has characteristic has characteristic has material basis in germline mutation in ADAMTS13 inherited bleeding disorder, platelet-type kidney disorder congenital hematological disorder congenital thrombotic thrombocytopenic purpura https://github.com/monarch-initiative/mondo/issues/4069 https://github.com/monarch-initiative/mondo/issues/4521 https://www.malacards.org/card/thrombotic_thrombocytopenic_purpura_hereditary NANDO:1200317 GARD:0009430 familial TTP Upshaw-Schulman syndrome congenital TTP congenital thrombotic thrombocytopenic purpura MEDGEN:224783 MONDO:0010122 congenital ADAMTS-13 deficiency congenital ADAMTS13 deficiency thrombotic thrombocytopenic purpura, hereditary TTP SCTID:373420004 USS hereditary thrombotic thrombocytopenic purpura thrombotic thrombocytopenic purpura, congenital Microangiopathic hemolytic Anaemia UMLS:C1268935 Orphanet:93583 NCIT:C131657 ICD9:287.33 Congenital 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. TTP, congenital OMIM:274150 thrombotic thrombocytopenic purpura inherited inherited blood coagulation disorder inherited thrombocytopenia