autoimmune thrombocytopenic purpura
Go to external page http://purl.obolibrary.org/obo/MONDO_0008558
An autoimmune disorder in which the number of circulating platelets is reduced due to their antibody-mediated destruction. ITP is a diagnosis of exclusion and is heterogeneous in origin. [ NCIT:P378 ]
Term information
- OMIM:188030 (Orphanet:3002)
- Orphanet:3002 (OMIM:188030)
- NCIT:C3446 (MONDO:equivalentTo)
- ICD10:D69.3 (Orphanet:3002)
- COHD:4120621 (MONDO:equivalentTo)
- ICD9:287.31 (DOID:8924)
- GARD:0005194 (Orphanet-shared)
- EFO:0007160 (MONDO:equivalentTo)
- MedDRA:10021245 (Orphanet:3002)
- DOID:8924 (MONDO:equivalentTo)
ordo_disease
http://identifiers.org/snomedct/13172003
http://identifiers.org/snomedct/154825008
http://identifiers.org/snomedct/267567001
http://identifiers.org/snomedct/234490009
http://identifiers.org/snomedct/191315003
http://identifiers.org/snomedct/32273002
http://identifiers.org/snomedct/191316002
http://linkedlifedata.com/resource/umls/id/C0043117
http://linkedlifedata.com/resource/umls/id/C0920163
An autoimmune disorder in which the number of circulating platelets is reduced due to their antibody-mediated destruction. ITP is a diagnosis of exclusion and is heterogeneous in origin.
http://purl.obolibrary.org/obo/DOID_8924
http://identifiers.org/mesh/D016553
http://identifiers.org/omim/188030
http://purl.obolibrary.org/obo/NCIT_C3446
http://linkedlifedata.com/resource/umls/id/C0398650
http://www.orpha.net/ORDO/Orphanet_3002
http://identifiers.org/meddra/10021245
idiopathic thrombocytopenic purpura
ITP
immune thrombocytopenia
idiopathic thrombocytopenia purpura
idiopathic thrombocytopenia
primary thrombocytopenic purpura
autoimmune thrombocytopenic purpura
thrombocytopenic purpura, autoimmune
thrombocytopenic purpura autoimmune
werlhof's disease
immune thrombocytopenic purpura
idiopathic purpura
Ideopath thrombocytopenic pur
AITP