OBO ID: DOID:0111901 |
Term Name: | heparin cofactor II deficiency | Search Ontology: | |
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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) | ||
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Ontology: | Human Disease ( DOID:0111901 ) |
OTHER heparin cofactor II deficiency PAGES
ZEBRAFISH MODELS
No data available
PHENOTYPE
No data available
CITATIONS: None
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