OBO ID: DOID:2235 |
Term Name: | prothrombin deficiency | Search Ontology: | |
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Definition: | A thrombophilia that is characterized by bleeding symptoms due to low levels of circulating prothrombin, and has_material_basis_in autosomal recessive inheritance of homozygous or compound heterozygous mutation in the gene encoding coagulation factor II, also known as prothrombin, on chromosome 11p11. (4) | ||
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Ontology: | Human Disease ( DOID:2235 ) |
OTHER prothrombin deficiency PAGES
ZEBRAFISH MODELS
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PHENOTYPE
No data available
CITATIONS: None
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