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Symptom Checker » Amenorrhea » Asterixes
 

Amenorrhea and Asterixes and Proximal muscle weakness
Symptom Checker

Results: Causes of Amenorrhea AND Asterixes AND Proximal muscle weakness

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

Results: 228 causes of Amenorrhea OR Asterixes OR Proximal muscle weakness

    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?-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 »
    3. 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 »
    4. ACTH -- Teratogenic Agent
     Experimental studies on mice indicate that the use of ACTH during pregnancy may cause various harmful effects on the fetus. The likelihood and severity of symptoms may be affected by the level of exposure and the stage of pregnancy that the exposure occur...more »
    5. Achard-Thiers Syndrome
     A hormonal disorder that occurs in diabetic postmenopausal women. It is characterized by diabetes mellitus and hirsuitism....more »
    6. Acromegaloid, Cutis Verticis Gyrata, Corneal Leukoma Syndrome
     A rare condition characterized by the association of acromegaly, cutis verticis gyrate and corneal leukoma....more »
    7. Acute intermittent porphyria
     A rare metabolic disorder characterized by a deficiency in the porphobilinogen deaminase enzyme which results in a build-up of porphyrins or its precursors in the body. Using certain drugs or eating certain foods can trigger the symptoms of the condition....more »
    8. Addison's Disease
     A rare progressive hormonal disorder characterized by insufficient production of certain hormones called adrenal corticosteroids....more »
    9. 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 »
    10. Adrenal disorders
     Disorders affecting the adrenal glands...more »
    11. Adrenal hyperplasia
     A group of disorder that occur when there is a problem in the process of making adrenal corticosteroids....more »
    12. 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 »
    13. Ahumada-Del Castillo Syndrome
     A rare endocrine disorder characterized by dysfunction of the pituitary and hypothalamus glands in women....more »
    14. Alcoholism
     Alcoholism is the compulsive urge to drink alcohol despite knowing the negative impact on one's health....more »
    15. Ameloblastoma
     A very rare disorder involving the jaw and sinuses. Cyts or tumors which may be malignant form in the jaw, sinus, nose or eye socket areas....more »
    16. Amenorrhea
     Absence of menstrual periods due to many possible causes....more »
    17. Androgen Insensitivity Syndrome
     Females with male XY genetics but inability to respond to testosterone....more »
    18. Anemia
     Reduced ability of blood to carry oxygen from various possible causes....more »
    19. Anorexia
     Any type of appetite loss; often refers to anorexia nervosa...more »
    20. Anorexia Nervosa
     A disorder where a distorted sense of body image leads to self-starvation to the point of death in some cases....more »
    21. Anovulation
     Failure to ovulate...more »
    22. Anxiety
     A feeling of apprehension, and fear without apparent stimulus that is associated sometime with somatic responses...more »
    23. Anxiety disorders
     Anxiety disorders are persistent and excessive feelings of fear, worry or uneasiness that are significant enough to have an impact on day-to-day life. Excessive anxiety can have repercussions on physical and mental health. There are a number of different ...more »
    24. Aromatase deficiency
     A congenital deficiency of the enzyme called aromatase which is needed to convert androgens to estrogens....more »
    25. Asherman's syndrome
     Scarring and adhesions that develop in the uterus and can result in menstrual and fertility problems....more »
    26. 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 »
    27. Autoimmune Hepatitis
     Liver inflammation caused due to autoimmune processes where the body's immune system attacks the liver....more »
    28. 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 »
    29. 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 »
    30. 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 »
    31. Bearn-Kunkel syndrome
     A type of autoimmune liver disease characterized by liver damage, very high blood gammaglobulin levels and increased plasma cells....more »
    32. Blepharophimosis, ptosis, epicanthus inversus
     A rare genetic disorder characterized by inner canthal folds, lateral displacement of inner canthi and drooping upper eyelid....more »
    33. Brain cancer
     Cancer of the brain....more »
    34. Breast Feeding
     Nursing an infant with breast milk....more »
    35. Bulimia nervosa
     Eating disorder with binging (overeating) and purging (vomiting)....more »
    36. CCFDN
     A rare, recessively inherited syndrome characterized by cataracts during infancy, unusual facial appearance and neuropathy....more »
    37. Celiac Disease
     Digestive intolerance to gluten in the diet....more »
    38. 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 »
    39. Chondrodysplasia, acromesomelic, with genital anomalies
     A very rare condition characterized by severe limb malformations and genital anomalies. The reported case involved related parents....more »
    40. 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 »
    41. 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 »
    42. 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 »
    43. 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 »
    44. 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 »
    45. Chronic Illness
     Any form of continuing chronic illness....more »
    46. 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 »
    47. 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 »
    48. Complete androgen insensitivity
    49. 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 »
    50. Congenital hypothyroidism
     A condition in infancy or early childhood due to an in-utero deficiency of thyroid hormones that can be caused by genetic or environmental factors, such as thyroid dysgenesis or hypothyroidism in infants of mothers treated with thiouracil during pregnancy...more »
    51. Conn's syndrome
     An uncommon (but possible highly underdiagnosed) condition characterized by the excessive production of a hormone called aldosterone by the adrenal gland. The condition may result from the presence of an adenoma, carcinoma or enlargement of the adrenal gl...more »
    52. Corticosteroids -- Teratogenic Agent
     There is evidence to indicate that exposure to Corticosteroids 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 exp...more »
    53. Corticotropin -- Teratogenic Agent
     There is evidence to indicate that exposure to Corticotropin 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 »
    54. 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 »
    55. Crohn's disease
     Crohn's disease causes inflammation of the digestive system. It is one of a group of diseases called inflammatory bowel disease. The disease can affect any area from the mouth to the anus. It often affects the lower part of the small intestine called the ...more »
    56. Culler-Jones syndrome
     A very rare syndrome characterized mainly by hypopituitarism (low pituitary hormone level) which affects other hormone levels and an extra little finger....more »
    57. Cushing's disease
    58. 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 »
    59. Cyclophosphamide -- Teratogenic Agent
     There is evidence to indicate that exposure to Cyclophosphamide 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 ex...more »
    60. Depression
     Various syndromes with excessive anxiety, phobias, or fear....more »
    61. Dermatomyositis
     A muscle disease characterized by chronic muscle inflammation resulting in progressive muscle weakness and a characteristic rash....more »
    62. 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 »
    63. 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 »
    64. 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 »
    65. 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 »
    66. Dienestrol -- Teratogenic Agent
     There is evidence to indicate that exposure to Dienestrol (a synthetic form of Viagra) 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 affe...more »
    67. Diethylstilbestrol -- Teratogenic Agent
     There is evidence to indicate that exposure to Diethylstilbestrol (a nonsteroidal estrogen) 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...more »
    68. Dosage-sensitive sex reversal
     A genetic defect resulting in a sex reversal in people with a normal 46,XY karyotype. Thus a genetic male may develop female external genitalia. The severity of the condition is variable with external genitalia ranging from female to ambiguous to male....more »
    69. 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 »
    70. Drash syndrome
     A ver rare disorder involving kidney dysfunction, genital abnormalities and a kidney tumor (Wilm's tumor)....more »
    71. Dystrophia myotonica 1
     A rare genetic disorder characterized by myotonia, muscle atrophy, cataracts and hypogonadism....more »
    72. Eating disorders
     Various mental disorders impairing normal eating or appetite....more »
    73. Ectopic pregnancy
     A condition where a fertilized egg embeds itself outside the uterus....more »
    74. Emotional disorders
     A disorder of emotions...more »
    75. Emotional stress
     A condition which occurs when a person is under stress affecting their emotions...more »
    76. Endocrine disorders
     Any disorder that affects the endocrine system...more »
    77. Ethanol -- Teratogenic Agent
     There is evidence to indicate that exposure to Ethanol 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 an...more »
    78. Excessive dieting
     Excessive limitation of food intake can lead to problems and effects such as dizziness, depression, intestinal problems, edema and impaired growth....more »
    79. Exercise
     The use of the human muscles to improve ones health...more »
    80. FSH-resistant ovaries (FSH-RO)
     A recessively inherited disorder where the ovaries are unable to respond to the follicle stimulating hormone which results in symptoms such as lack of menstruation and infertility....more »
    81. Follicle-stimulating hormone deficiency, isolated
     A genetic disorder characterized by the deficiency of follicle-stimulating hormone which primarily affects fertility....more »
    82. Forbes-Albright syndrome
     A rare condition where a hormone secreting pituitary or hypothalamic tumor causes galactorrhea and amenorrhea....more »
    83. Frasier syndrome
     A rare syndrome involving kidney disease and male pseudohermaphrodism (genetic male with some female sex organs). Kidney failure can occur as early as adolescence....more »
    84. GSD IIB -- formerly
     A rare inherited disorder characterized by severe heart problems, varying degrees of muscle weakness and often mental retardation. Other symptoms such as mental retardation may also occur. The genetic anomaly manifests as a deficiency of a protein called ...more »
    85. GSD2B -- formerly
     A rare inherited disorder characterized by severe heart problems, varying degrees of muscle weakness and often mental retardation. Other symptoms such as mental retardation may also occur. The genetic anomaly manifests as a deficiency of a protein called ...more »
    86. Galactorrhea
     Abnormal breast milk production...more »
    87. 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 »
    88. Glycogen Storage Disease IIb -- formerly
     A rare inherited disorder characterized by severe heart problems, varying degrees of muscle weakness and often mental retardation. Other symptoms such as mental retardation may also occur. The genetic anomaly manifests as a deficiency of a protein called ...more »
    89. Glycogen storage disease type 2B
     A rare inherited biochemical disorder involving the harmful accumulation of certain chemicals (glycogen) in body tissues due to the deficiency of an enzyme (?-glucosidase or acid maltase) needed to break it down. Type IIB usually starts during childhood....more »
    90. Glycogen storage disease type 2B -- formerly
     A rare inherited disorder characterized by severe heart problems, varying degrees of muscle weakness and often mental retardation. Other symptoms such as mental retardation may also occur. The genetic anomaly manifests as a deficiency of a protein called ...more »
    91. 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 »
    92. 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 »
    93. 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 »
    94. Gordan-Overstreet syndrome
     A rare variant of Turner syndrome....more »
    95. 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 »
    96. Grief or loss
     The normal emotional response that occurs to an external loss...more »
    97. Heart failure
     Slow failure of the heart (cardiac insufficiency)....more »
    98. 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 »
    99. 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 »
    100. Hereditary carnitine deficiency syndrome, myopathic
     An inherited deficiency of carnitine in muscles resulting primarily in muscle weakness - generally less severe than the systemic form....more »
    101. Hereditary inclusion body myopathy -- joint contractures -- ophthalmoplegia
     A very rare, dominantly inherited genetic disorder involving progressive muscle weakness and wasting, joint contractures at birth and ophthalmoplegia. Muscle function problems usually don't start until the 4th or 5th decade of life....more »
    102. Hodgkin's Disease
     A form of cancer that affects the lymphatic system....more »
    103. 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 »
    104. 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 »
    105. Hyperparathyroidism
     Increased secretion of parathyroid hormone from the parathyroid glands....more »
    106. Hyperprolactinemia
     High levels of prolactin in the blood....more »
    107. 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 »
    108. Hypoglycemia
     Low blood sugar level...more »
    109. 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 »
    110. Hypogonadism hypogonadotropic due to mutations in GR hormone
     Hypogonadism hypogonadotropic due to mutations in GR hormone is a condition where defects in the gene for gonadotropin-releasing hormone results in problems with sexual maturation during development. The symptoms may vary in severity depending on the degr...more »
    111. Hysterectomy
     The surgical removal of the female uterus...more »
    112. Imperforate hymen
     Lack of opening in the vaginal hymen...more »
    113. Inclusion Body Myositis
     Progressive inflammatory muscle disease causing muscle weakness....more »
    114. Inclusion body myopathy 3, autosomal dominant
     A very rare, dominantly inherited genetic disorder involving progressive muscle weakness and wasting, joint contractures at birth and ophthalmoplegia. Muscle function problems usually don't start until the 4th or 5th decade of life....more »
    115. Inclusion body myopathy associated with Paget disease of bone and frontotemporal dementia
     An inherited muscle wasting disorder associated with dementia and bone disease....more »
    116. Insanity
     A non specific term used to describe a severely deteriorated mental state resulting from a mental disorder....more »
    117. Insulin resistance, short fifth metacarpals
     A rare syndrome characterized by short fifth fingers and fifth hand bones as well as insulin resistance....more »
    118. 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 »
    119. Kidney failure
     Total failure of the kidneys to filter waste...more »
    120. Klotz syndrome
     A rare syndrome characterized mainly by absent menstruation, infantile genitals and other sexual organ abnormalities in females who are genetically male....more »
    121. Kwashiorkor
     A malnutrition state that is produced by severe protein deficiency...more »
    122. 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 »
    123. Lamictal -- Teratogenic Agent
     There is evidence to indicate that exposure to Lamictal 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 »
    124. Lamotrigine -- Teratogenic Agent
     There is evidence to indicate that exposure to Lamotrigine 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 »
    125. 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 »
    126. 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 »
    127. 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 »
    128. Leydig cells hypoplasia
     A condition resulting from reduced or absent functioning of Leydig cells which leads to insufficient production of the male hormone androgen which can cause problems with sex differentiation in males at puberty. The severity of symptoms varies depending o...more »
    129. Leydig cells hypoplasia, type I
     A condition resulting from reduced or absent functioning of Leydig cells which leads to insufficient production of the male hormone androgen which can cause problems with sex differentiation in males at puberty. The severity of symptoms varies depending o...more »
    130. Limb-Girdle muscular dystrophy type 2A
     An autosomal recessive form of limb-girdle muscular dystrophy where muscle weakness and atrophy is caused by mutations of the Calpain-3 gene....more »
    131. Limb-girdle muscular dystrophy type 1C
     An autosomal dominant form of limb-girdle muscular dystrophy where muscle weakness and atrophy is caused by mutations of the Caveolin-3 gene....more »
    132. Limb-girdle muscular dystrophy type 1D
     An autosomal dominant form of limb-girdle muscular dystrophy where muscle weakness and atrophy is caused by mutations of chromosome 6. Males are more severely affected than females in this form of the disease....more »
    133. Limb-girdle muscular dystrophy type 2I
     An autosomal recessive form of limb-girdle muscular dystrophy where muscle weakness and atrophy is caused by mutations of the FKRP (fukutin-related protein) gene....more »
    134. 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 »
    135. Lupus
     Autoimmune disease with numerous effects on various organs and linings....more »
    136. Lysosomal glycogen storage disease with normal acid maltase activity
     A rare inherited disorder characterized by severe heart problems, varying degrees of muscle weakness and often mental retardation. Other symptoms such as mental retardation may also occur. The genetic anomaly manifests as a deficiency of a protein called ...more »
    137. Male pseudohermaphroditism, incomplete hereditary (type 1)
     A rare condition involving a deficiency of dihydrotestosterone receptor which impairs the function of androgen receptors and hence the androgen (male hormone) is partially or completely ineffective depending on the level of deficiency. The degree of femin...more »
    138. Marasmus
     A form of malnutrition caused by a severe deficiency of both protein and calories...more »
    139. Masculinisation
     Increased male physical appearance in females...more »
    140. Menopause
     The end of female menstruation and fertility....more »
    141. Metoclopramide -- Teratogenic Agent
     There is evidence to indicate that exposure to Metoclopramide 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 expo...more »
    142. Michels-Caskey syndrome
     A very rare disorder characterized by underdeveloped thumbs, spine deformities and lack of development of the female reproductive organs such as the uterus and vagina (mullerian duct aplasia). The external genitalia may appear to be normal....more »
    143. Mitochondrial diseases
     Any of a group of mitochondrial disorders affecting cell metabolism and especially muscles....more »
    144. Mosse syndrome
     A condition involving the association of liver cirrhosis with polycythemia which is a chronic myeloproliferative disorder characterized by the excessive production of mainly red blood cells by the bone marrow....more »
    145. 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 »
    146. Multiple endocrine neoplasia type 1
     Rare inherited disease causing tumors in multiple glands...more »
    147. Mumps
     An acute viral disease that causes the salivary glands to become swollen, sore and inflamed. Immunization had greatly reduced the incidence of this disease....more »
    148. Muscular dystrophy, limb-girdle type 2M
     An autosomal recessive form of limb-girdle muscular dystrophy where muscle weakness and atrophy is caused by a defect in the fukutin gene on chromosome 9q31....more »
    149. Muscular dystrophy, limb-girdle, autosomal recessive, type 2K
     An autosomal recessive form of limb-girdle muscular dystrophy where muscle weakness and atrophy is caused by mutations in the gene for O-mannosyltransferase-1....more »
    150. Myotonic Dystrophy
     An inherited disorder characterized by progressive muscle weakness and wasting as well as eye defects, heart abnormalities and other anomalies. The severity of the condition is greatly variable. There are two type of myotonic dystrophy with type 1 being m...more »
    151. Myotonic dystrophy type 3
     A rare genetic disorder characterized by myotonia, muscle atrophy, cataracts and hypogonadism....more »
    152. Myxedema
     Skin and tissue disorder usually due to hypothyroidism...more »
    153. 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 »
    154. Noonan syndrome 3
     A genetic condition characterized by short stature, distinctive facial characteristics, learning difficulties, congenital heart conditions and various other anomalies....more »
    155. Obesity
     An increase in the body weight greater than that required for normal function that is characterised by the accumulation of excessive fat...more »
    156. Obesity due to prohormone convertase-I deficiency
     A form of monogenic obesity caused by a genetic mutation which results in a deficiency of prohormone convertase-I. Monogenic obesity is obesity caused by a mutation in a single gene....more »
    157. Osteomalacia
     A condition where the bones gradually soften and bend due to poor calcification stemming from a lack or impaired metabolism of vitamin D....more »
    158. Ovarian Cancer
     Cancer of the ovaries....more »
    159. Ovarian cysts
     Cysts occurring in the ovaries....more »
    160. 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 »
    161. 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 »
    162. Ovarioleukodystrophy
     A rare syndrome characterized by ovarian failure and degeneration of the brain white matter which causes mental and motor problems....more »
    163. 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 »
    164. Paraneoplastic syndromes
    165. Perimenopause
     The start of onset of menopause...more »
    166. Perphenazine -- Teratogenic Agent
     There is evidence to indicate that exposure to Pentazocine 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 »
    167. Phenytoin -- Teratogenic Agent
     There is evidence to indicate that exposure to Phenytoin 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 »
    168. Pituitary Cancer
     Cancer of the pituitary gland....more »
    169. Pituitary conditions
     Any condition that affects the pituitary...more »
    170. 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 »
    171. Polycystic ovary syndrome
     Polycystic ovary syndrome (PCOS) is an endocrine disorder that affects approximately 5% of all women....more »
    172. Possible human carcinogenic exposure -- Medroxyprogesterone acetate
     Some evidence indicates that exposure to Medroxyprogesterone acetate has a possible link to an increased risk of developing cancer in humans. The carcinogenicity of the substance may be influenced by the duration and level of exposure....more »
    173. Prader-Willi syndrome
     A rare genetic disorder characterized by reduced muscle tone, obesity and small hands and feet....more »
    174. Pregnancy
     The condition of supporting a fetus from conception till birth....more »
    175. Probable human carcinogen -- Anabolic steroids
     Anabolic steroids are a substance deemed to be a probable carcinogen to humans. The carcinogenicity of the substance may be influenced by the duration and level of exposure....more »
    176. 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 »
    177. Pseudoglycogenosis II
     A rare inherited disorder characterized by severe heart problems, varying degrees of muscle weakness and often mental retardation. Other symptoms such as mental retardation may also occur. The genetic anomaly manifests as a deficiency of a protein called ...more »
    178. Pseudohermaphroditism, female -- skeletal anomalies
     A rare disorder characterized by skeletal anomalies and ambiguous female genitals with female gonads....more »
    179. Psychiatric disorders associated Celiac Disease
     Patients with Psychiatric disorders 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 va...more »
    180. 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 »
    181. 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 »
    182. Respiratory failure
     Failure of the respiratory system...more »
    183. Rokitansky-Kuster-Hauser syndrome
     A rare condition characterized by absence of the vagina and uterine abnormalities....more »
    184. Satoyoshi syndrome
     A very rare syndrome characterized by alopecia, diarrhea, skeletal abnormalities and painful leg cramps caused by physical exercise or emotional stress....more »
    185. Scleroderma, systemic
     A rare autoimmune connective tissue disease where the body attacks parts of the body and causes scarring and thickness of the tissue. In the systemic form, the skin and organs are involved....more »
    186. Sertoli-leydig cell tumors
     A rare form of ovarian cancer where excessive male sex hormones are produced by the cancerous cells....more »
    187. 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 »
    188. Spinal Muscular Atrophy
     A rare condition characterized by progressive degeneration of the spinal and brainstem motor neurons. During fetal development excess primary neurons are formed. The body automatically destroys the extra primary neurons so that only some survive and matur...more »
    189. Spinal stenosis
     Narrowing of the spinal cavity around the spinal cord....more »
    190. Spironolactone -- Teratogenic Agent
     There is evidence to indicate that exposure to Spironolactone 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 expo...more »
    191. Stress
     Emotional stress (sometimes refers to physical stress)...more »
    192. 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 »
    193. 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 »
    194. 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 »
    195. 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 »
    196. 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 »
    197. 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 »
    198. 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 »
    199. 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 »
    200. 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 »
    201. 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 »
    202. 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 »
    203. 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 »
    204. 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 »
    205. Swyer syndrome
     A rare disorder where a female has all the normal external femal characteristics but has non-functioning gonads. This means that none sex hormones needed for puberty are produced....more »
    206. Temporal arteritis
     Inflamed head artery causing headache....more »
    207. Tetrasomy X
     A rare chromosomal disorder which causes mental retardation, small head and various other anomalies....more »
    208. Thyroid disorders
     Any disorder of the thyroid gland....more »
    209. Triple-X syndrome
     A condition that is characterised by the occurrence of three X chromosomes...more »
    210. Tubal ligation syndrome
     A complication that can occur after sterilization using tubal ligation in females....more »
    211. Tuberculosis
     Bacterial infection causing nodules forming, most commonly in the lung....more »
    212. Turner Syndrome
     Rare chromosome syndrome with one X but no second X or Y chromosome....more »
    213. 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 »
    214. 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 »
    215. Type 2 diabetes
     Most common diabetes in adults, usually progressing slowly, mostly treated without insulin at diagnosis....more »
    216. Underweight
     Body weight below normal (BMI20)>...more »
    217. Vacuolar Cardiomyopathy and Myopathy, X-linked
     A rare inherited disorder characterized by severe heart problems, varying degrees of muscle weakness and often mental retardation. Other symptoms such as mental retardation may also occur. The genetic anomaly manifests as a deficiency of a protein called ...more »
    218. Vagina, absence of
     A condition characterised by the absence of a vagina at birth...more »
    219. Vasquez Hurst Sotos syndrome
     A rare genetic disorder characterized by underdeveloped genitals, obesity, mental retardation and skeletal abnormalities....more »
    220. Virilizing ovarian tumor
     An ovarian tumor made up of hormone secreting cells which results in excessive male hormone (androgen) production....more »
    221. Vitamin A embryopathy
     A morbid condition of the embryo caused by the consumption of excess Vitamin A during pregnancy...more »
    222. Vitamin D deficiency
     Deficiency of vitamin D...more »
    223. Weight Gain
     An increase in weight for any reason....more »
    224. 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 »
    225. 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 »
    226. Wilson's Disease
     Wilson disease, or hepatolenticular degeneration, is a neurodegenerative disease of copper metabolism....more »
    227. Woodhouse Sakati syndrome
     A condition which consists of numerous symptoms such as diabetes, hypogonadism, deafness and mental retardation...more »
    228. XY female
     A person who has a chromosome composition of 46 XY and who is phenotypically female...more »

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