillomavirus type 39 is deemed to be carcinogenic to humans. Infection with the virus does not mean the patient will definitely develop cancer but the risk of cancer is increased....more »
    289. Human carcinogen -- Infection with Human papillomavirus type 45
     Infection with Human papillomavirus type 45 is deemed to be carcinogenic to humans. Infection with the virus does not mean the patient will definitely develop cancer but the risk of cancer is increased....more »
    290. Human carcinogen -- Infection with Human papillomavirus type 51
     Infection with Human papillomavirus type 51 is deemed to be carcinogenic to humans. Infection with the virus does not mean the patient will definitely develop cancer but the risk of cancer is increased....more »
    291. Human carcinogen -- Infection with Human papillomavirus type 52
     Infection with Human papillomavirus type 52 is deemed to be carcinogenic to humans. Infection with the virus does not mean the patient will definitely develop cancer but the risk of cancer is increased....more »
    292. Human carcinogen -- Infection with Human papillomavirus type 56
     Infection with Human papillomavirus type 56 is deemed to be carcinogenic to humans. Infection with the virus does not mean the patient will definitely develop cancer but the risk of cancer is increased....more »
    293. Human carcinogen -- Infection with Human papillomavirus type 58
     Infection with Human papillomavirus type 58 is deemed to be carcinogenic to humans. Infection with the virus does not mean the patient will definitely develop cancer but the risk of cancer is increased....more »
    294. Human carcinogen -- Infection with Human papillomavirus type 59
     Infection with Human papillomavirus type 59 is deemed to be carcinogenic to humans. Infection with the virus does not mean the patient will definitely develop cancer but the risk of cancer is increased....more »
    295. Human carcinogen -- Infection with Human papillomavirus type 66
     Infection with Human papillomavirus type 66 is deemed to be carcinogenic to humans. Infection with the virus does not mean the patient will definitely develop cancer but the risk of cancer is increased....more »
    296. Hydatidiform mole
     A rare condition where an abnormal union between an egg and a sperm results in the formation of grape-like cysts instead of a baby. The growth is not malignant....more »
    297. Hyperadrenalism
     Excessive levels of adrenal hormones in the body. Symptoms depend on which hormone is involved and the degree of involvement. Adrenal hormones are aldosterone, corticosteroids, androgenic steroids, epinephrine and norepinephrine....more »
    298. Hypergonadotropic ovarian failure
     Premature onset of menopause - occurs before the fourth decade -average age of onset of menopause is about 50 years of age. The condition can occur sporadically or may be inherited in a familial manner....more »
    299. Hypergonadotropic ovarian failure, familial or sporadic
     A rare disorder where the ovaries fail to function prematurely. Ovarian failure can occur in the 20's or 30's. Normal ovarian failure occurs during menopause. Premature ovarian failure can be caused by a genetic mutation and can occur sporadically or in a...more »
    300. Hyperprolactinemia
     High levels of prolactin in the blood....more »
    301. Hypersecretion of growth hormone
    302. Hyperthyroidism -- Teratogenic Agent
     There is strong evidence to indicate that the development of hyperthyroidism during pregnancy may have a teratogenic effect on the fetus. A teratogen is a substance that can cause birth defects. The likelihood and severity of defects may be affected by th...more »
    303. Hypogonadism -- retinitis pigmentosa
     A very rare syndrome characterized by eye disease (retinal pigmentosa) and the absence of puberty caused by a deficiency of hormones that stimulate the sex organs (gonads) into producing the hormones that initiate puberty....more »
    304. Hypothyroid goitre
     Goitre is the enlargement of the thyroid gland and hypothyroid state is characterized by increased TSH levels and decreased T3 and T4 levels circulating in the body....more »
    305. Ichthyosis male hypogonadism
     A very rare syndrome characterized mainly by scaly skin and insufficient hormone production by the male gonads....more »
    306. Imperforate hymen
     Lack of opening in the vaginal hymen...more »
    307. Inflammatory pelvic pain
     Inflammatory pelvic pain can be chr, cyclic,non cyclic, localized of generalized, or a combination. It affects women of reproductive age and older. It's important to note that sudden, severe pain with mass indicates a serious disorder such as an ectopic p...more »
    308. Interstitial cystitis
     A rare condition involving inflammatory disease of the bladder which progresses slowly....more »
    309. Kallmann Syndrome
     A rare inherited condition characterized by hypogonadism, eunuchoidism and impaired or absent sense of smell. The condition occurs as a result of failure of a part of the hypothalamus which results in hormonal imbalance....more »
    310. Kallmann Syndrome 5
     A rare inherited condition characterized by hypogonadism, eunuchoidism and impaired or absent sense of smell. The condition occurs as a result of failure of a part of the hypothalamus which results in hormonal imbalance. The symptoms and their severity ma...more »
    311. Kallmann Syndrome 6
     A rare inherited condition characterized by hypogonadism, eunuchoidism and impaired or absent sense of smell. The condition occurs as a result of failure of a part of the hypothalamus which results in hormonal imbalance. The symptoms and their severity ma...more »
    312. Kallmann syndrome 2
     A rare inherited condition characterized by hypogonadism and impaired or absent sense of smell. The condition occurs as a result of failure of a part of the hypothalamus which results in hormonal imbalance. Type 2 is caused by a genetic defect located at ...more »
    313. Kallmann syndrome, type 1, X-linked
     A rare inherited condition characterized by hypogonadism and impaired or absent sense of smell. The condition occurs as a result of failure of a part of the hypothalamus which results in hormonal imbalance. Type 1 is caused by a genetic defect located at ...more »
    314. Kallmann syndrome, type 3, recessive
     A rare inherited condition characterized by hypogonadism and impaired or absent sense of smell. The condition occurs as a result of failure of a part of the hypothalamus which results in hormonal imbalance. Type 3 is recessively inherited and the genetic ...more »
    315. Kallmann syndrome, type 4
     A rare inherited condition characterized by hypogonadism and impaired or absent sense of smell. The condition occurs as a result of failure of a part of the hypothalamus which results in hormonal imbalance. Type 4 is caused by a genetic defect located at ...more »
    316. Lactotroph adenoma
     A benign pituitary tumor that secretes excessive prolactin which can affect the functioning of the reproductive system - testes and ovaries. The tumor may also grow large enough to compress adjacent structures such as the eye nerves....more »
    317. Laron syndrome type 1
     Laron syndrome is a rare genetic disease where the body has sufficient growth hormones but lacks receptors to utilize the hormone and hence dwarfism results. Type 1 involves a defect in the growth hormone receptor gene which prevents the hormone from bind...more »
    318. Laron syndrome type 2
     Laron syndrome is a rare genetic disease where the body has sufficient growth hormones but lacks receptors to utilize the hormone and hence dwarfism results. Type 1 involves a defect in the growth hormone receptor gene which prevents the hormone from bind...more »
    319. Laron-type dwarfism
     A rare genetic disease where the body has sufficient growth hormones but lacks receptors to utilize the hormone and hence dwarfism results....more »
    320. Laurence-Moon Syndrome
     A rare inherited disorder characterized by vision loss, impaired hormone production, mental retardation and spastic paraplegia....more »
    321. Leiomyomatosis, Esophagogastric and Vulvar
     A rare condition where a tumor develops in the esophagus and vulva. The condition appears to be inherited in an autosomal dominant manner....more »
    322. Leukemia
     Cancer of the blood cells, usually white blood cells....more »
    323. Leukemia, Myeloid
     A form of blood cancer that causes a proliferation of the precursors or immature red blood cells, platelets and certain white blood cells such as granulocytes and monocytes....more »
    324. Leukemia, Myeloid, Aggressive-Phase
     Myeloid leukemia is a form of cancer where the bone marrow makes too many myeloid cells (granulocytes and their precursors) in the bone marrow which accumulates in the blood and eventually invades various parts of the body. The aggressive phase of myeloid...more »
    325. Lichen planus
     Skin rash...more »
    326. Lichen sclerosis et atrophicus
     A chronic skin disease characterized by shiny, white atrophic skin patches which tend to occur on the neck, genital areas, around the anus, under the breasts and in body folds....more »
    327. Lichen simplex chronicus
     Lichen simplex chronicus refers to thickened itchy skin that results from persistently rubbing or scratching an area of skin....more »
    328. Lipodystrophy, familial partial, type 3 (FPLD3)
     A rare metabolic disorder involving abnormal fat gradually disappears from the limbs, trunk and buttocks but stays the same or accumulates on areas such as the face, shoulders, neck and genitals....more »
    329. Lundberg II syndrome
     A rare syndrome involving cataracts, reduced hormone production by ovaries or testes and myopathy which mainly involves the facial and muscles close to the trunk....more »
    330. Lymphogranuloma venereum
     Type of chlamydia (sexually transmitted disease)...more »
    331. Lymphomatous thyroiditis
     Progressive thyroid gland enlargement due to autoimmune disease....more »
    332. Malaria
     A parasitic disease transmitted through mosquito bites....more »
    333. Male reproductive toxicity -- Benzene
     Exposure to Benzene, a recognized reproductive toxicant, can negatively affect the male reproductive system. Benzene is a widely used chemical - in pesticides and as a solvent in industries such as pesticide manufacturing, laboratory chemicals, printing, ...more »
    334. Malignant mixed Mullerian tumor
     A rare malignant cancer that develops in the uterus, ovary or fallopian tubes. The tumor contains epithelial and stromal cells. The cancer may be slow-growing or aggressive and may metastasize....more »
    335. Marijuana abuse
     Illicit depressant/hallucinogenic drug...more »
    336. Martsolf syndrome
     A rare inherited condition characterized by mental retardation, cataracts, small head and hypogonadism (reduced production of hormones by ovaries or testes)....more »
    337. Masculinisation
     Increased male physical appearance in females...more »
    338. May-Hegglin Anomaly
     A rare inherited blood disorder involving abnormalities in some of the blood components (platelets and certain leukocytes). Some patients develop bleeding problems whereas other remain asymptomatic....more »
    339. May-Hegglin thrombocytopenia
     A rare inherited blood disorder involving abnormalities in some of the blood components (platelets and certain leukocytes). Some patients develop bleeding problems whereas other remain asymptomatic....more »
    340. McCune-Albright Syndrome
     A rare genetic multisystem disorder characterized by abnormal skin pigmentation and endocrine gland dysfunction and replacement of parts of bone tissue with fibrous material....more »
    341. Measles
     Once common viral infection now rare due to vaccination....more »
    342. Menopause
     The end of female menstruation and fertility....more »
    343. Menorrhagia
     Excessive menstrual bleeding...more »
    344. Menstrual conditions
     Any condition that is associated with the female menstrual cycle...more »
    345. Menstruation
     The passage of blood and uterine tissue through the vagina cyclically...more »
    346. Miscarriage
     Loss of fetus without human interference...more »
    347. Misoprostol -- Teratogenic Agent
     There is evidence to indicate that exposure to Misoprostol during pregnancy may have a teratogenic effect on the fetus. A teratogen is a substance that can cause birth defects. The likelihood and severity of defects may be affected by the level of exposur...more »
    348. Mittelschmerz
     Mid-cycle abdominal pain due to ovulation...more »
    349. Mullerian aplasia
     A birth defect involving the absence of the uterus, cervix and top part of the vagina but normal external genitals and ovarian function. Secondary sexual characteristics generally develop normally but menstruation is absent....more »
    350. Multiple endocrine neoplasia type 1
     Rare inherited disease causing tumors in multiple glands...more »
    351. Myoma (fibroid)
     A benign tumour of the muscle in the wall of the uterus....more »
    352. Neuroendocrine carcinoma of the cervix
     A rare form of cervical cancer which tends to be quite aggressive....more »
    353. Neurosarcoidosis
     A rare disorder involving sarcoidosis of the nervous system. Sarcoidosis is a chronic inflammatory disorder that can affect virtually any part of the body. Neurosarcoidosis involves inflammation and abnormal deposits in parts of the nervous system includi...more »
    354. Nicotine addiction
     Nicotine addiction is the uncontrollable desire to continue smoking. Smoking products contain nicotine which is a chemical that can lead to addiction if used over a period of time. Cessation causes withdrawal symptoms which can vary in nature and severity...more »
    355. Non Classic Congenital Adrenal Hyperplasia
     A late onset form of congenital adrenal hyperplasia where insufficient adrenal corticosteroids are produced by the body due to the deficiency of a particular chemical. The severity of symptoms varies from person to person and onset may occur as early as c...more »
    356. Non-Specific Urethritis
     Urethral infection usually sexually transmitted...more »
    357. Nonspecific genitourinary infections
     A condition which is characterized by a genitourinary infection like symptoms without a specific cause being found...more »
    358. OHSS
     Excessive stimulation of the ovaries that usually occurs as a complication of in vitro fertilization but may also occur spontaneously. The degree of excessive ovarian stimulation may vary from mild to severe....more »
    359. Obstructive biliary disease
     A disease process that causes obstruction or blockage in one of the bile ducts which are vessels that carry bile from the liver to the digestive system or gallbladder. Diseases that can cause such obstructions includes tumors, gallstones, parasites, bile ...more »
    360. Ovarian Cancer
     Cancer of the ovaries....more »
    361. Ovarian carcinosarcoma
     A type of ovarian cancer....more »
    362. Ovarian cysts
     Cysts occurring in the ovaries....more »
    363. Ovarian insufficiency due to FSH resistance
     A rare disorder where the ovaries fail to function normally as they are unable to respond to follicle stimulating hormones....more »
    364. Ovarian insufficiency, familial
     A rare inherited disorder where the ovaries fail to function normally despite normal levels of hormones that stimulate ovarian activity. Ovarian failure is a normal phase of aging and is associated with menopause but it is termed ovarian insufficiency whe...more »
    365. Ovarioleukodystrophy
     A rare syndrome characterized by ovarian failure and degeneration of the brain white matter which causes mental and motor problems....more »
    366. Ovary conditions
     Any condition that affects a female ovary...more »
    367. Owren Parahemophilia
     An inherited disorder where the deficiency of a blood component affects its ability to clot properly which can lead to bleeding problems. The severity of the disorder can vary from easy bruising to life-threatening hemorrhages....more »
    368. Panhypopituitarism
     A rare condition where all pituitary hormones are absent or reduced. The condition may be congenital or acquired through such things as pituitary tumors. The pituitary gland regulates the activity of other endocrine glands as well as controlling growth. O...more »
    369. Panic attack
     Sudden attack of unreasonable panic or fear without any real danger...more »
    370. Partial 7p Monosomy
     A rare chromosomal disorder where part of the short arm (p) of chromosome 7 is deleted resulting in various abnormalities which are determined by the size and location of the deleted portion....more »
    371. Pelvic Cancer
     Any malignancy that is located in the anatomical location of the pelvis...more »
    372. Pelvic Inflammatory Disease
     Infection of the womb and fallopian tubes....more »
    373. Pelvic inflammatory disease like symptoms
     The main symptoms of pelvic inflammatory disease include diarrhoea, fever and abdominal pain....more »
    374. Pelvis conditions
     Any condition that affects the pelvis...more »
    375. Perimenopause
     The start of onset of menopause...more »
    376. Peritoneum cancer
     A condition that is characterised by the location of a malignant lesion in the perineum...more »
    377. Peritoneum disorders
     Any condition that affects the peritoneum...more »
    378. Persistent sexual arousal syndrome
     A sexual disorder where genital arousal in females continues even though there is no real interest in sex. Patients can find the condition very traumatic as even orgasm does nothing to alleviate the symptoms....more »
    379. Phenprocoumon -- Teratogenic Agent
     There is evidence to indicate that exposure to Phenprocoumon during pregnancy may have a teratogenic effect on the fetus. A teratogen is a substance that can cause birth defects. The likelihood and severity of defects may be affected by the level of expos...more »
    380. Pinworm
     Small, threadlike parasitic worms mainly in colon and rectum...more »
    381. Pituitary Cancer
     Cancer of the pituitary gland....more »
    382. Pituitary cancer, childhood
     Cancer (malignant) of the pituitary gland in children. The pituitary gland produces various hormones and some pituitary tumors (functioning tumors) can affect the secretion of one or more of these hormones resulting in a range of symptoms depending on the...more »
    383. Pituitary tumors, adult
     A benign or cancer tumor that develops in the tissue of the pituitary gland in adults. The pituitary gland produces various hormones and some pituitary tumors (functioning tumors) can affect the secretion of one or more of these hormones resulting in a ra...more »
    384. Placenta previa
     Misplaced placenta covering the cervix...more »
    385. Placental-site gestational trophoblastic tumor
     A rare condition where cancer develops in the uterine muscle and in the site that the placenta was attached. The tumor forms after ectopic pregnancies, abortions or even following a normal delivery....more »
    386. Plasminogen activitor inhibitor type 1 deficiency, congenital
     A rare disorder where a deficiency of a protein results in mild bleeding problems. Though the bleeding disorder is mild, minor trauma can result in excessive bleeding....more »
    387. Polycystic ovarian disease, familial
     A rare familial condition characterized by menstrual abnormalities, excessive growth of hair, obesity and infertility....more »
    388. Polycystic ovaries urethral sphincter dysfunction
     A rare syndrome characterized by the association of polycystic ovaries with the abnormal functioning of the urinary valve....more »
    389. Polycystic ovary syndrome
     Polycystic ovary syndrome (PCOS) is an endocrine disorder that affects approximately 5% of all women....more »
    390. Polydactyly -- myopia syndrome
     A very rare syndrome characterized mainly by extra fingers and toes as well as progressive nearsightedness....more »
    391. Polyembryoma
     An aggressive type of tumor that develops from germ cells. It occurs mainly in the ovaries but sometimes in the testes....more »
    392. Polyp
     An growth or protrusion that extends from a mucous membrane...more »
    393. Prader-Willi syndrome
     A rare genetic disorder characterized by reduced muscle tone, obesity and small hands and feet....more »
    394. Pregnancy
     The condition of supporting a fetus from conception till birth....more »
    395. Premature Ovarian Failure 1
     A condition where menopause occurs earlier than normal due to premature loss of function of the ovaries. Premature menopause refers to menopause occurring before the age of 40 years with the average age of menopause occurring about the age of 50 years. Ty...more »
    396. Premature Ovarian Failure 2
     A condition where menopause occurs earlier than normal due to premature loss of function of the ovaries. Premature menopause refers to menopause occurring before the age of 40 years with the average age of menopause occurring about the age of 50 years. Ty...more »
    397. Premature Ovarian Failure 2A
     A condition where menopause occurs earlier than normal due to premature loss of function of the ovaries. Premature menopause refers to menopause occurring before the age of 40 years with the average age of menopause occurring about the age of 50 years. Ty...more »
    398. Premature Ovarian Failure 2B
     A condition where menopause occurs earlier than normal due to premature loss of function of the ovaries. Premature menopause refers to menopause occurring before the age of 40 years with the average age of menopause occurring about the age of 50 years. Ty...more »
    399. Premature Ovarian Failure 3
     A condition where menopause occurs earlier than normal due to premature loss of function of the ovaries. Premature menopause refers to menopause occurring before the age of 40 years with the average age of menopause occurring about the age of 50 years. Ty...more »
    400. Premature Ovarian Failure 4
     A condition where menopause occurs earlier than normal due to premature loss of function of the ovaries. Premature menopause refers to menopause occurring before the age of 40 years with the average age of menopause occurring about the age of 50 years. Ty...more »
    401. Premature Ovarian Failure 5
     A condition where menopause occurs earlier than normal due to premature loss of function of the ovaries. Premature menopause refers to menopause occurring before the age of 40 years with the average age of menopause occurring about the age of 50 years. Ty...more »
    402. Premature Ovarian Failure 6
     A condition where menopause occurs earlier than normal due to premature loss of function of the ovaries. Premature menopause refers to menopause occurring before the age of 40 years with the average age of menopause occurring about the age of 50 years. Ty...more »
    403. Primary Fallopian Tube Cancer
     A cancer that originates in the fallopian tubes which form part of the female reproductive organs. This type of cancer is relatively uncommon....more »
    404. Primary cortisol resistance
     A rare genetic disorder where the body is unable to respond to a hormone called cortisol. The body produces excess cortisol to compensate for this defect....more »
    405. Primary hypothyroidism
     Primary hypothyroidism is a condition in which a defect in the thyroid gland leads to reduced production of thyroid hormone....more »
    406. Primary malignant melanoma of the cervix
     A form of cervical cancer where the tumor consists of pigment containing cells....more »
    407. Progeria short stature pigmented nevi
     A very rare inherited disorder characterized by premature aging, short stature, and immune system deficiency. The type and severity of symptoms is variable....more »
    408. Prolactinoma, familial
     A pituitary tumor that secretes prolactin and occurs in a familial pattern of inheritance. The tumor is benign but can cause symptoms due to high prolactin levels or compression of the optic nerve....more »
    409. Pseudohermaphrodism -- anorectal anomalies
     A very rare disorder characterized by ambiguous external genitals and anal and rectal anomalies....more »
    410. Pseudohermaphroditism, female -- skeletal anomalies
     A rare disorder characterized by skeletal anomalies and ambiguous female genitals with female gonads....more »
    411. Psoriasis
     Psoriasis is an inflammatory skin condition where the defective immune system causes skin cells to grow rapidly. It affects a significant number of people. Arthritis, which can be severe, is associated with the psoriasis in up to a third of cases. Not all...more »
    412. Puberty
     Sexual and physical maturation in adolescents...more »
    413. Puerperal fever
     Delayed uterine infection after childbirth...more »
    414. Purpura
     Various bruising conditions where small blood vessels hemorrhage...more »
    415. Rectocele
     Rectal prolapse with protrusion into the vagina...more »
    416. Refractory Celiac Disease
     Refractory Celiac Disease is celiac disease that fails to respond to treatment which involves a gluten-free diet. Celiac disease is an autoimmune disorder characterized by intolerance to gluten by the small intestine. The condition is quite uncommon and o...more »
    417. Reiterís syndrome
     A form of reactive arthritis characterized by arthritis, urethritis, conjunctivitis and skin lesions....more »
    418. Renal nutcracker syndrome
     A rare condition where the left renal vein becomes compressed between the abdominal aorta and the superior mesenteric artery. Symptoms usually don't become obvious until the third or fourth decade. The severity of the disorder is variable....more »
    419. Renoanogenital syndrome
     A rare genetic disorder characterized by kidney, anal and genital abnormalities....more »
    420. Reproductive conditions
     Medical conditions of the reproductive system in men or women....more »
    421. Reproductive toxicity -- Xylene (mixed isomers)
     Xylene (mixed isomers) is a suspected reproductive toxicant and exposure to it has the potential to negatively affect the human reproductive system. Xylene (mixed isomers) is used mainly as an industrial solvent and is used in the manufacture paints, lacq...more »
    422. Resistance to LH (luteinizing hormone)
     A genetic abnormality where the body is unable to respond to luteinizing hormone which affects ovarian and testicular function....more »
    423. Resistance to thyroid stimulating hormone
     A very rare disorder where the body is unable to respond to thyroid stimulating hormone even though it is present in sufficient quantities. The problem lies in defective thyroid stimulating hormone receptors....more »
    424. Retinitis pigmentosa, deafness, mental retardation, hypogonadism
     A rare genetic disorder characterized by mental retardation, reduced hormone production by the testes or ovaries, deafness and vision problems....more »
    425. Retroverted uterus
     The tipping back in the position of the uterus in the female pelvis...more »
    426. Rhabdomyosarcoma, Botryoid type
     A type of cancer that arises from rhabdomyoblasts which are immature muscle cells. The tumors can occur arise from muscle tissue almost anywhere in the body but in the Botryoid form, tends to hollow organs with a mucosal lining such as the bladder, uterus...more »
    427. Riedel syndrome
     A rare condition that occurs when fibrous tissue forms in the thyroid area and progressively destroys the thyroid gland....more »
    428. Rud Syndrome
     A condition characterized by ichthyosis, epilepsy, short stature, hypogonadism and severe mental retardation....more »
    429. Sackey-Sakati-Aur syndrome
     A very rare syndrome characterized mainly by a blood disorder and various congenital anomalies such as short stature and a thumb abnormality....more »
    430. Salpingitis
     Inflammation of the fallopian tubes...more »
    431. Sarcoma botryoides
     An aggressive form of cancer that arises from embryonic muscle cells. The tumor resembles a bunch of grapes and tends to occur in the genitourinary tract. Common locations are the cervix, vagina and bladder and very rare cases can occur in the bile duct o...more »
    432. Satoyoshi syndrome
     A very rare syndrome characterized by alopecia, diarrhea, skeletal abnormalities and painful leg cramps caused by physical exercise or emotional stress....more »
    433. Scarlet fever
     A complication of infection from strep bacteria such as strep throat....more »
    434. Schroeder syndrome 1
     High blood pressure and reduced salt concentration in sweat associated with an overactive adrenal cortex which is involved with hormone production....more »
    435. Scurvy
     Severe disease from vitamin C deficiency...more »
    436. Secondary Dysmenorrhea
     Menstrual-like cramping (dysmenorrhea) from an underlying condition....more »
    437. Secondary Fallopian Tube Cancer
     A cancer that originates in some other part of the body and metastasizes to the fallopian tubes which form part of the female reproductive organs. This type of cancer is relatively uncommon....more »
    438. Secondary hypothyroidism
     Secondary hypothyroidism is a condition in which the activity of the thyroid gland is decreased, due to failure of the pituitary gland or hypothalamus...more »
    439. Secondary syphilis
     A condition which is characterized by fever, multiform skin eruptions, iritis, alopecia, mucous patches and severe pain in the head and joints...more »
    440. Semen allergy
     An allergic reaction to the semen of a sexual partner. The reaction may be localized or systemic....more »
    441. Separation anxiety disorder
     Excessive anxiety over separation...more »
    442. Septic abortion
     An abortion associated with a uterine infection. The infection can occur during or just before or after an abortion. The infection can result from factors such as Chlamydia, IUD's or attempted abortion using infected tools....more »
    443. Sertoli-leydig cell tumors
     A rare form of ovarian cancer where excessive male sex hormones are produced by the cancerous cells....more »
    444. Sexual Conditions
     Any condition that affects sexual function...more »
    445. Sexual neuropathy
     Nerve damage resulting in reduced sexual function in men or women...more »
    446. Sexually Transmitted Diseases
     Various diseases spread by sexual contact....more »
    447. Sheehan Syndrome
     A rare condition that occurs in women who suffer a severe uterine hemorrhage during childbirth. The resulting blood loss may damage the pituitary gland and result in hypopituitarism....more »
    448. Sjogren syndrome, primary
     An autoimmune disease where the body's immune system attacks parts of the body that produce moisture such as the eyes, mouth and gastrointestinal tract. Sjogren syndrome can occur on its own (primary) or with another connective tissue disease (secondary) ...more »
    449. Sjogren syndrome, secondary
     An autoimmune disease where the body's immune system attacks parts of the body that produce moisture such as the eyes, mouth and gastrointestinal tract. Sjogren syndrome can occur on its own (primary) or with another connective tissue disease (secondary) ...more »
    450. Sjogren's Syndrome
     Autoimmune disease damaging the eye tear ducts and other glands....more »
    451. Sjogren's syndrome, juvenile, secondary to autoimmune disease
     An autoimmune disorder that affects the glands involved in tear and saliva production as well as gastrointestinal tract moisture. It can occur as a secondary condition associated with other autoimmune disorders such as systemic lupus and rheumatoid arthri...more »
    452. Staphylococcal toxic shock syndrome
     A very rare, potentially fatal infection caused by the bacterial toxins produced by Staphylococcus aureus or Streptococcus pyogenes. The condition is often associated with tampon use but can originate from other sources....more »
    453. Stomach cancer
     Stomach or gastric cancer can develop in any part of the stomach and may spread throughout the stomach and to other organs...more »
    454. Streptococcal Group B invasive disease
     Infection with bacteria called Group B Streptococcus which can cause severe symptoms or even death. The bacteria occur in the stomach and the urogenital tract of females and are normally harmless and cause no symptoms. However, it can cause a range of dis...more »
    455. Stress incontinence
     Stress incontinence is an involuntary loss of urine that occurs during physical activity, such as coughing, sneezing, laughing, or exercise....more »
    456. Stroke
     Serious brain event from bleeding or blood clots....more »
    457. Stuart factor deficiency, acquired
     A rare blood clotting disorder which causes mild to severe bleeding depending on the degree of deficiency of Factor X (Stuart factor). This disorder can be inherited or acquired by people suffering from conditions such as liver disease, amyloidosis, certa...more »
    458. Stuart factor deficiency, congenital
     A rare inherited blood clotting disorder which causes mild to severe bleeding depending on the degree of deficiency of Factor X (Stuart factor)....more »
    459. Susceptibility to Celiac Disease 1
     Susceptibility to celiac disease 1 is a term allocated to a genetic defect on a particular chromosome (chromosome 6p21.3) which makes a patient more susceptible to developing celiac disease. However, it is important to note that having the genetic anomaly...more »
    460. Susceptibility to Celiac Disease 10
     Susceptibility to celiac disease 10 is a term allocated to a genetic defect on a particular chromosome (chromosome 3q25-q26) which makes a patient more susceptible to developing celiac disease. However, it is important to note that having the genetic anom...more »
    461. Susceptibility to Celiac Disease 11
     Susceptibility to celiac disease 11 is a term allocated to a genetic defect on a particular chromosome (chromosome 3q28) which makes a patient more susceptible to developing celiac disease. However, it is important to note that having the genetic anomaly ...more »
    462. Susceptibility to Celiac Disease 12
     Susceptibility to celiac disease 12 is a term allocated to a genetic defect on a particular chromosome (chromosome 6q25) which makes a patient more susceptible to developing celiac disease. However, it is important to note that having the genetic anomaly ...more »
    463. Susceptibility to Celiac Disease 13
     Susceptibility to celiac disease 13 is a term allocated to a genetic defect on a particular chromosome (chromosome 12q24) which makes a patient more susceptible to developing celiac disease. However, it is important to note that having the genetic anomaly...more »
    464. Susceptibility to Celiac Disease 2
     Susceptibility to celiac disease 2 is a term allocated to a genetic defect on a particular chromosome (chromosome 5q31-q33) which makes a patient more susceptible to developing celiac disease. However, it is important to note that having the genetic anoma...more »
    465. Susceptibility to Celiac Disease 3
     Susceptibility to celiac disease 3 is a term allocated to a genetic defect on a particular chromosome (chromosome 2q33) which makes a patient more susceptible to developing celiac disease. However, it is important to note that having the genetic anomaly d...more »
    466. Susceptibility to Celiac Disease 4
     Susceptibility to celiac disease 4 is a term allocated to a genetic defect on a particular chromosome (chromosome 19p13.1) which makes a patient more susceptible to developing celiac disease. However, it is important to note that having the genetic anomal...more »
    467. Susceptibility to Celiac Disease 5
     Susceptibility to celiac disease 5 is a term allocated to a genetic defect on a particular chromosome (chromosome 15q11-q13) which makes a patient more susceptible to developing celiac disease. However, it is important to note that having the genetic anom...more »
    468. Susceptibility to Celiac Disease 6
     Susceptibility to celiac disease 6 is a term allocated to a genetic defect on a particular chromosome (chromosome 4q27) which makes a patient more susceptible to developing celiac disease. However, it is important to note that having the genetic anomaly d...more »
    469. Susceptibility to Celiac Disease 7
     Susceptibility to celiac disease 7 is a term allocated to a genetic defect on a particular chromosome (chromosome 1q133) which makes a patient more susceptible to developing celiac disease. However, it is important to note that having the genetic anomaly ...more »
    470. Susceptibility to Celiac Disease 8
     Susceptibility to celiac disease 8 is a term allocated to a genetic defect on a particular chromosome (chromosome 2q11-q12) which makes a patient more susceptible to developing celiac disease. However, it is important to note that having the genetic anoma...more »
    471. Susceptibility to Celiac Disease 9
     Susceptibility to celiac disease 9 is a term allocated to a genetic defect on a particular chromosome (chromosome 3p21) which makes a patient more susceptible to developing celiac disease. However, it is important to note that having the genetic anomaly d...more »
    472. Syphilis -- Teratogenic Agent
     There is strong evidence to indicate that the development of Syphilis during pregnancy may have a teratogenic effect on the fetus. A teratogen is a substance that can cause birth defects. The likelihood and severity of defects may be affected by the stage...more »
    473. Tertiary hypothyroidism
     Tertiary hypothyroidism results from a malfunction of the hypothalamus, the part of the brain that controls the endocrine system....more »
    474. Tertiary syphilis
     A condition which is characterized by late generalized syphilis with involvement of many organs and tissues...more »
    475. Tetrasomy X
     A rare chromosomal disorder which causes mental retardation, small head and various other anomalies....more »
    476. Thrombasthenia
     An inherited blood clotting disorder where abnormal blood platelet function causes results in excessive bleeding....more »
    477. Thrombocytopathy
     A blood disorder where abnormal blood platelets affect blood coagulation....more »
    478. Thrombocytopenic purpura, autoimmune
     A rare blood disorder where a low number of platelets impairs the bloods ability to clot and results in bleeding into the skin and mucous membranes....more »
    479. Thrush
     Thrush is a fungal infection which is caused by a fungus from the Candida species. It usually affects the mucus membranes of the mouth and vagina. Occasionally the infection can spread throughout the body and cause severe illness....more »
    480. Thyroid disorders
     Any disorder of the thyroid gland....more »
    481. Thyroid hormone plasma membrane transport defect
     Thyroid problems caused by a defect in the transport of a thyroid hormone called T4 (thyroxine) within the body. The thyroid produces excessive hormones to try to compensate for that inability of the body to utilize the hormone....more »
    482. Toe syndactyly, telecanthus, and anogenital and renal malformations
     A rare X-linked syndrome characterized by webbed toes, telecanthus and kidney, genital and anal malformations....more »
    483. Torulopsis
     A type of yeast infection caused by Torulopsis glabrata. The fungus is often found in normal healthy skin, respiratory system, genitourinary system and gastrointestinal system and it generally only becomes a problem in weakened or immunocompromised people...more »
    484. Traumatic Brain Injury
     Brain injury from trauma or accident....more »
    485. Treponema infection
     A rare infectious diseases which is transmitted through sexual contact and caused by Treponema pallidum (a spirochete bacterium). Untreated cases can result in severe complications and even death....more »
    486. Trichomoniasis
     Sexually transmitted parasitic infection....more »
    487. Troell-Junet syndrome
     A disorder involving enlarged extremities, diabetes, skull abnormalities and excessive thyroid hormone production....more »
    488. Trophoblastic Cancer
     A neoplastic disorder that originates in the placenta...more »
    489. Tubal ligation syndrome
     A complication that can occur after sterilization using tubal ligation in females....more »
    490. Tumours related to AIDS
     It usually occurs due to decreased immunity....more »
    491. Turner syndrome associated Celiac Disease
     Females with Turner syndrome are more susceptible to developing celiac disease than the average population. Celiac disease is an autoimmune disorder characterized by intolerance to gluten by the small intestine. The type and severity of symptoms varies am...more »
    492. Type 1 diabetes
     Severe insulin-treated diabetes typically occurring in young people....more »
    493. Type 1 diabetes related Celiac Disease
     Patients with Type 1 diabetes are more susceptible to developing celiac disease than the average population. Celiac disease is an autoimmune disorder characterized by intolerance to gluten by the small intestine. The type and severity of symptoms varies a...more »
    494. Type 2 diabetes
     Most common diabetes in adults, usually progressing slowly, mostly treated without insulin at diagnosis....more »
    495. Typhoid fever
     Fever from bacterial food poisoning....more »
    496. Urethral cancer
     A rare cancer that develops in the urethra which carries urine from the bladder to be excreted....more »
    497. Urinary Incontinence
     Reduced ability to control urine flow....more »
    498. Urogenital dysplasia
    499. Urogenital tumors
     Any tumor of the urinary or genital organs, whether cancerous or benign....more »
    500. Uterine Cancer
     Cancer of the uterus....more »
    501. Uterine fibroids
     Benign nodules in the uterus wall....more »
    502. Uterine prolapse
     Prolapse of the uterus into the wrong position...more »
    503. Uterine sarcoma
     A rare type of cancer that occurs in the uterus or associated tissues. A sarcoma is a cancer that involves soft tissue and connective tissue such as bone, cartilage, fat, muscle and blood vessels....more »
    504. Uterus conditions
     Any condition that affects the female uterus...more »
    505. Vagina cancer
     Cancer of the vagina....more »
    506. Vagina conditions
     Any condition that affects the female vagina...more »
    507. Vaginal Dryness
     Vaginal dryness interfering with sex....more »
    508. Vaginal candidiasis
     Fungal infection of the vagina, sometimes called thrush....more »
    509. Vaginal fistula
     Fistula between vagina and another cavity...more »
    510. Vaginitis
     Vaginal inflammation or infection of any type....more »
    511. Virilising ovarian tumour
     A tumour that results in the virilization of females due to hormone release...more »
    512. Virilism
     Masculinization - enhancement of male secondary sexual characteristics in females such as increased hair growth, deeper voice and baldness....more »
    513. Virilizing ovarian tumor
     An ovarian tumor made up of hormone secreting cells which results in excessive male hormone (androgen) production....more »
    514. Vitamin A embryopathy
     A morbid condition of the embryo caused by the consumption of excess Vitamin A during pregnancy...more »
    515. Vitamin A overdose
     Overdose of Vitamin A usually due to Vitamin A supplement overuse or poisoning....more »
    516. Vohwinkel syndrome
     A rare condition where tight bands of thickened skin form around the base of fingers and toes and generally leads to self-amputation of the digit. Hearing loss is also associated with the condition....more »
    517. Von Willebrand disease
     A rare inherited blood coagulation disorder characterized by a deficiency or defect in plasma protein called the von Willebrand factor which leads to bleeding problems...more »
    518. Von Willebrand disease, dominant form
     A condition that is characterised by autosomal inheritance and is a disorder that is charaterised by prolonged bleeding time....more »
    519. Von Willebrand disease, platelet type
     A condition that is characterised by autosomal inheritance and is a disorder that is charaterised by prolonged bleeding time....more »
    520. Von Willebrand disease, recessive form
     A condition that is characterised by autosomal inheritance and is a disorder that is charaterised by prolonged bleeding time....more »
    521. Von Willebrand disease, type 1
     A rare inherited blood coagulation disorder characterized by a deficiency in plasma protein called the von Willebrand factor which leads to bleeding problems. Most cases of von Willebrand disease are type 1 which is the mildest form of the condition. Pati...more »
    522. Von Willebrand disease, type 2
     A rare inherited blood coagulation disorder characterized by a defect in plasma protein called the von Willebrand factor which leads to bleeding problems. Type 2 is further subdivided into 4 subtypes, each with a different underlying genetic defect. The d...more »
    523. Von Willebrand disease, type 2A
     A rare inherited blood coagulation disorder characterized by a defect in plasma protein called the von Willebrand factor which leads to bleeding problems. Type 2 vWD is further subdivided into 4 subtypes, each with a different underlying genetic defect. T...more »
    524. Von Willebrand disease, type 2B
     A rare inherited blood coagulation disorder characterized by a defect in plasma protein called the von Willebrand factor which leads to bleeding problems. Type 2 vWD is further subdivided into 4 subtypes, each with a different underlying genetic defect. T...more »
    525. Von Willebrand disease, type 2M
     A rare inherited blood coagulation disorder characterized by a defect in plasma protein called the von Willebrand factor which leads to bleeding problems. Type 2 vWD is further subdivided into 4 subtypes, each with a different underlying genetic defect. T...more »
    526. Von Willebrand disease, type 2N
     A rare inherited blood coagulation disorder characterized by a defect in plasma protein called the von Willebrand factor which leads to bleeding problems. Type 2 vWD is further subdivided into 4 subtypes, each with a different underlying genetic defect. T...more »
    527. Von Willebrand disease, type 3
     A rare inherited blood coagulation disorder characterized by a defect in plasma protein called the von Willebrand factor which leads to bleeding problems. Type 3 is the most severe form of von Willebrand Disease....more »
    528. Vulva cancer
     Cancer of the skin of the vulval area....more »
    529. Vulvar Diseases
     Any disease that involves the vulva which is a part of the female genitalia. Diseases can include cancer or fungal, bacterial or viral infections. Symptoms and prognosis will vary depending on the disease process involved....more »
    530. Vulvar vestibulitis syndrome
     The inflammation of the opening of the vagina....more »
    531. Vulvitis
     Vulval skin inflammation...more »
    532. Vulvovaginitis
     Irritation or inflammation of the vulva or vagina. The condition is very common in young girls and can be triggered by moisture, tight clothing, obesity and irritants such as soap....more »
    533. WHIM syndrome
     A rare syndrome characterized by warts, hypogammaglobulinemia (low blood gammaglobulin levels), recurring bacterial infections and myelokathexis (form of neutropenia). It is a form of immunodeficiency disease caused by a mutation in a chemokine receptor....more »
    534. Warfarin -- Teratogenic Agent
     There is evidence to indicate that exposure to Warfarin during pregnancy may have a teratogenic effect on the fetus. A teratogen is a substance that can cause birth defects. The likelihood and severity of defects may be affected by the level of exposure a...more »
    535. Werner syndrome
     A form of premature aging where sufferers start aging during adolescence or soon after and appear old by the time they reach their 30's or 40's. Milder forms of the condition may also occur....more »
    536. Willebrand disease, acquired
     A bleeding disorder characterised by prolonger bleeding time...more »
    537. William's syndrome associated Celiac Disease
     Patients with William's syndrome are more susceptible to developing celiac disease than the average population. Celiac disease is an autoimmune disorder characterized by intolerance to gluten by the small intestine. The type and severity of symptoms varie...more »
    538. Woodhouse Sakati syndrome
     A condition which consists of numerous symptoms such as diabetes, hypogonadism, deafness and mental retardation...more »
    539. XK aprosencephaly
     An extremely rare condition where the forebrain is absent as well as other abnormalities....more »
    540. XX male syndrome
     A sex chromosome disorder in males which affects gonadal development and causes infertility. Males have XX chromosomes instead of the normal XY....more »
    541. XY female
     A person who has a chromosome composition of 46 XY and who is phenotypically female...more »
    542. Xerotic eczema
     Xerotic eczema is a chronic skin condition characterized by very dry patches of skin. The condition is usually triggered by environments which have low humidity such as during winter - this causes the skin to become excessively dry....more »
    543. Y chromosome pericentric inversion
     A genetic abnormality that usually results in the miscarriage of a fetus...more »
    544. Yolk sack tumour
     A germ cell tumour that is a proliferation of yolk sack endoderm...more »
    545. Yusho disease
     A condition that affects the menstrual cycle of female as well as having effects on the immune system...more »
    546. Zadik Barak Levin syndrome
     A condition that affects the endocrine system as well as some facial characteristics...more »

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