ZFIN Human Disease: combined deficiency of vitamin K-dependent clotting factors 1

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 the GGCX gene on chromosome 2p11.2. https://pubmed.ncbi.nlm.nih.gov/9845520/
References:	MESH:C564741 OMIM:277450 UMLS_CUI:C1848534
Ontology:	Human Disease ( DOID:0112173 )

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 1 PAGES

Alliance (1)

GENES INVOLVED

Human Gene	Zebrafish Ortholog	OMIM Term	OMIM Phenotype ID
GGCX	ggcx	Vitamin K-dependent clotting factors, combined deficiency of, 1	277450

ZEBRAFISH MODELS No data available

PHENOTYPE No data available

CITATIONS: None