Afibrinogenemia

Preferred Label : Afibrinogenemia;

NCIt definition : A blood coagulation disorder characterized by the complete absence of fibrinogen in the blood, resulting in bleeding.;

Details

Origin ID

C98130;

UMLS CUI

C0001733;

Automatic exact mappings (from CISMeF team)
- Afibrinogenemia [PASCAL descriptor]
- Other specified coagulation defects [ICD-10 Sub-category (who)]
- afibrinogenemia [Blood Transfusion thesaurus concept]
Currated CISMeF NLP mapping
- Afibrinogenaemia [MedDRA LLT]
- Afibrinogenemia [MedDRA LLT]
- Afibrinogenemia (disorder) [SNOMED CT concept]
- afibrinogenemia [MeSH Descriptor]
- afibrinogenemia [MeSH concept]
- blood clotting factor i deficiency [Disease (Nov.)]
DO Cross reference
- congenital afibrinogenemia [DO Concept]
Has associated anatomic sites
- Hematopoietic and Lymphatic System [NCIt concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Afibrinogenaemia [MedDRA LLT]
- Afibrinogenemia [MedDRA LLT]
- Afibrinogenemia (disorder) [SNOMED CT concept]
- afibrinogenemia [MeSH concept]
- afibrinogenemia [MeSH Descriptor]
- congenital afibrinogenemia [DO 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]

Keyword's position in hierarchy(ies) :

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