combined deficiency of vitamin K-dependent clotting factors 1

Term ID

DOID:0112173

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
MIM: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 Pages

Alliance (1)

Genes Involved

Zebrafish Models