thrombotic thrombocytopenic purpura
Go to external page http://purl.obolibrary.org/obo/MONDO_0018896
Thrombotic thrombocytopenic purpura (TTP) is an aggressive and life-threatening form of thrombotic microangiopathy (TMA) characterized by profound peripheral thrombocytopenia, microangiopathic hemolytic anemia (MAHA) and organ failure of variable severity and is comprised of congenital TTP and acquired TTP. [ Orphanet:54057 ]
Term information
- ICD10:M31.1 (Orphanet:54057)
- SCTID:78129009 (MONDO:equivalentTo)
- MedDRA:10043648 (Orphanet:54057)
- MESH:D011697 (Orphanet:54057)
- UMLS:C0034155 (Orphanet:54057)
- Orphanet:54057 (MONDO:equivalentTo)
- DOID:10772 (MONDO:equivalentTo)
- NCIT:C78797 (MONDO:equivalentTo)
- COHD:4301602 (MONDO:equivalentTo)
ordo_disease
http://identifiers.org/snomedct/360402008
http://identifiers.org/snomedct/195358008
http://identifiers.org/snomedct/195359000
http://identifiers.org/snomedct/155443009
Thrombotic thrombocytopenic purpura (TTP) is an aggressive and life-threatening form of thrombotic microangiopathy (TMA) characterized by profound peripheral thrombocytopenia, microangiopathic hemolytic anemia (MAHA) and organ failure of variable severity and is comprised of congenital TTP and acquired TTP.
http://identifiers.org/meddra/10043648
http://purl.obolibrary.org/obo/NCIT_C78797
http://www.orpha.net/ORDO/Orphanet_54057
http://linkedlifedata.com/resource/umls/id/C0034155
http://identifiers.org/mesh/D011697
http://identifiers.org/snomedct/78129009
http://purl.obolibrary.org/obo/DOID_10772