Primary Immune Thrombocytopenia

Preferred Label : Primary Immune Thrombocytopenia;

NCIt synonyms : Idiopathic Thrombocytopenia; Idiopathic Thrombocytopenia Purpura; ITP; Idiopathic Thrombocytopenic Purpura;

NCIt related terms : Immune thrombocytopenic purpura; Immune Thrombocytopenia;

NCIt definition : Acquired thrombocytopenia of unknown cause, characterized by immune-mediated destruction of normal platelets. It affects both children and adults. It manifests with petechiae, purpura, and overt bleeding. Based upon the duration of the disease, it is classified as newly diagnosed (from diagnosis until 3 months), persistent (3-12 months), and chronic (lasting for more than 12 months).;

Alternative definition : NCI-GLOSS: A condition in which platelets (blood cells that cause blood clots to form) are destroyed by the immune system. The low platelet count causes easy bruising and bleeding, which may be seen as purple areas in the skin, mucous membranes, and outer linings of organs.; NICHD: Disorder characterized by abnormally low level of circulating platelets, usually with normal hemoglobin/red blood cell and white blood cell levels, and thought to be secondary to autoimmune destruction.;

Codes from synonyms : CDR0000559453; CDR0000589406; CDR0000589407; D69.3;

Details

Origin ID

C3446;

UMLS CUI

C0398650;

Currated CISMeF NLP mapping
- Idiopathic thrombocytopenia [HPO term]
- Idiopathic thrombocytopenia [MedDRA LLT]
- Idiopathic thrombocytopenic purpura [PASCAL descriptor]
- Idiopathic thrombocytopenic purpura [MedDRA LLT]
- Idiopathic thrombocytopenic purpura [ICD-10 Sub-category (who)]
- Immune thrombocytopenia [OMIM Phenotype]
- Immune thrombocytopenia [ORDO Disease]
- Immune thrombocytopenic purpura [ICD-10 Sub-category]
- Immune thrombocytopenic purpura [PASCAL descriptor]
- Immune thrombocytopenic purpura [MedDRA Preferred Term]
- Immune thrombocytopenic purpura [ICD-11 Sub-sub category]
- Immune thrombocytopenic purpura (disorder) [SNOMED CT concept]
- Primary immune thrombocytopenia [MedDRA LLT]
- 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]
False automatic mappings
- Immune thrombocytopenic purpura (disorder) [Inactive SNOMED CT concept]
Has associated anatomic sites
- Hematopoietic and Lymphatic System [NCIt concept]
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 [OMIM Phenotype]
- Immune thrombocytopenia [ORDO Disease]
- Immune thrombocytopenic purpura [MedDRA Preferred Term]
- Immune thrombocytopenic purpura [ICD-10 Sub-category]
- Immune thrombocytopenic purpura [PASCAL descriptor]
- Immune thrombocytopenic purpura [ICD-9 code]
- Immune thrombocytopenic purpura [MedDRA LLT]
- Immune thrombocytopenic purpura (disorder) [Inactive SNOMED CT concept]
- Immune thrombocytopenic purpura (disorder) [SNOMED CT 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]
concept_is_in_subset
- CTRP Disease Terminology [NCIt concept]
- CTRP Terminology [NCIt concept]
- Cellosaurus Disease Terminology [NCIt concept]
- Cellosaurus Terminology [NCIt concept]
- GDC Terminology [NCIt concept]
- GDC Value Terminology [NCIt concept]
- NICHD Terminology [NCIt concept]
- Pediatric Adverse Events Terminology [NCIt concept]
- Pediatric Adverse Events Terminology Mapped to MedDRA [NCIt concept]
- Pediatric Hematology-Oncology Terminology [NCIt concept]
- SeroNet Authorized Values [NCIt concept]
- SeroNet Study Descriptors [NCIt concept]
- mCode Elixhauser Coagulation Deficiency Value Set [NCIt concept]
- mCode Terminology [NCIt concept]
disease_has_normal_cell_origin
- Hematopoietic and Lymphoid Cell [NCIt concept]
disease_has_normal_tissue_origin
- Hematopoietic and Lymphoid Tissue [NCIt concept]
disease_has_primary_anatomic_site
- Hematopoietic and Lymphatic System [NCIt concept]

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