Hereditary Factor III Deficiency

Preferred Label : Hereditary Factor III Deficiency;

NCIt related terms : Hereditary Tissue Factor Deficiency;

Alternative definition : NICHD: An autosomal recessive, inherited coagulation disorder characterized by the partial or complete absence of tissue factor (factor III) activity in the blood.;

NCI Metathesaurus CUI : CL514653;

Details

Origin ID

C131644;

UMLS CUI

C4330257;

Has associated anatomic sites
- Hematopoietic and Lymphatic System [NCIt concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
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- NICHD Terminology [NCIt concept]
- Pediatric Hematology-Oncology Terminology [NCIt concept]
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- Hematopoietic and Lymphoid Cell [NCIt concept]
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- Hematopoietic and Lymphoid Tissue [NCIt concept]
disease_has_primary_anatomic_site
- Hematopoietic and Lymphatic System [NCIt concept]
disease_mapped_to_gene
- F3 Gene [NCIt concept]

Keyword's position in hierarchy(ies) :

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