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Symptom Checker » Easy bruising » Pes planus
 

Easy bruising and Pes planus and Pneumothorax
Symptom Checker

Results: Causes of Easy bruising AND Pes planus AND Pneumothorax

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

Results: 311 causes of Easy bruising OR Pes planus OR Pneumothorax

    1. 49,XXXXY syndrome
     A rare sex chromosome abnormality where there are three extra copies of the X chromosome....more »
    2. ADP platelet receptor P2Y12, deficiency of
     Deficiency of a compound (P2Y12) involved in the blood clotting process which results in bleeding problems....more »
    3. ALL-Down syndrome
     The presence of acute lymphoblastic leukemia in Down syndrome patients. These patients tend to have a poorer prognosis for the leukemia than patients without Down syndrome....more »
    4. ATRUS syndrome
     A rare syndrome characterized by fusion of the forearm bones near the elbow and a blood disorder....more »
    5. Aantibodies anti-FVIIIc syndrome
     A rare, acquired blood condition where the body develops antibodies against a blood clotting factor (FVIII) which results in bleeding problems....more »
    6. Accutane -- Teratogenic Agent
     There is strong evidence to indicate that the use of Accutane 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 level of exp...more »
    7. Achard syndrome
     An inherited connective tissue disorder characterized primarily by a short head, long, slender bones, recessed lower jaw and loose hand and foot joints....more »
    8. Acquired Aplastic Anemia
     A rare disorder involving severe failure of the bone marrow to produce new blood cells. Acquired aplastic anemia means that the condition was not present at birth but developed during the persons lifetime. The condition may be caused by such things as aut...more »
    9. Acquired amegakaryocytic thrombocytopenia
     A rare blood disorder characterized by a deficiency of blood platelets required for normal blood clotting. Autoimmune processes can be a cause of the acquired form of this condition....more »
    10. Acquired hypoprothrombinemia
     A low level of blood prothrombins which is not inherited but occurs as a result of certain medical disorders such as Vitamin K deficiency....more »
    11. 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 »
    12. Acquired pure megakaryocytic aplasia
     A rare blood disorder characterized by severe thrombocytopenia (reduced blood platelets) or reduced megakaryocytes (bone marrow cells that produce blood platelets). The disorder may be caused by immune processes inhibiting the development of megakaryocyte...more »
    13. Acute biphenotypic leukemia
     A rare form of leukemia that has myeloid and lymphoid features....more »
    14. Acute erythroleukemia
     A rare condition characterized by the presence of abnormal blood cells (erythroblastic precursors) in the bone marrow and blood. The condition is characterized by anemia and generally leads to the development of acute myelogenous leukemia. The acute form ...more »
    15. 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 »
    16. Acute leukemia
     An acute condition which affects a cell line of the blood which shows little or no differentiation...more »
    17. Acute lymphoblastic leukemia
     Cancer of the white blood cells. Precursors to white blood cells are called blasts and are made by the bone marrow but in ALL the blasts are abnormal and do not develop into lymphocytes. Instead, the abnormal blasts or leukemic cells multiply rapidly and ...more »
    18. Acute lymphoblastic leukemia, Susceptibility to
     Cancer of the white blood cells characterized by the presence of excessive lymphoblasts. Precursors to white blood cells are called blasts and are made by the bone marrow but in ALL the blasts are abnormal and do not develop into lymphocytes. Instead, the...more »
    19. Acute lymphoblastic leukemia, Susceptibility to, 1
     Cancer of the white blood cells characterized by the presence of excessive lymphoblasts. Precursors to white blood cells are called blasts and are made by the bone marrow but in ALL the blasts are abnormal and do not develop into lymphocytes. Instead, the...more »
    20. Acute lymphoblastic leukemia, Susceptibility to, 2
     Cancer of the white blood cells characterized by the presence of excessive lymphoblasts. Precursors to white blood cells are called blasts and are made by the bone marrow but in ALL the blasts are abnormal and do not develop into lymphocytes. Instead, the...more »
    21. Acute lymphoblastic leukemia, adult
     Cancer of the white blood cells. Precursors to white blood cells are called blasts and are made by the bone marrow but in ALL the blasts are abnormal and do not develop into lymphocytes. Instead, the abnormal blasts or leukemic cells multiply rapidly and ...more »
    22. Acute megacaryoblastic leukemia
     A rare form of malignant bone marrow cancer involving the proliferation of immature precursors of blood cells. More specifically, it involves the rapid proliferation of megakaryoblasts (premature form of megakaryocytes)....more »
    23. Acute mercury inhalation
     Inhalation of mercury vapor can lead to serious symptoms and even death if sufficient quantities are inhaled. Mercury inhalation is more likely in confined or poorly ventilated spaces. Mercury from a broken thermometer can lead to symptoms if it occurs in...more »
    24. Acute myeloblastic leukemia type 1
     A form of blood cancer resulting in the rapid proliferation of immature blood cells (blast cells)....more »
    25. Acute myeloblastic leukemia type 2
     A form of blood cancer resulting in the rapid proliferation of granulocytes and monocytes....more »
    26. 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 »
    27. Acute myeloblastic leukemia type 4
     A rare form of malignant bone marrow cancer involving the rapid proliferation of immature precursors of blood cells. Type 4 involves the rapid proliferation of myelocytes and monocytes....more »
    28. Acute myeloblastic leukemia type 5
     A rare form of malignant bone marrow cancer involving the proliferation of immature precursors of blood cells. Type 5 involves the rapid proliferation of monoblasts (immature precursors of monocytes) in particular....more »
    29. 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 »
    30. Acute myeloblastic leukemia type 7
     A rare form of malignant bone marrow cancer involving the proliferation of immature precursors of blood cells. Type 7 involves the rapid proliferation of megakaryoblasts (premature form of megakaryocytes) in particular....more »
    31. 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 »
    32. 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 »
    33. 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 »
    34. 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 »
    35. 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 »
    36. Acute myeloid leukemia, adult
     A form of blood cancer resulting in the rapid proliferation of granulocytes and monocytes, red blood cells and platelets....more »
    37. 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 »
    38. Adult Cystic Fibrosis
     Cystic fibrosis is an inherited condition characterized by the production of thick sticky mucus by the mucus glands in the lungs, intestines, liver and pancreas. The condition is most often diagnosed in children or young adults but occasionally, relativel...more »
    39. Adult respiratory distress syndrome
     Severe respiratory failure...more »
    40. Aging
     The medical conditions from getting older....more »
    41. Al Gazali Sabrinathan Nair syndrome
     A very rare syndrome characterized by bone and eye problems, seizures and mental retardation....more »
    42. Alcohol-induced pseudo-Cushing syndrome
     The excessive consumption of alcohol can result in symptoms similar to a condition called Cushing's syndrome. When alcohol consumption is stopped, symptoms regress....more »
    43. Amegakaryocytic thrombocytopenia
     A blood disorder involving a deficiency of blood platelets required for normal blood clotting. The disorder may be present at birth (congenital) or acquired (e.g. autoimmune disorders)....more »
    44. Amyloidosis AL
     A disease involving the abnormal deposit of amyloid fibrils in virtually any part of the body - the heart, liver, kidney and peripheral and autonomic nerves are most commonly affected. The abnormal amyloid fibrils are produced abnormal plasma cells in the...more »
    45. Antepartum Eclampsia
     Antepartum eclampsia is the development of seizures or coma in pregnant women suffering from high blood pressure. Antepartum means that it occurs before delivery. Eclampsia is a serious condition which requires urgent medical treatment. Eclampsia may be a...more »
    46. Anti-plasmin deficiency, congenital
     A very rare inherited blood disorder involving a deficiency of antiplasmin which results in excessive bleeding....more »
    47. Aortic dilatation- joint hypermobility- arterial tortuosity
     A rare syndrome characterized by the dilation of the aortic root, hyperextensible joints and varicose veins...more »
    48. Asthma
     Repeated attacks of breathing difficulty....more »
    49. Bartenwerfer syndrome
     A rare disorder characterized by dwarfism and facial and skeletal abnormalities. The disorder is a variant of Morquio disease....more »
    50. Bernard-Soulier Syndrome
     A rare inherited blood coagulation disorder caused by blood platelet abnormalities which results in easy bruising and excessive bleeding....more »
    51. Besnier-Boeck-Schaumann disease
     A rare disease where inflammatory granular nodules form in various organs....more »
    52. Biliary cirrhosis
     Biliary cirrhosis is a condition where the bile ducts are unable to transport bile effectively due to blockage, inflammation, scarring or some other damage to the bile ducts. The condition may result from such things as congenital defect of the bile ducts...more »
    53. Birt-Hogg-Dube syndrome
     A rare inherited disorder that affects the skin and results in an increased risk of certain skin tumors called fibrofolliculomas which are benign....more »
    54. Blood coagulation disorders, inherited
     Inherited blood disorders where the ability to form clots is dysfunctional. The blood needs to be able to clot to prevent excessive bleeding in situations such as when the body suffers some sort of injury. With blood coagulation disorders, the blood's abi...more »
    55. Bone-Marrow failure syndromes
     A disorder where the bone marrow fails to produce enough new blood cells....more »
    56. Bronchogenic carcinoma
     When cells of the lung start growing rapidly in an uncontrolled manner, the condition is called lung cancer ....more »
    57. CML-Like Syndrome, Familial
     A very rare condition characterized by symptom similar to myelocytic leukemia that develop during infancy. The condition can result in death during the first years of life....more »
    58. COPD
     Severe obstruction of bronchial air flow typically from bronchitis and/or emphysema....more »
    59. Carbohydrate deficiency glycoprotein syndrome type II
     Congenital disorders of glycosylation is a group of very rare inherited metabolic disorder where defective carbohydrate compounds are attached to glycoproteins and thus impairing glycoprotein function. Type 2 is caused by a genetic defect which involves t...more »
    60. Cartilage Hair Hypoplasia
     A rare genetic disorder characterized by short stature, skeletal abnormalities and fine, fragile hair....more »
    61. Cartilage-hair hypoplasia-like syndrome
     A rare syndrome characterized by thin hair shafts, short stature, short limbs and other skeletal abnormalities. The condition is identical to the skeletal abnormality component of cartilage-hair hypoplasia syndrome....more »
    62. Caterpillar complication poisoning
     The spines on certain caterpillars can cause a skin reaction as well as systemic symptoms if ingested. The nature of the symptoms vary depending on the species of caterpillar involved. Some only produce skin reactions whereas others can produce systemic s...more »
    63. Caterpillar-induced bleeding syndrome
     Caterpillars from the Lonomia genus have spines along their body which can penetrate human skin and cause blood coagulation problems. The severity of the symptoms vary depending on the degree of envenomation but serious cases can result in death....more »
    64. Caterpillar-induced bleeding syndrome -- Lonomia achelous
     Lonomia achelous caterpillars are native to Northern Brazil and Venezuela. They have spines along their body which can penetrate human skin and cause blood coagulation problems. The severity of the symptoms vary depending on the degree of envenomation but...more »
    65. Caterpillar-induced bleeding syndrome -- Lonomia obliqua
     Lonomia obliqua caterpillars are native to Southern Brazil and have spines along their body which can penetrate human skin and cause blood coagulation problems. The severity of the symptoms vary depending on the degree of envenomation but serious cases ca...more »
    66. Chediak-Higashi Syndrome
     An inherited immune system disorder characterized by reduced pigmentation, recurrent infection and neurological disorders....more »
    67. Chemical poisoning -- Anticoagulant rodenticide
     Anticoagulant rodenticide is a chemical used to control rodents. The type and severity of symptoms varies depending on the amount of chemical involved and the nature of the exposure....more »
    68. Chemical poisoning -- Brodifacoum
     Brodifacoum is a chemical used as a rodenticide. The chemical may be absorbed through the skin. Ingestion and other exposures to the chemical can cause various symptoms. The type and severity of symptoms varies depending on the amount of chemical involved...more »
    69. Chemical poisoning -- Bromadiolone
     Bromadiolone is a chemical used as a rodenticide. The chemical may be absorbed through the skin. Ingestion and other exposures to the chemical can cause various symptoms. The type and severity of symptoms varies depending on the amount of chemical involve...more »
    70. Child abuse
     Physical, sexual, emotional abuse or neglect of child....more »
    71. Chlorophacinone rodenticide poisoning
     Chlorophacinone is used as a rodenticide. The chemical may be absorbed through the skin. Ingestion and other exposures to the chemical can cause various symptoms. The type and severity of symptoms varies depending on the amount of chemical involved and th...more »
    72. 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 »
    73. Chromosome 3q29 microduplication syndrome
     A rare chromosomal disorder where a small portion of chromosome 3 is duplicated. The main features are mental retardation and some minor facial anomalies....more »
    74. Chromosome Xp11.23-p11.22 Duplication syndrome
     A rare syndrome characterized by the association of a large head, lack of hair, scoliosis and a skin anomaly. The reported patients tend to involve parents who were related....more »
    75. Chronic Idiopathic Myelofibrosis
     The bone marrow is consists of tissues which make blood cells and fibrous tissue supports these tissues that make the blood cells. In chronic idiopathic myelofibrosis, abnormal cells and fibres build up inside the bone marrow resulting in the production o...more »
    76. Chronic Lymphocytic Leukemia, Susceptibility to
     A cancer of the blood and bone marrow where too many abnormal lymphocytes (white blood cells) are produced which eventually crowds out healthy blood cells in the body. Researchers have discovered a link between a number of genetic defects and increased su...more »
    77. Chronic Lymphocytic Leukemia, Susceptibility to, 1
     A cancer of the blood and bone marrow where too many abnormal lymphocytes (white blood cells) are produced which eventually crowds out healthy blood cells in the body. Researchers have discovered a link between a number of genetic defects and increased su...more »
    78. Chronic Lymphocytic Leukemia, Susceptibility to, 2
     A cancer of the blood and bone marrow where too many abnormal lymphocytes (white blood cells) are produced which eventually crowds out healthy blood cells in the body. Researchers have discovered a link between a number of genetic defects and increased su...more »
    79. Chronic Lymphocytic Leukemia, Susceptibility to, 3
     A cancer of the blood and bone marrow where too many abnormal lymphocytes (white blood cells) are produced which eventually crowds out healthy blood cells in the body. Researchers have discovered a link between a number of genetic defects and increased su...more »
    80. Chronic Lymphocytic Leukemia, Susceptibility to, 4
     A cancer of the blood and bone marrow where too many abnormal lymphocytes (white blood cells) are produced which eventually crowds out healthy blood cells in the body. Researchers have discovered a link between a number of genetic defects and increased su...more »
    81. Chronic Lymphocytic Leukemia, Susceptibility to, 5
     A cancer of the blood and bone marrow where too many abnormal lymphocytes (white blood cells) are produced which eventually crowds out healthy blood cells in the body. Researchers have discovered a link between a number of genetic defects and increased su...more »
    82. Chronic Myeloproliferative Disorders
     A group of blood cancers where excessive numbers of blood cells are made by overactive or cancerous bone marrow. The number of excess blood cells tends to grow slowly. Examples of such disorders includes chronic myelogenous leukemia, polycythemia vera and...more »
    83. Chronic Neutrophilic Leukemia
     A rare form of leukemia characterized by excessive levels of mature neutrophils....more »
    84. Chronic lymphocytic leukemia
     A cancer of the blood and bone marrow where too many abnormal lymphocytes (white blood cells) are produced which eventually crowds out healthy blood cells in the body....more »
    85. Chronic myelogenous leukemia
     A slow-growing cancer of the white blood cells where the bone marrow makes too many white blood cells which eventually invade various parts of the body....more »
    86. Chronic myelomonocytic leukemia
     A rare form of malignant bone marrow cancer involving the proliferation of immature precursors of certain blood cells - myelocytes and monocytes. The proliferation is slower than in acute forms of the disease....more »
    87. Chronic renal insufficiency
     Chronic lack of function of the renal system. Kidneys....more »
    88. Cirrhosis, familial
     Liver cirrhosis that is inherited in a familial pattern. The liver scarring (cirrhosis) is not caused by any discernable disease process. The liver becomes progressively scarred and its function is impaired....more »
    89. Coagulopathy
     A disorder of the blood where it fails to clot normally....more »
    90. Coal worker's pneumoconiosis
     A lung disease caused by breathing in coal dust. The condition is generally associated with employees in the coal industry. Symptoms usually resolve when exposure to coal dust stops....more »
    91. Coffin-Lowry syndrome
     A rare genetic disorder characterized by down slanting space between eyelids, bulbous nose, soft hands and tapering fingers....more »
    92. Congenital amegakaryocytic thrombocytopenia
     A rare birth disorder involving a deficiency of blood platelets required for normal blood clotting....more »
    93. Congenital aplastic anemia
     A genetic disorder where the bone marrow does not produce enough blood cells. Fanconi's anemia is an example of congenital aplastic anemia....more »
    94. Coumachlor rodenticide poisoning
     Coumachlor is used as a rodenticide. The chemical may be absorbed through the skin. Ingestion and other exposures to the chemical can cause various symptoms. The type and severity of symptoms varies depending on the amount of chemical involved and the nat...more »
    95. Coumafuryl rodenticide poisoning
     Coumafuryl is used as a rodenticide. The chemical may be absorbed through the skin. Ingestion and other exposures to the chemical can cause various symptoms. The type and severity of symptoms varies depending on the amount of chemical involved and the nat...more »
    96. Coumatetralyl rodenticide poisoning
     Coumatetralyl is used as a rodenticide. The chemical may be absorbed through the skin. Ingestion and other exposures to the chemical can cause various symptoms. The type and severity of symptoms varies depending on the amount of chemical involved and the ...more »
    97. 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 »
    98. Cutis laxa, recessive type 2
     A very rare syndrome characterized primarily by loose skin and delayed development....more »
    99. 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 »
    100. DIC
     DIC s a syndrome triggered by a number of medical conditions including malignancy, infection and liver disease, and results in consumption of clotting factors in the blood....more »
    101. Deafness -- lymphoedema -- leukemia
     A rare syndrome characterized by deafness, early-onset leukemia and lymphoedema in the lower legs....more »
    102. Decompression sickness
     Condition from overly rapid decompression, especially when diving....more »
    103. Del(1) (q42-qter)
     A very rare chromosomal disorder where a portion of the long arm (q42-qter) of chromosome one is missing. The type and severity of symptoms is variable....more »
    104. Diabetes
     Failing or reduced ability of the body to handle sugars....more »
    105. Difenacoum rodenticide poisoning
     Difenacoum is used as a rodenticide. The chemical may be absorbed through the skin. Ingestion and other exposures to the chemical can cause various symptoms. The type and severity of symptoms varies depending on the amount of chemical involved and the nat...more »
    106. Difethialone rodenticide poisoning
     Difethialone is used as a rodenticide. The chemical may be absorbed through the skin. Ingestion and other exposures to the chemical can cause various symptoms. The type and severity of symptoms varies depending on the amount of chemical involved and the n...more »
    107. Diphacinone rodenticide poisoning
     Diphacinone is used as a rodenticide. The chemical may be absorbed through the skin. Ingestion and other exposures to the chemical can cause various symptoms. The type and severity of symptoms varies depending on the amount of chemical involved and the na...more »
    108. Dup (2) (pter-p23)
     A rare chromosomal disorder characterized by various anomalies. The listed symptoms are those observed in the few reported cases. The manifestations linked to most genetic defects are often variable to some degree....more »
    109. EDS V
     A rare genetic connective tissue disorder characterized by skin hyperextensibility, moderate joint hypermobility and moderate vascular fragility....more »
    110. Eclampsia
     Eclampsia is the development of seizures or coma in pregnant women suffering from high blood pressure. Eclampsia is a serious condition which requires urgent medical treatment. Eclampsia may be associated with moderate as well as significant increases in ...more »
    111. Ehlers Danlos syndrome type 4, autosomal dominant
     A rare genetic connective tissue disorder characterized by delicate skin, fragile blood vessels, distinctive facial features and minimal joint problems - previously known as EDS type 4....more »
    112. Ehlers-Danlos syndrome
     A group of inherited connective tissue disorders primarily involving the joints and skin. There are 11 disorders in the group....more »
    113. Ehlers-Danlos syndrome Type I
     A rare genetic connective tissue disorder characterized by hyperextensible joints, hyperextensible skin and poor wound healing....more »
    114. Ehlers-Danlos syndrome caused by tenascin-X deficiency
     A rare genetic disorder which is similar to Ehlers-Danlos syndrome and involves a deficiency of tenascin-X which affects connective tissue. The main symptoms are loose joints, partially dislocated joints and fragile, hyperextensible skin....more »
    115. Ehlers-Danlos syndrome type 4
     A rare genetic connective tissue disorder characterized by small joint hypermobility, easy bruising and characteristic facial appearance - a vascular or ecchymotic form of the condition....more »
    116. Ehlers-Danlos syndrome type II
     A rare genetic connective tissue disorder characterized by hypermobile joints, hyperextensible skin and poor wound healing - a milder form of Type 1 with hypermobility limited to hands and feet....more »
    117. Ehlers-Danlos syndrome type IV
     A rare genetic connective tissue disorder characterized by small joint hypermobility, easy bruising and characteristic facial appearance - a vascular or ecchymotic form of the condition....more »
    118. Ehlers-Danlos syndrome type V
     A rare genetic connective tissue disorder characterized by skin hyperextensibility, moderate joint hypermobility and moderate vascular fragility....more »
    119. Ehlers-Danlos syndrome type VI
     A rare genetic connective tissue disorder characterized by lax joints, scoliosis and fragile sclera of the eye - Ehlers Danlos type with predominant ocular abnormalities....more »
    120. Ehlers-Danlos syndrome with periventricular heterotopia
     The association of a brain malformation (periventricular nodular heterotopia) with a connective tissue disorder called Ehlers-Danlos syndrome....more »
    121. Ehlers-Danlos syndrome, 6B
     A rare genetic connective tissue disorder characterized by lax joints, scoliosis and fragile sclera of the eye - Ehlers Danlos type with predominant ocular abnormalities but lysyl-hydroxylase activity is normal1....more »
    122. Ehlers-Danlos syndrome, arthrochalasic type
     A rare genetic connective tissue disorder characterized by hyperextensible and fragile skin and hypermobile joints which leads to dislocations, osteoarthritis and fractures - previously known as EDS types 7A and 7B....more »
    123. Ehlers-Danlos syndrome, cardiac valvular form
     A rare genetic connective tissue disorder characterized by hypermobile joints, joint dislocations and skin hyperextensibility and fragility....more »
    124. Ehlers-Danlos syndrome, classic type
     A rare genetic connective tissue disorder characterized by hypermobile joints, joint dislocations and skin hyperextensibility and fragility - a combination of ED types I and II....more »
    125. Ehlers-Danlos syndrome, dermatosparaxis type
     A rare genetic connective tissue disorder characterized by skin hyperextensibility hypermobile joints and fragile skin which loses its elasticity - previously known as EDS type 7C....more »
    126. Ehlers-Danlos syndrome, dermatospraxis type
     A rare genetic connective tissue disorder characterized by skin hyperextensibility hypermobile joints and fragile skin which loses its elasticity - previously known as EDS type 7C....more »
    127. Ehlers-Danlos syndrome, hypermobility type
     A rare genetic connective tissue disorder characterized by hypermobile joints, hyperextensible skin and - previously known as EDS type 3....more »
    128. Ehlers-Danlos syndrome, kyphoscoliosis type
     A rare genetic connective tissue disorder caused by deficiency of the lysyl hydroxylase enzyme and is characterized by progressive scoliosis and muscle weakness and fragile sclera - previously known as EDS type 6....more »
    129. Ehlers-Danlos syndrome, progeroid form 2
     A rare genetic connective tissue disorder characterized by hypermobile joints, fragile skin, mental retardation and short stature....more »
    130. Ehlers-Danlos syndrome, tenascin-X deficiency
     A rare genetic connective tissue disorder characterized by hypermobile joints, joint dislocations and skin hyperextensibility and fragility....more »
    131. Ehlers-Danlos syndrome, vascular type
     A rare genetic connective tissue disorder characterized by delicate skin, fragile blood vessels, distinctive facial features and minimal joint problems - previously known as EDS type 4....more »
    132. Emanuel syndrome
     A rare chromosomal disorder where a portion of chromosome 11 is translocated with a portion of chromosome 22. The disorder involves a wide range of abnormalities such as kidney, genital and heart abnormalities, mental retardation, small head and failure t...more »
    133. Emphysema
     Emphysema is a type of chronic obstructive pulmonary disease (COPD). It is defined as an abnormal, permanent enlargement of the air spaces distal to the terminal bronchioles accompanied by destruction of their walls and without obvious fibrosis....more »
    134. Endometriosis
     Misplaced uterus tissue causing scar tissue....more »
    135. Epidermolysis bullosa simplex, Ogna type
     An inherited skin blistering condition characterized by blisters on palms and soles....more »
    136. Essential thrombocytopenia
     A rare blood disorder characterized by an excessively low number of platelets in the blood which often results in hemorrhages....more »
    137. 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 »
    138. 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 »
    139. 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 »
    140. 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 »
    141. 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 »
    142. 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 »
    143. 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 »
    144. 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 »
    145. 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 »
    146. 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 »
    147. 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 »
    148. 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 »
    149. 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 »
    150. 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 »
    151. 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 »
    152. 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 »
    153. 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 »
    154. 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 »
    155. 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 »
    156. 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 »
    157. 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 »
    158. Familial platelet syndrome with predisposition to acute myelogenous leukemia
     A rare inherited blood disorder that is associated with an increased risk of myeloid malignancies - especially acute myelogenous leukemia....more »
    159. Fanconi's anemia
     Fanconi's anemia is a rare inherited blood disorder characterized by the inability of the bone marrow to produce blood cells. An increased incidence of leukemias and other cancers is associated with this condition and various skeletal abnormalities and ot...more »
    160. Fanconi's anemia -- Complementation group A
     Fanconi's anemia is a rare inherited blood disorder characterized by the inability of the bone marrow to produce blood cells. The subtype called Complementation group A refers to a genetic subtype of the disease. An increased incidence of leukemias and ot...more »
    161. Fanconi's anemia -- Complementation group B
     Fanconi's anemia is a rare inherited blood disorder characterized by the inability of the bone marrow to produce blood cells. The subtype called Complementation group B refers to a genetic subtype of the disease. An increased incidence of leukemias and ot...more »
    162. Fanconi's anemia -- Complementation group C
     Fanconi's anemia is a rare inherited blood disorder characterized by the inability of the bone marrow to produce blood cells. The subtype called Complementation group C refers to a genetic subtype of the disease. An increased incidence of leukemias and ot...more »
    163. Fanconi's anemia -- Complementation group D1
     Fanconi's anemia is a rare inherited blood disorder characterized by the inability of the bone marrow to produce blood cells. The subtype called Complementation group D1 refers to a genetic subtype of the disease. An increased incidence of leukemias and o...more »
    164. Fanconi's anemia -- Complementation group D2
     Fanconi's anemia is a rare inherited blood disorder characterized by the inability of the bone marrow to produce blood cells. The subtype called Complementation group D2 refers to a genetic subtype of the disease. An increased incidence of leukemias and o...more »
    165. Fanconi's anemia -- Complementation group E
     Fanconi's anemia is a rare inherited blood disorder characterized by the inability of the bone marrow to produce blood cells. The subtype called Complementation group E refers to a genetic subtype of the disease. An increased incidence of leukemias and ot...more »
    166. Fanconi's anemia -- Complementation group F
     Fanconi's anemia is a rare inherited blood disorder characterized by the inability of the bone marrow to produce blood cells. The subtype called Complementation group F refers to a genetic subtype of the disease. An increased incidence of leukemias and ot...more »
    167. Fanconi's anemia -- Complementation group G
     Fanconi's anemia is a rare inherited blood disorder characterized by the inability of the bone marrow to produce blood cells. The subtype called Complementation group G refers to a genetic subtype of the disease. An increased incidence of leukemias and ot...more »
    168. Fanconi's anemia -- Complementation group I
     Fanconi's anemia is a rare inherited blood disorder characterized by the inability of the bone marrow to produce blood cells. The subtype called Complementation group I refers to a genetic subtype of the disease. An increased incidence of leukemias and ot...more »
    169. Fanconi's anemia -- Complementation group J
     Fanconi's anemia is a rare inherited blood disorder characterized by the inability of the bone marrow to produce blood cells. The subtype called Complementation group J refers to a genetic subtype of the disease. An increased incidence of leukemias and ot...more »
    170. Fanconi's anemia -- Complementation group L
     Fanconi's anemia is a rare inherited blood disorder characterized by the inability of the bone marrow to produce blood cells. The subtype called Complementation group L refers to a genetic subtype of the disease. An increased incidence of leukemias and ot...more »
    171. Fanconi's anemia -- Complementation group M
     Fanconi's anemia is a rare inherited blood disorder characterized by the inability of the bone marrow to produce blood cells. The subtype called Complementation group M refers to a genetic subtype of the disease. An increased incidence of leukemias and ot...more »
    172. Fanconi's anemia -- Complementation group N
     Fanconi's anemia is a rare inherited blood disorder characterized by the inability of the bone marrow to produce blood cells. The subtype called Complementation group N refers to a genetic subtype of the disease. An increased incidence of leukemias and ot...more »
    173. Fanconi's anemia -- Estren-Dameshek variant
     Fanconi's anemia is a rare inherited blood disorder characterized by the inability of the bone marrow to produce blood cells. The Estren-Dameshek variant is Fanconi's anemia without the presence of any physical malformations or deformities which are often...more »
    174. Fanconi's syndrome
    175. Finale rodenticide poisoning
     Finale is used as a rodenticide. The chemical may be absorbed through the skin. Ingestion and other exposures to the chemical can cause various symptoms. The type and severity of symptoms varies depending on the amount of chemical involved and the nature ...more »
    176. Flail Chest
     The separation of a portion of the rib cage from the rest of the chest wall - usually due to trauma. The severity of the condition varies depending on the extent of the damage....more »
    177. Flocoumafen rodenticide poisoning
     Flocoumafen is used as a rodenticide. The chemical may be absorbed through the skin. Ingestion and other exposures to the chemical can cause various symptoms. The type and severity of symptoms varies depending on the amount of chemical involved and the na...more »
    178. Folgorat rodenticide poisoning
     Folgorat is used as a rodenticide. The chemical may be absorbed through the skin. Ingestion and other exposures to the chemical can cause various symptoms. The type and severity of symptoms varies depending on the amount of chemical involved and the natur...more »
    179. Fragile-X Syndrome
     A rare inherited characterized by various physical anomalies as well as mental retardation. The symptoms are milder in females....more »
    180. Gaucher Disease
     A rare inherited biochemical disorder characterized by the deficiency of the enzyme called glucocerebrosidase and accumulation of glycosylceramide (glucocerebroside). There are three forms of this disease: type 1, 2 and 3....more »
    181. Gaucher disease type 1
     A rare inherited biochemical disorder characterized by the deficiency of the enzyme called glucocerebrosidase and accumulation of glycosylceramide (glucocerebroside). There are three forms of this disease: type 1, 2 and 3. Type 1 is the visceral, chronic ...more »
    182. Gaucher disease type 2
     A rare inherited biochemical disorder characterized by the deficiency of the enzyme called glucocerebrosidase and accumulation of glycosylceramide (glucocerebroside). There are three forms of this disease: type 1, 2 and 3. Type 2 is acute neurological for...more »
    183. Gaucher disease type 3
     A rare inherited biochemical disorder characterized by the deficiency of the enzyme called glucocerebrosidase and accumulation of glycosylceramide (glucocerebroside). There are three forms of this disease: type 1, 2 and 3. Type 3 is a subacute neurologica...more »
    184. Glycogen Storage Disease Type I
     An inherited metabolic disorder where a deficiency of the enzyme glucose-6-phosphatase prevents glycogen being turned into glucose leading to a buildup of glycogen in the liver and kidneys. Most problems tend to develop during adulthood....more »
    185. Glycogen storage disease type 1C
     A genetic metabolic disorder involving a deficiency of the enzyme glucose-6-phosphatase (due to a defect in the microsomal phosphate) which results in the accumulation of glycogen in various tissues. G6P is stored as glycogen until the body needs to conve...more »
    186. Glycogen storage disease type 1D
     A genetic metabolic disorder involving a deficiency of the enzyme glucose-6-phosphatase (due to a defect in the microsomal glucose transporter) which results in the accumulation of glycogen in various tissues. G6P is stored as glycogen until the body need...more »
    187. 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 »
    188. Haim-Munk syndrome
     A rare inherited disorder involving red, thickened patches of skin on the palms and soles, skin infections and nail and teeth abnormalities....more »
    189. Hairy cell leukemia
     A chronic leukemia which causes an excess of abnormal mononuclear cells which appear hair like under microscopy...more »
    190. Havoc rodenticide poisoning
     Havoc is used as a rodenticide. The chemical may be absorbed through the skin. Ingestion and other exposures to the chemical can cause various symptoms. The type and severity of symptoms varies depending on the amount of chemical involved and the nature o...more »
    191. Hemophagocytic lymphohistiocytosis, familial, 1
     A rare recessively inherited disorder involving an overactive immune system. More specifically, the body becomes infiltrated by large numbers of histiocytes (macrophages) that accumulate in various organs such as the liver, spleen, bone marrow, skin and c...more »
    192. Hemophagocytic lymphohistiocytosis, familial, 2
     A rare recessively inherited disorder involving an overactive immune system. More specifically, the body becomes infiltrated by large numbers of histiocytes (macrophages) that accumulate in various organs such as the liver, spleen, bone marrow, skin and c...more »
    193. Hemophagocytic lymphohistiocytosis, familial, 3
     A rare recessively inherited disorder involving an overactive immune system. More specifically, the body becomes infiltrated by large numbers of histiocytes (macrophages) that accumulate in various organs such as the liver, spleen, bone marrow, skin and c...more »
    194. Hemophagocytic lymphohistiocytosis, familial, 4
     A rare recessively inherited disorder involving an overactive immune system. More specifically, the body becomes infiltrated by large numbers of histiocytes (macrophages) that accumulate in various organs such as the liver, spleen, bone marrow, skin and c...more »
    195. Hemophilia A
     A rare coagulation disorder caused by a deficiency of factor VIII which results in bleeding problems....more »
    196. Hemophilia B
     A rare coagulation disorder caused by a deficiency of factor IX which results in bleeding problems....more »
    197. Hereditary macrothrombocytopenia
     A rare inherited blood disorder where the blood platelets are abnormally large. Blood platelets are involved in the blood clotting process but patients with the condition often have no symptoms or suffer mild bleeding problems....more »
    198. Hermansky-Pudlak Syndrome
     A rare disorder characterized by various degrees of albinism, bleeding due to a platelet defect and accumulation of a waxy substance in cells (lysosomal ceroid storage)....more »
    199. Hermansky-Pudlak syndrome type 2
     A rare disorder characterized by various degrees of albinism, bleeding due to a platelet defect, an accumulation of a waxy substance in cells (lysosomal ceroid storage) and immunodeficiency. HPS type 2 differs from type 1 in that it also involves immunode...more »
    200. Human T-lymphotropic virus type 3
     A former name used for HIV which is an infectious viral disease. The infection usually has an initial symptom-free period which is followed by various stages of increasing severity....more »
    201. Hypersplenism
     A condition which is characterized by the exaggeration of blood degrading function of the spleen...more »
    202. Ichthyosis-cheek-eyebrow syndrome
     A rare genetic disorder involving sparse eyebrows, full cheeks and a skin condition characterized by fish-like scales....more »
    203. Immune thrombocytopenia
     A rare disorder where the body's immune system attacks blood platelets which affect the blood's ability to clot....more »
    204. Indandione rodenticide poisoning
     Indandione is used as a rodenticide. The chemical may be absorbed through the skin. Ingestion and other exposures to the chemical can cause various symptoms. The type and severity of symptoms varies depending on the amount of chemical involved and the nat...more »
    205. Infantile apnea
     A disorder where infants stop breathing temporarily....more »
    206. Injury
     Any damage inflicted in the body...more »
    207. Isotretinoin -- Teratogenic Agent
     There is evidence to indicate that exposure to Isotretinoin (an acne treatment drug) 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 affect...more »
    208. Keratosis palmoplantaris -- periodontopathia -- onychogryposis
     A rare syndrome characterized by gum disease, nail and skin problems and various other anomalies....more »
    209. Kidney failure
     Total failure of the kidneys to filter waste...more »
    210. Klerat rodenticide poisoning
     Klerat is used as a rodenticide. The chemical may be absorbed through the skin. Ingestion and other exposures to the chemical can cause various symptoms. The type and severity of symptoms varies depending on the amount of chemical involved and the nature ...more »
    211. Langerhans Cell Histiocytosis
     A condition which is characterized by proliferation of Langerhans cells...more »
    212. Leukemia, Lymphocytic, Acute, L1
     Acute lymphocytic leukemia is a cancer of the white blood cells. Precursors to white blood cells are called blasts and are made by the bone marrow but in ALL the blasts are abnormal and do not develop into lymphocytes. Instead, the abnormal blasts or leuk...more »
    213. Leukemia, Lymphocytic, Acute, L2
     Acute lymphocytic leukemia is a cancer of the white blood cells. Precursors to white blood cells are called blasts and are made by the bone marrow but in ALL the blasts are abnormal and do not develop into lymphocytes. Instead, the abnormal blasts or leuk...more »
    214. Leukemia, Lymphocytic, Acute, L3
     Acute lymphocytic leukemia is a relatively aggressive cancer of the white blood cells. Precursors to white blood cells are called blasts and are made by the bone marrow but in ALL the blasts are abnormal and do not develop into lymphocytes. Instead, the a...more »
    215. 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 »
    216. 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 »
    217. Leukemia, Myeloid, Chronic
     A slow-growing 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....more »
    218. Leukemia, Myeloid, Philadelphia-Negative
     Acute lymphocytic leukemia is a relatively aggressive cancer of the white blood cells. Precursors to white blood cells are called blasts and are made by the bone marrow but in ALL the blasts are abnormal and do not develop into lymphocytes. Instead, the a...more »
    219. Leukemia, Myeloid, Philadelphia-Positive
     A relatively aggressive cancer of the cells that produce white blood cells. The Philadelphia form of myeloid leukemia carries a relatively poor prognosis. It involves an acquired genetic mutation which results in the production tyrosine kinase which cause...more »
    220. Leukemia, T-cell, chronic
     Cancer of blood cells called T-cells which form part of the immune system....more »
    221. Liver conditions
     Any condition that affects the liver...more »
    222. Loeys-Dietz syndrome
     A very rare syndrome characterized mainly by a bulge in the aorta (aneurysm), wide set eyes, cleft palate, divided uvula and twisted arteries....more »
    223. Lung abscess
     Pus (abscess) in the lung...more »
    224. Lupus
     Autoimmune disease with numerous effects on various organs and linings....more »
    225. Lymphangioleiomyomatosis
     A very rare progressive disease where an unusual type of muscle cell (smooth muscle) infiltrates the lungs which eventually obstructs the flow of air through the lungs. The cause is unknown and generally occurs in women of child bearing age....more »
    226. Lymphoblastic lymphoma
     A cancer of the lymph system which usually involves immature T-lymphocytes and sometimes B-lymphocytes. The cancer usually affects the mediastinum (between the lungs), bone marrow, brain and spinal cord....more »
    227. Lymphocytic leukemia
     A condition characterized by the proliferation of lymphoid tissues...more »
    228. MPS-IV (Morquio Disease)
     A condition which is characterized by biochemically distinct mucopolysaccharidosis...more »
    229. Marchiafava-Micheli disease
     A blood disorder where abnormalities in erhtyrocyte membranes results in excessive destruction of red blood cells and hence anemia....more »
    230. Marfan syndrome
     A genetic connective tissue disorder involving a defect of chromosome 15q21.1 which affects the production of the fibrillin needed to make connective tissue....more »
    231. Marfan-Like syndrome
     Any congenital condition with a group of symptoms that resembles Marfan syndrome but doesn't quite fulfill all the criteria. Marfan syndrome is a connective tissue disorder that affects the skeleton, lungs, eyes, heart and blood vessels....more »
    232. Matikus rodenticide poisoning
     Matikus is used as a rodenticide. The chemical may be absorbed through the skin. Ingestion and other exposures to the chemical can cause various symptoms. The type and severity of symptoms varies depending on the amount of chemical involved and the nature...more »
    233. 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 »
    234. 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 »
    235. Meconium aspiration syndrome
     A condition that occurs when an infant suffers respiratory distress following birth due to the presence of meconium in the amniotic fluid....more »
    236. Mental retardation, X-linked, 45
     A rare form of mental retardation inherited in a X-linked manner. It occurs as a result of a defect in the zinc finger protein-81 gene on chromosome Xp22.1-p11....more »
    237. Mental retardation, X-linked, Siderius type
     A rare inherited form of mental retardation involving a defect on chromosome Xp11.2....more »
    238. Morquio syndrome, type B
     A rare inherited biochemical disorder characterized by the accumulation of mucopolysaccharides (glycosaminoglycans) in various body tissues due to insufficient amounts of the enzyme (? galactosidase) needed to break it down....more »
    239. Mouser rodenticide poisoning
     Mouser is used as a rodenticide. The chemical may be absorbed through the skin. Ingestion and other exposures to the chemical can cause various symptoms. The type and severity of symptoms varies depending on the amount of chemical involved and the nature ...more »
    240. Mucopolysaccharidosis IV
     Disorder of mucopolysaccharide metabolism in infants....more »
    241. Multiple Myeloma
     A rare malignant cancer that occurs in the bone marrow. More common in skull, spine, rib cage, pelvis and legs....more »
    242. Myelodysplastic/myeloproliferative disease
     A rare group of blood and bone marrow diseases which contains features of myelodysplastic and myeloproliferative disease. Myelodysplastic disease is when the immature blood cells do not develop into normal functioning mature cells. Myeloproliferative dise...more »
    243. Myelofibrosis-osteosclerosis
     Formation of fibrous tissue in the bone marrow in response to bone marrow damage....more »
    244. Myelogenous leukemia
     A condition which is characterized proliferation of myeloid tissue and the abnormal increase in granulocytes...more »
    245. Myeloproliferative diseases
     Myeloproliferative diseases are a diverse group of diseases characterised by proliferation of cells in one or more blood cell lines, but is distinct from leukemia. Diseases include chronic myelogenous leukemia, polycythemia rubra vera, myelofibrosis and e...more »
    246. Myelpathic anemia
     Myelopathic anemia is a form of anemia resulting from the development of abnormal tissue in the bone marrow - usually metastatic cancers. It is characterized by abnormal number of immature blood cells in the blood....more »
    247. NASH syndrome
     A form of fatty liver where fat and fibrous tissue accumulate in the liver. Fatty liver is normally seen in alcoholic patients but in NASH syndrome, alcohol is not a factor. The condition may be generally asymptomatic or in some cases may lead to progress...more »
    248. Niemann-Pick disease
     A rare inherited biochemical disorder involving the deficiency of an enzyme (acid sphingomyelinase) needed to break down certain lipids which results in an accumulation of these lipids in the body....more »
    249. Nonkeratan-sulfate-excreting Morquio syndrome
     A rare inherited biochemical disorder characterized by the accumulation of mucopolysaccharides (glycosaminoglycans) in various body tissues due to insufficient amounts of certain enzymes needed to break it down. This disorder is distinguished form other s...more »
    250. OFD syndrome type 8
     A rare genetic disorder characterized by oral frenula, oral clefts, underdeveloped nose flaps and finger abnormalities....more »
    251. OI, Type I
     A genetic condition characterized mainly by fragile bones that fracture easily and blue sclerae. The fractures tend start during early childhood (when walking starts) and becomes worse after menopause or in old age. Fractures tend to heal normally. Type I...more »
    252. Occupational Cancer -- Hematopoietic system cancer
     Occupational exposure to X-radiation can increase the risk of developing hematopoietic system cancer....more »
    253. Occupational Cancer -- Mesothelioma
     Occupational exposure to asbestos can increase the risk of developing mesothelioma....more »
    254. Osteogenesis imperfecta Type I
     A rare genetic connective tissue disorder characterized by fragile bones, blue sclerae and hyperextensible joints....more »
    255. Osteogenesis imperfecta type IV
     A rare genetic connective tissue disorder characterized by fragile bones and blue sclerae. The osteoporosis tends to be moderate and there is generally no joint hyperextensibility....more »
    256. Osteogenesis imperfecta, type 1A
     A rare genetic connective tissue disorder characterized by fragile bones and hyperextensible joints - a type of osteogenesis imperfecta I where the teeth are opalescent and blue sclerae may be absent....more »
    257. Osteogenesis imperfecta, type 1B
     A rare genetic connective tissue disorder characterized by fragile bones and hyperextensible joints - a milder form of osteogenesis imperfecta I where the teeth are normal and blue sclerae may be absent....more »
    258. Osteogenesis imperfecta, type 4
     A rare genetic connective tissue disorder characterized by fragile bones and blue sclerae - a form of OI involving moderate osteoporosis and no joint hyperextensibility....more »
    259. 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 »
    260. Phenylbutazone -- Teratogenic Agent
     There is evidence to indicate that exposure to Phenylbutazone 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 »
    261. Philadelphia-negative chronic myeloid leukemia
     A form of leukemia....more »
    262. Pindone rodenticide poisoning
     Pindone is used as a rodenticide. The chemical may be absorbed through the skin. Ingestion and other exposures to the chemical can cause various symptoms. The type and severity of symptoms varies depending on the amount of chemical involved and the nature...more »
    263. Pleuropulmonary blastoma
     A type of tumor that originates from precursor cells or blasts (immature or embryonic tissue) in the lungs or covering of the lungs....more »
    264. Pneumonia
     Infection of the lung by bacteria, viruses or fungus....more »
    265. Polycythemia vera
     A condition which is characterized by myeloproliferation of unknown etiology...more »
    266. Posterior tibial tendon rupture
     Rupture of the tendon at the bottom of the foot that helps maintain the foot arch. Some people are more prone to this condition than others - e.g. those who are over weight or have a history of flat feet. The pain usually begins on the inside of the foot ...more »
    267. Prothrombin deficiency
     A rare disorder involving a deficiency of a protein (prothrombin or factor II) involved in blood clotting. The severity of symptoms vary according to the level of deficiency....more »
    268. Pseudoxanthoma elasticum
     A group of inherited, progressive connective tissue disorders affecting the skin, eyes and cardiovascular system. The condition is characterized by calcium deposits in the connective tissue which affects its ability to function. Some cases remain undiagno...more »
    269. Pulmonary edema
     Severe condition of excess fluid in the lungs....more »
    270. Pulmonary embolism
     Blocked lung blood vessel often from a blood clot....more »
    271. Rasmussen-Johnsen-Thomsen syndrome
     A very rare syndrome characterized mainly by the lack of an ear canal opening as well as foot deformities....more »
    272. Ratak Plus rodenticide poisoning
     Ratak Plus is used as a rodenticide. The chemical may be absorbed through the skin. Ingestion and other exposures to the chemical can cause various symptoms. The type and severity of symptoms varies depending on the amount of chemical involved and the nat...more »
    273. Raynaud's phenomenon
     Blood vessel constriction attacks affecting fingers and/or toes....more »
    274. Renal agenesis, bilateral
     A rare congenital malformation where the kidneys don't develop during the fetal stage resulting in insufficient amniotic fluid....more »
    275. Respiratory infections
     Any infection that occurs to the respiratory system...more »
    276. Respiratory-Bronchiolitis-associated Interstitial Lung Disease
     A relatively uncommon form of lung inflammation that has no apparent cause though the majority of patients have a history of smoking. Symptoms tend to develop over a period of six months to one and a half years....more »
    277. Retinopathy -- aplastic anemia -- neurological abnormalities
     A very rare syndrome characterized by retinal disease, aplastic anemia and neurological problems....more »
    278. Rib fracture
     A fracture of the ribs...more »
    279. Rodend rodenticide poisoning
     Rodend is used as a rodenticide. The chemical may be absorbed through the skin. Ingestion and other exposures to the chemical can cause various symptoms. The type and severity of symptoms varies depending on the amount of chemical involved and the nature ...more »
    280. Rubinstein-Taybi Syndrome
     A rare congenital disorder characterized by very small stature, broad thumbs and toes, slanted palpebral fissures and hypoplastic maxilla....more »
    281. 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 »
    282. 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 »
    283. Scleroderma
     A rare, progressive connective tissue disorder involving thickening and hardening of the skin and connective tissue. There are a number of forms of scleroderma with some forms being systemic (involving internal organs)....more »
    284. Secondary Biliary Cirrhosis
     Secondary biliary cirrhosis is a condition where the bile ducts are unable to transport bile effectively due to a secondary cause which results in blockage, inflammation, scarring or some other damage to the bile ducts. The condition may result from such ...more »
    285. Shock
     Severe condition from reduced blood circulation...more »
    286. Siderius type X-linked mental retardation syndrome
     A rare inherited form of mental retardation involving a defect on chromosome Xp11.2. The symptoms are evident in males but females may be carriers....more »
    287. Sphingolipidosis
     A group of diseases involving the abnormal metabolism and storage of a substance called sphingolipid. Symptoms will vary depending on the disease. Examples of diseases from this group include gangliosidosis, Gaucher's disease and Niemann-Pick disease....more »
    288. Spondylocarpotarsal synostosis
     A rare genetic disorder characterized by short stature, fusion of toe and finger bones and failure of spinal segmentation....more »
    289. Spondylometaphyseal dysplasia with combined immunodeficiency
     A rare syndrome characterized by skeletal abnormalities as well as a poor immune system....more »
    290. Storage pool platelet disease
     A rare disorder where blood platelet defects cause bleeding problems as the platelets are unable to function normally in the blood clotting process....more »
    291. 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 »
    292. 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 »
    293. T-cell acute lymphoblastic leukemia
     Cancer of particular white blood cells called T-cells. Precursors to white blood cells are called blasts and are made by the bone marrow but in ALL the blasts are abnormal and do not develop into lymphocytes. Instead, the abnormal blasts or leukemic cells...more »
    294. Talon rodenticide poisoning
     Talon is used as a rodenticide. The chemical may be absorbed through the skin. Ingestion and other exposures to the chemical can cause various symptoms. The type and severity of symptoms varies depending on the amount of chemical involved and the nature o...more »
    295. Thiopurine S methyltranferase deficiency
     A rare enzyme deficiency which is generally asymptomatic but can cause problems when certain anti-cancer or immunosuppressant drugs are used (e.g. 6-mercaptopurine, 6-thioguanine, azathioprine). The body is unable to metabolize these drugs which leads to ...more »
    296. Thrombasthenia
     An inherited blood clotting disorder where abnormal blood platelet function causes results in excessive bleeding....more »
    297. Thrombocytopathy
     A blood disorder where abnormal blood platelets affect blood coagulation....more »
    298. Thrombocytopenia -- cerebellar hypoplasia -- short stature
     A very rare syndrome characterized mainly by short stature, low blood platelets and abnormal brain development....more »
    299. Tuberculosis
     Bacterial infection causing nodules forming, most commonly in the lung....more »
    300. Type I Glycogen Storage Disease
     A condition which is characterized by a disease affecting glycogen storage...more »
    301. Urogenital adysplasia, hereditary
     A condition which is characterised by bilateral renal agenesis...more »
    302. Volak rodenticide poisoning
     Volak is used as a rodenticide. The chemical may be absorbed through the skin. Ingestion and other exposures to the chemical can cause various symptoms. The type and severity of symptoms varies depending on the amount of chemical involved and the nature o...more »
    303. Volid rodenticide poisoning
     Volid is used as a rodenticide. The chemical may be absorbed through the skin. Ingestion and other exposures to the chemical can cause various symptoms. The type and severity of symptoms varies depending on the amount of chemical involved and the nature o...more »
    304. Von Gierke Disease
     An inherited metabolic disorder where a deficiency of the enzyme glucose-6-phosphatase prevents glycogen being turned into glucose leading to a buildup of glycogen in the liver and kidneys....more »
    305. 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 »
    306. Waldenstrom macroglobulinemia
     A rare disorder involving malignancy of the lymph and blood cells....more »
    307. Whooping Cough
     An infectious condition caused by the bacteria Bordetella pertussis...more »
    308. Wiskott-Aldrich Syndrome
     An inherited immune system disorder that affects only males and is characterized by recurring infections, eczema and reduced level of blood platelets (thrombocytopenia)....more »
    309. X-linked dyserythropoietic anaemia and thrombocytopenia
     An inherited blood disorder characterized by dyserythropeoietic anemia (abnormal red blood cell formation) and low blood platelet count which can cause bleeding problems....more »
    310. X-linked mental retardation -- hypotonia
     A very rare inherited disorder characterized primarily by mental retardation. Initial symptoms of muscle weakness gives way to spasticity and contractures....more »
    311. Xylosylprotein 4-beta-galactosyltransferase (XGPT) deficiency
     A variant of the connective tissue disorder called Ehlers-Danlos. It is caused by a deficiency of galactosyltransferase I....more »

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