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Symptom Checker » Easy bruising » Low white blood cell count
 

Easy bruising and Low white blood cell count
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Results: Causes of Easy bruising AND Low white blood cell count

Results: 253 causes of Easy bruising OR Low white blood cell count

    1. ADP platelet receptor P2Y12, deficiency of
     Deficiency of a compound (P2Y12) involved in the blood clotting process which results in bleeding problems....more »
    2. 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 »
    3. ATRUS syndrome
     A rare syndrome characterized by fusion of the forearm bones near the elbow and a blood disorder....more »
    4. 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 »
    5. 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 »
    6. 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 »
    7. 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 »
    8. 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 »
    9. 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 »
    10. 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 »
    11. Acute biphenotypic leukemia
     A rare form of leukemia that has myeloid and lymphoid features....more »
    12. 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 »
    13. 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 »
    14. Acute leukemia
     An acute condition which affects a cell line of the blood which shows little or no differentiation...more »
    15. 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 »
    16. 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 »
    17. 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 »
    18. 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 »
    19. 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 »
    20. 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 »
    21. Acute myeloblastic leukemia type 1
     A form of blood cancer resulting in the rapid proliferation of immature blood cells (blast cells)....more »
    22. Acute myeloblastic leukemia type 2
     A form of blood cancer resulting in the rapid proliferation of granulocytes and monocytes....more »
    23. 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 »
    24. 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 »
    25. 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 »
    26. 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 »
    27. 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 »
    28. 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 »
    29. 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 »
    30. 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 »
    31. 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 »
    32. 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 »
    33. Acute myeloid leukemia, adult
     A form of blood cancer resulting in the rapid proliferation of granulocytes and monocytes, red blood cells and platelets....more »
    34. 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 »
    35. Aging
     The medical conditions from getting older....more »
    36. 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 »
    37. 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 »
    38. 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 »
    39. 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 »
    40. Anti-plasmin deficiency, congenital
     A very rare inherited blood disorder involving a deficiency of antiplasmin which results in excessive bleeding....more »
    41. Aortic dilatation- joint hypermobility- arterial tortuosity
     A rare syndrome characterized by the dilation of the aortic root, hyperextensible joints and varicose veins...more »
    42. Bernard-Soulier Syndrome
     A rare inherited blood coagulation disorder caused by blood platelet abnormalities which results in easy bruising and excessive bleeding....more »
    43. 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 »
    44. 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 »
    45. Bone-Marrow failure syndromes
     A disorder where the bone marrow fails to produce enough new blood cells....more »
    46. 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 »
    47. Carbenicillin -- Teratogenic Agent
     There is strong evidence to indicate that exposure to Carbenicillin 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 o...more »
    48. 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 »
    49. 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 »
    50. 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 »
    51. 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 »
    52. Chediak-Higashi Syndrome
     An inherited immune system disorder characterized by reduced pigmentation, recurrent infection and neurological disorders....more »
    53. 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 »
    54. 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 »
    55. 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 »
    56. Child abuse
     Physical, sexual, emotional abuse or neglect of child....more »
    57. 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 »
    58. 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 »
    59. 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 »
    60. 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 »
    61. 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 »
    62. 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 »
    63. 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 »
    64. 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 »
    65. 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 »
    66. Chronic Neutrophilic Leukemia
     A rare form of leukemia characterized by excessive levels of mature neutrophils....more »
    67. 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 »
    68. 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 »
    69. 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 »
    70. Chronic renal insufficiency
     Chronic lack of function of the renal system. Kidneys....more »
    71. 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 »
    72. Cloxapen -- Teratogenic Agent
     There is evidence to indicate that exposure to Cloxapen (an antibiotic) 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 lev...more »
    73. Coagulopathy
     A disorder of the blood where it fails to clot normally....more »
    74. Congenital amegakaryocytic thrombocytopenia
     A rare birth disorder involving a deficiency of blood platelets required for normal blood clotting....more »
    75. 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 »
    76. 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 »
    77. 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 »
    78. 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 »
    79. 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 »
    80. Cutler Syndrome
     A rare disorder characterized by multisystem disorders including muscle wasting, ataxia, epilepsy, anemia and kidney disease. The kidney disease is most likely present at birth....more »
    81. 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 »
    82. Deafness -- lymphoedema -- leukemia
     A rare syndrome characterized by deafness, early-onset leukemia and lymphoedema in the lower legs....more »
    83. 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 »
    84. 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 »
    85. 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 »
    86. EDS V
     A rare genetic connective tissue disorder characterized by skin hyperextensibility, moderate joint hypermobility and moderate vascular fragility....more »
    87. 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 »
    88. 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 »
    89. Ehlers-Danlos syndrome
     A group of inherited connective tissue disorders primarily involving the joints and skin. There are 11 disorders in the group....more »
    90. Ehlers-Danlos syndrome Type I
     A rare genetic connective tissue disorder characterized by hyperextensible joints, hyperextensible skin and poor wound healing....more »
    91. 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 »
    92. 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 »
    93. 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 »
    94. 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 »
    95. Ehlers-Danlos syndrome type V
     A rare genetic connective tissue disorder characterized by skin hyperextensibility, moderate joint hypermobility and moderate vascular fragility....more »
    96. 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 »
    97. 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 »
    98. 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 »
    99. 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 »
    100. Ehlers-Danlos syndrome, cardiac valvular form
     A rare genetic connective tissue disorder characterized by hypermobile joints, joint dislocations and skin hyperextensibility and fragility....more »
    101. 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 »
    102. 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 »
    103. 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 »
    104. 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 »
    105. 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 »
    106. Ehlers-Danlos syndrome, progeroid form 2
     A rare genetic connective tissue disorder characterized by hypermobile joints, fragile skin, mental retardation and short stature....more »
    107. Ehlers-Danlos syndrome, tenascin-X deficiency
     A rare genetic connective tissue disorder characterized by hypermobile joints, joint dislocations and skin hyperextensibility and fragility....more »
    108. 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 »
    109. Epidermolysis bullosa simplex, Ogna type
     An inherited skin blistering condition characterized by blisters on palms and soles....more »
    110. Epstein-Barr virus
     Common virus causing mononucleosis...more »
    111. Essential thrombocytopenia
     A rare blood disorder characterized by an excessively low number of platelets in the blood which often results in hemorrhages....more »
    112. 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 »
    113. 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 »
    114. 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 »
    115. 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 »
    116. 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 »
    117. 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 »
    118. 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 »
    119. 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 »
    120. 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 »
    121. 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 »
    122. 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 »
    123. 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 »
    124. 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 »
    125. 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 »
    126. 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 »
    127. 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 »
    128. 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 »
    129. 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 »
    130. 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 »
    131. 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 »
    132. 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 »
    133. 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 »
    134. 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 »
    135. 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 »
    136. 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 »
    137. 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 »
    138. 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 »
    139. 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 »
    140. 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 »
    141. 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 »
    142. 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 »
    143. 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 »
    144. 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 »
    145. 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 »
    146. 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 »
    147. 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 »
    148. 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 »
    149. Fanconi's syndrome
    150. Felty Syndrome
     A rare complication of long-term rheumatoid arthritis which involves an enlarged spleen and blood abnormalities....more »
    151. 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 »
    152. 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 »
    153. 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 »
    154. 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 »
    155. 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 »
    156. 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 »
    157. 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 »
    158. 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 »
    159. 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 »
    160. 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 »
    161. 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 »
    162. HIV/AIDS
     HIV is a sexually transmitted virus and AIDS is the progressive immune failure that HIV causes....more »
    163. Hairy cell leukemia
     A chronic leukemia which causes an excess of abnormal mononuclear cells which appear hair like under microscopy...more »
    164. 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 »
    165. 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 »
    166. 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 »
    167. 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 »
    168. 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 »
    169. Hemophilia A
     A rare coagulation disorder caused by a deficiency of factor VIII which results in bleeding problems....more »
    170. Hemophilia B
     A rare coagulation disorder caused by a deficiency of factor IX which results in bleeding problems....more »
    171. 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 »
    172. 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 »
    173. 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 »
    174. 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 »
    175. Hypersplenism
     A condition which is characterized by the exaggeration of blood degrading function of the spleen...more »
    176. Immune thrombocytopenia
     A rare disorder where the body's immune system attacks blood platelets which affect the blood's ability to clot....more »
    177. 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 »
    178. 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 »
    179. Kidney failure
     Total failure of the kidneys to filter waste...more »
    180. 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 »
    181. Leishmaniasis
     A rare infectious disease caused by any of a number of parasitic Leishmania species. Infection can cause any of three different manifestations: cutaneous leishmaniasis, mucosal leishmaniasis and visceral leishmaniasis....more »
    182. 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 »
    183. 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 »
    184. 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 »
    185. 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 »
    186. 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 »
    187. 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 »
    188. 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 »
    189. 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 »
    190. Leukemia, T-cell, chronic
     Cancer of blood cells called T-cells which form part of the immune system....more »
    191. Liver conditions
     Any condition that affects the liver...more »
    192. Lupus
     Autoimmune disease with numerous effects on various organs and linings....more »
    193. 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 »
    194. Lymphocytic leukemia
     A condition characterized by the proliferation of lymphoid tissues...more »
    195. Malaria
     A parasitic disease transmitted through mosquito bites....more »
    196. Marchiafava-Micheli disease
     A blood disorder where abnormalities in erhtyrocyte membranes results in excessive destruction of red blood cells and hence anemia....more »
    197. 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 »
    198. 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 »
    199. 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 »
    200. 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 »
    201. Multiple Myeloma
     A rare malignant cancer that occurs in the bone marrow. More common in skull, spine, rib cage, pelvis and legs....more »
    202. Myelodysplastic syndromes
     A group of syndromes characterized by a disruption in the production of blood cells. Often the bone marrow increases production of various blood cells but because many of them are defective, they are destroyed before the reach the blood stream....more »
    203. 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 »
    204. Myelofibrosis-osteosclerosis
     Formation of fibrous tissue in the bone marrow in response to bone marrow damage....more »
    205. Myelogenous leukemia
     A condition which is characterized proliferation of myeloid tissue and the abnormal increase in granulocytes...more »
    206. 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 »
    207. 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 »
    208. 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 »
    209. 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 »
    210. Non-Hodgkin's lymphoma, during pregnancy
     A cancer that originates in the lymphatic system and occurs during pregnancy. The greatest problem is the fact that the cancer is usually quite aggressive and delays in delivery often results in delayed treatment and a poor prognosis....more »
    211. 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 »
    212. Occupational Cancer -- Hematopoietic system cancer
     Occupational exposure to X-radiation can increase the risk of developing hematopoietic system cancer....more »
    213. Osteogenesis imperfecta Type I
     A rare genetic connective tissue disorder characterized by fragile bones, blue sclerae and hyperextensible joints....more »
    214. 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 »
    215. 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 »
    216. 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 »
    217. 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 »
    218. 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 »
    219. 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 »
    220. Philadelphia-negative chronic myeloid leukemia
     A form of leukemia....more »
    221. 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 »
    222. 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 »
    223. 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 »
    224. Retinopathy -- aplastic anemia -- neurological abnormalities
     A very rare syndrome characterized by retinal disease, aplastic anemia and neurological problems....more »
    225. 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 »
    226. 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 »
    227. 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 »
    228. 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 »
    229. Septicemia
     A systemic inflammatory response to an infection....more »
    230. 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 »
    231. Spondylometaphyseal dysplasia with combined immunodeficiency
     A rare syndrome characterized by skeletal abnormalities as well as a poor immune system....more »
    232. 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 »
    233. 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 »
    234. 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 »
    235. 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 »
    236. 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 »
    237. Thalidomide -- Teratogenic Agent
     There is evidence to indicate that exposure to Thalidomide 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 »
    238. 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 »
    239. Thrombasthenia
     An inherited blood clotting disorder where abnormal blood platelet function causes results in excessive bleeding....more »
    240. Thrombocytopathy
     A blood disorder where abnormal blood platelets affect blood coagulation....more »
    241. Thrombocytopenia -- cerebellar hypoplasia -- short stature
     A very rare syndrome characterized mainly by short stature, low blood platelets and abnormal brain development....more »
    242. Type I Glycogen Storage Disease
     A condition which is characterized by a disease affecting glycogen storage...more »
    243. Typhoid fever
     Fever from bacterial food poisoning....more »
    244. Viral diseases
     Any disease that is caused by a virus...more »
    245. 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 »
    246. 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 »
    247. 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 »
    248. 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 »
    249. Waldenstrom macroglobulinemia
     A rare disorder involving malignancy of the lymph and blood cells....more »
    250. Wilson's Disease
     Wilson disease, or hepatolenticular degeneration, is a neurodegenerative disease of copper metabolism....more »
    251. 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 »
    252. 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 »
    253. 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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