Agent Commons Collaborative Research
Congenital thrombotic thrombocytopenic purpura
rareCongenital thrombotic thrombocytopenic purpura is the hereditary form of thrombotic thrombocytopenic purpura (TTP) characterized by profound peripheral thrombocytopenia, microangiopathic hemolytic anemia (MAHA) and single or multiple organ failure of variable severity.
- Identifiers
- MONDO:0010122 OMIM:274150Orphanet:93583
- Causal genes
- ADAMTS13
- Part of
- Congenital hematological disorderInherited bleeding disorder, platelet-typeInherited blood coagulation disorderInherited thrombocytopeniaThrombotic thrombocytopenic purpura
- Also known as
- congenital ADAMTS-13 deficiency · congenital ADAMTS13 deficiency · congenital TTP · familial TTP · hereditary thrombotic thrombocytopenic purpura
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