OBO ID: DOID:0112174
Term Name: combined deficiency of vitamin K-dependent clotting factors 2 Search Ontology:
Synonyms:
  • VKCFD2
Definition: A hereditary combined deficiency of vitamin K-dependent clotting factors that has_material_basis_in homozygous or compound heterozygous mutation in VKORC1 on chromosome 16p11.2. https://pubmed.ncbi.nlm.nih.gov/14765194/
References:
Ontology: Human Disease   (DOID:0112174)
OTHER combined deficiency of vitamin K-dependent clotting factors 2 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
VKORC1 Vitamin K-dependent clotting factors, combined deficiency of, 2 607473
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None