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 idiopathic thrombocytopenia purpura idiopathic thrombocytopenia thrombocytopenic purpura, autoimmune primary thrombocytopenic purpura autoimmune thrombocytopenic purpura
Term information
- OMIM:188030 (Orphanet:3002/e)
- EFO:0007160 (MONDO:equivalentTo)
- NANDO:2200645 (https://orcid.org/0000-0003-0011-764X)
- GARD:5194 (MONDO:GARD)
- ICD9:287.31 (DOID:8924)
- NCIT:C3446 (MONDO:equivalentTo)
- DOID:8924 (MONDO:equivalentTo)
- icd11.foundation:364346400 (https://orcid.org/0000-0001-5208-3432)
- MEDGEN:584986 (MONDO:equivalentTo)
- UMLS:C0398650 (MONDO:equivalentTo)
- Orphanet:3002 (OMIM:188030)
- MedDRA:10021245 (Orphanet:3002/e)
- NANDO:1200315 (https://orcid.org/0000-0003-0011-764X)
ordo_disorder, matrix_llm__is_cancer_other, gard_rare, mondo_top_grouping_member, matrix_llm__txgnn_other, harrisons_view_immune_system_disorder, nord_rare, matrix_included, matrix_txgnn_grouping_member, mondo_top_grouping_immune_system_disorder, rare, orphanet_rare, matrix_txgnn_grouping_autoimmune_disease, matrix_llm__is_glucose_dysfunction_other, otar, mondo_top_grouping_hematologic_disorder, matrix_llm__tag_qualy_lost_other, matrix_llm__medical_specialization_other, mondo_top_grouping_hereditary_disease, matrix_llm__tag_existing_treatment_other, matrix_llm__anatomical_other, matrix_llm__is_pathogen_caused_other, harrisons_view_hematologic_disorder, harrisons_view_member, harrisons_view_hereditary_disease
http://purl.obolibrary.org/obo/DOID_8924
http://identifiers.org/medgen/584986
http://purl.obolibrary.org/obo/NCIT_C3446
http://www.ebi.ac.uk/efo/EFO_0007160
https://omim.org/entry/188030
http://linkedlifedata.com/resource/umls/id/C0398650
http://www.orpha.net/ORDO/Orphanet_3002
http://purl.obolibrary.org/obo/mondo/sources/icd11foundation/364346400
thrombocytopenic purpura autoimmune
immune thrombocytopenic purpura
idiopathic purpura
AITP
ideopath thrombocytopenic pur
Werlhof's disease
Term relations
- [X] primary thrombocytopenia
- [X] inherited bleeding disorder, platelet-type
- [X] thrombocytopenic purpura
- [X] inherited thrombocytopenia
- [X] inherited blood coagulation disorder
- [X] autoimmune thrombocytopenia
- disease has location some platelet
- has material basis in germline mutation in some FCGR2C