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 ]
Synonyms: idiopathic thrombocytopenic purpura ITP immune thrombocytopenia idiopathic thrombocytopenia purpura idiopathic thrombocytopenia primary thrombocytopenic purpura autoimmune thrombocytopenic purpura thrombocytopenic purpura, autoimmune
Term information
- Orphanet:3002 (OMIM:188030)
- ICD9:287.31 (DOID:8924)
- EFO:0007160 (MONDO:equivalentTo)
- NCIT:C3446 (MONDO:equivalentTo)
- UMLS:C0398650 (MONDO:equivalentTo)
- MedDRA:10021245 (Orphanet:3002/e)
- MEDGEN:584986 (MONDO:equivalentTo)
- icd11.foundation:364346400 (https://orcid.org/0000-0001-5208-3432)
- GARD:5194 (MONDO:GARD)
- NANDO:2200645 (https://orcid.org/0000-0003-0011-764X)
- NANDO:1200315 (https://orcid.org/0000-0003-0011-764X)
- DOID:8924 (MONDO:equivalentTo)
- OMIM:188030 (Orphanet:3002/e)
gard_rare, ordo_disorder, otar, rare, nord_rare, orphanet_rare
http://purl.obolibrary.org/obo/DOID_8924
http://identifiers.org/medgen/584986
http://purl.obolibrary.org/obo/NCIT_C3446
https://omim.org/entry/188030
http://linkedlifedata.com/resource/umls/id/C0398650
http://www.orpha.net/ORDO/Orphanet_3002
thrombocytopenic purpura autoimmune
immune thrombocytopenic purpura
idiopathic purpura
AITP
ideopath thrombocytopenic pur
Werlhof's disease