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DO Term : protein C deficiency [DOID:3756] Disease Ontology
Namespace  disease_ontology Obsolete  false
description  A thrombophilia that is characterized by recurrent venous thrombosis and that has_material_basis_in heterozygous mutation in the PROC gene on chromosome 2q14.
  • synonyms:
  • NCI:C99025,
  • SNOMEDCT_US_2023_03_01:76407009,
  • MESH:D020151,
  • GARD:4521,
  • ORDO:745,
  • UMLS_CUI:C0398625,
  • ICD10CM:D68.59
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Disease

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Ontology

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Ontology Term --> Direct parents





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