OBO ID: DOID:0111901
Term Name: heparin cofactor II deficiency Search Ontology:
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. (2)
References:
Ontology: Human Disease   ( DOID:0111901 )
OTHER heparin cofactor II deficiency PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
SERPIND1 Thrombophilia 10 due to heparin cofactor II deficiency 612356
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None