OBO ID: DOID:0112173
Term Name: combined deficiency of vitamin K-dependent clotting factors 1 Search Ontology:
Synonyms:
  • VKCFD1
Definition: A hereditary combined deficiency of vitamin K-dependent clotting factors that has_material_basis_in homozygous or compound heterozygous mutation in GGCX on chromosome 2p11.2. https://pubmed.ncbi.nlm.nih.gov/9845520/
References:
Ontology: Human Disease   (DOID:0112173)
OTHER combined deficiency of vitamin K-dependent clotting factors 1 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
GGCX Vitamin K-dependent clotting factors, combined deficiency of, 1 277450
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None