OBO ID: DOID:0111900 |
Term Name: | autosomal dominant thrombophilia due to protein S deficiency | Search Ontology: | |
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Definition: | A protein S deficiency characterized by reduced serum protein S levels and recurrent venous thrombosis that has_material_basis_in heterozygous mutation in the PROS1 gene on chromosome 3q11.1. (3) | ||
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Ontology: | Human Disease ( DOID:0111900 ) |
OTHER autosomal dominant thrombophilia due to protein S deficiency PAGES
ZEBRAFISH MODELS
No data available
PHENOTYPE
No data available
CITATIONS: None
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