Immune thrombocytopenia

Preferred Label : Immune thrombocytopenia;

Symbol : ITP;

CISMeF acronym : AITP; ITP;

Type : Other, mainly phenotypes with suspected mendelian basis;

Alternative titles and symbols : Immune thrombocytopenic purpura; ITP; Idiopathic thrombocytopenic purpura; AITP; Thrombocytopenic purpura, autoimmune;

Description : Autoimmune thrombocytopenic purpura is characterized by a low platelet count, normal bone marrow, and the absence of other causes of thrombocytopenia. It is principally a disorder of increased platelet destruction mediated by autoantibodies to platelet-membrane antigens (George et al., 1994).;

Inheritance : Autosomal dominant form;

Prefixed ID : 188030;

Details

Origin ID

188030;

UMLS CUI

C0398650;

Automatic exact mappings (from CISMeF team)
- Acute idiopathic thrombocytopenic purpura (disorder) [SNOMED CT concept]
- Autoimmune thrombocytopenia [HPO term]
- Chronic idiopathic thrombocytopenic purpura (disorder) [SNOMED CT concept]
- Immune thrombocytopenic purpura [MedDRA LLT]
- Immune thrombocytopenic purpura [ICD-9 code]
- autoimmune thrombocytopenic purpura [DO Concept]
- autoimmune thrombocytopenic purpura [Blood Transfusion thesaurus concept]
- inosine 5'-(tetrahydrogen triphosphate) [Substance BNPC]
- inosine triphosphate [MeSH Descriptor]
- inosine triphosphate [MeSH concept]
Currated CISMeF NLP mapping
- Idiopathic thrombocytopenic purpura [PASCAL descriptor]
- Idiopathic thrombocytopenic purpura [MedDRA LLT]
- Idiopathic thrombocytopenic purpura [ICD-10 Sub-category (who)]
- Immune thrombocytopenia [ORDO Disease]
- Immune thrombocytopenic purpura [PASCAL descriptor]
- Immune thrombocytopenic purpura [ICD-10 Sub-category]
- Immune thrombocytopenic purpura [ICD-11 Sub-sub category]
- Immune thrombocytopenic purpura (disorder) [Inactive SNOMED CT concept]
- Immune thrombocytopenic purpura (disorder) [SNOMED CT concept]
- Primary Immune Thrombocytopenia [NCIt concept]
- idiopathic thrombocytopenic purpura [Disease (Nov.)]
- idiopathic thrombocytopenic purpura [HPO term]
- idiopathic thrombocytopenic purpura, nos [SNOMED Notion]
- purpura, thrombocytopenic, idiopathic [MeSH Descriptor]
- purpura, thrombocytopenic, idiopathic [MeSH concept]
DO Cross reference
- autoimmune thrombocytopenic purpura [DO Concept]
HPO term(s)
- Abnormal bleeding [HPO term]
- Autosomal dominant inheritance [HPO term]
- Platelet antibody positive [HPO term]
- Thrombocytopenia [HPO term]
ORDO concept(s)
- Immune thrombocytopenia [ORDO Disease]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Idiopathic purpura [MedDRA LLT]
- Idiopathic thrombocytopenic purpura [MedDRA LLT]
- Idiopathic thrombocytopenic purpura [PASCAL descriptor]
- Immune thrombocytopenia [ORDO Disease]
- Immune thrombocytopenic purpura [MedDRA Preferred Term]
- Immune thrombocytopenic purpura [ICD-10 Sub-category]
- Immune thrombocytopenic purpura [ICD-9 code]
- Immune thrombocytopenic purpura [PASCAL descriptor]
- Immune thrombocytopenic purpura [MedDRA LLT]
- Immune thrombocytopenic purpura (disorder) [SNOMED CT concept]
- Immune thrombocytopenic purpura (disorder) [Inactive SNOMED CT concept]
- Primary Immune Thrombocytopenia [NCIt concept]
- Primary immune thrombocytopenia [MedDRA LLT]
- Werlhof's syndrome [MedDRA LLT]
- autoimmune thrombocytopenic purpura [DO Concept]
- idiopathic thrombocytopenic purpura [Disease (Nov.)]
- idiopathic thrombocytopenic purpura, nos [SNOMED Notion]
- purpura, thrombocytopenic, idiopathic [MeSH Descriptor]
- purpura, thrombocytopenic, idiopathic [MeSH concept]

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