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

This is just here as a test because I lose it

Term information

database cross reference
  • 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)
Subsets

gard_rare, ordo_disorder, otar, rare, nord_rare, orphanet_rare

abbreviation
ITP [ Orphanet:3002 ]

closeMatch

http://identifiers.org/meddra/10021245

exactMatch

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

has related synonym

thrombocytopenic purpura autoimmune

immune thrombocytopenic purpura

idiopathic purpura

AITP

ideopath thrombocytopenic pur

Werlhof's disease

id

MONDO:0008558