Hereditary Coagulation Factor Deficiency

Preferred Label : Hereditary Coagulation Factor Deficiency;

NCIt related terms : Hereditary deficiency of Other clotting factors;

NCIt definition : An inherited blood coagulation disorder characterized by deficiency of one of the coagulation factors, resulting in bleeding.;

Alternative definition : NICHD: An inherited coagulation disorder characterized by deficiency of one of the coagulation factors.;

Codes from synonyms : D68.2;

Details

Origin ID

C98942;

UMLS CUI

C0272316;

Automatic exact mappings (from CISMeF team)
- Hereditary coagulation factor deficiency (disorder) [SNOMED CT concept]
- hereditary coagulation factor deficiency, nos [SNOMED Notion]
Has associated anatomic sites
- Hematopoietic and Lymphatic System [NCIt concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Hereditary coagulation factor deficiency (disorder) [SNOMED CT concept]
- hereditary coagulation factor deficiency, nos [SNOMED Notion]
concept_is_in_subset
- NICHD Terminology [NCIt concept]
- Neonatal Research Network Terminology [NCIt concept]
- Pediatric Hematology-Oncology Terminology [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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