ZFIN Human Disease: combined deficiency of vitamin K-dependent clotting factors 2

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 the VKORC1 gene on chromosome 16p11.2. https://pubmed.ncbi.nlm.nih.gov/14765194/
References:	MESH:C564393 OMIM:607473
Ontology:	Human Disease ( DOID:0112174 )

Relationships

is a type of:	autosomal recessive disease hereditary combined deficiency of vitamin K-dependent clotting factors autosomal recessive disease hereditary combined deficiency of vitamin K-dependent clotting factors Show first 5 Terms

OTHER combined deficiency of vitamin K-dependent clotting factors 2 PAGES

Alliance (1)

GENES INVOLVED

Human Gene	Zebrafish Ortholog	OMIM Term	OMIM Phenotype ID
VKORC1	vkorc1	Vitamin K-dependent clotting factors, combined deficiency of, 2	607473

ZEBRAFISH MODELS No data available

PHENOTYPE No data available

CITATIONS: None