protein C deficiency Disease Ontology Browser

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Disease Ontology Browser

protein C deficiency (DOID:3756)
Alliance: disease page
Alt IDs: ICD10CM:D68.59, MESH:D020151, NCI:C99025, ORDO:745, UMLS_CUI:C0398625
Definition: A thrombophilia that is characterized by recurrent venous thrombosis and that has_material_basis_in heterozygous mutation in the PROC gene on chromosome 2q14.

Contributing Projects: Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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