Concept information
Preferred term
Purpura, Thrombotic Thrombocytopenic
Type
-
Topical Descriptor
Broader concept
Entry terms
- Moschcowitz Disease
- Moschkowitz Disease
- Purpura, Thrombotic Thrombopenic
- Thrombopenic Purpura, Thrombotic
- Thrombotic Thrombocytopenic Purpura
- Thrombotic Thrombopenic Purpura
Scope note
- An acquired, congenital, or familial disorder caused by PLATELET AGGREGATION with THROMBOSIS in terminal arterioles and capillaries. Clinical features include THROMBOCYTOPENIA; HEMOLYTIC ANEMIA; AZOTEMIA; FEVER; and thrombotic microangiopathy. The classical form also includes neurological symptoms and end-organ damage, such as RENAL FAILURE. Mutations in the ADAMTS13 PROTEIN gene have been identified in familial cases.
History note
- 1986; use PURPURA, THROMBOTIC THROMBOPENIC 1965-1985
In other languages
-
Finnish
-
microangiopathia thrombotica
-
Moschcowitz
-
Moschcowitzin oireyhtymä
-
Moschcowitzin sairaus
-
Moschcowitzin syndrooma
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Moschcowitzin tauti
-
purpura thrombocytopenica thrombotica
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tromboottinen mikroangiopatia
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trombosytopeeninen tromboottinen purppura
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TTP
-
Swedish
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Familjär trombotisk mikroangiopati
-
Moschcowitz sjukdom
-
Upshaw-Schulman syndrom
URI
http://www.yso.fi/onto/mesh/D011697
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