Term Name: heparin cofactor II deficiency
Synonyms: HCF 2 deficiency, HCF II deficiency, THPH10, thrombophilia due to heparin cofactor II deficiency
Definition: A thrombophilia characterized by increased risk of thromboembolism that has_material_basis_in heterozygous mutation in the HCF2 gene on chromosome 22q11.21.
Ontology: Human Disease [DOID:0111901]   ( DOID:0111901 )

Relationships
is a type of: autosomal dominant disease thrombophilia