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 ]

This is just here as a test because I lose it

Term information

database cross reference
  • 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)
Subsets

ordo_disease

abbreviation
ITP [ Orphanet:3002 ]

closeMatch

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

definition

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.

exactMatch

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

has exact synonym

idiopathic thrombocytopenic purpura

ITP

immune thrombocytopenia

idiopathic thrombocytopenia purpura

idiopathic thrombocytopenia

primary thrombocytopenic purpura

autoimmune thrombocytopenic purpura

thrombocytopenic purpura, autoimmune

has related synonym

thrombocytopenic purpura autoimmune

werlhof's disease

immune thrombocytopenic purpura

idiopathic purpura

Ideopath thrombocytopenic pur

AITP

id

MONDO:0008558