All diseases

OMIM ID
274150
OMIM term:
THROMBOTIC THROMBOCYTOPENIC PURPURA, CONGENITAL; TTP
Alternative terms:
MICROANGIOPATHIC HEMOLYTIC ANEMIA
THROMBOTIC MICROANGIOPATHY, FAMILIAL
UPSHAW-SCHULMAN SYNDROME; USS
SCHULMAN-UPSHAW SYNDROME
UPSHAW FACTOR, DEFICIENCY OF
MICROANGIOPATHIC HEMOLYTIC ANEMIA, CONGENITAL
THROMBOTIC THROMBOCYTOPENIC PURPURA, FAMILIAL
(∗) Location:
9q34.2  
(†) Associated OMIM genes:
ADAMTS13  
(‡) Associated MGI genes:
Adamts13  

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