combined deficiency of vitamin K-dependent clotting factors 2

Term ID

DOID:0112174

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
MIM: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 Pages

Alliance (1)

Genes Involved

Zebrafish Models