OBO ID: DOID:0112173 |
Term Name: | combined deficiency of vitamin K-dependent clotting factors 1 | Search Ontology: | |
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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/ | ||
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Ontology: | Human Disease ( DOID:0112173 ) |
OTHER combined deficiency of vitamin K-dependent clotting factors 1 PAGES
ZEBRAFISH MODELS
No data available
PHENOTYPE
No data available
CITATIONS: None
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