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Summary Literature (0)
MIM:176860 - THROMBOPHILIA DUE TO PROTEIN C DEFICIENCY, AUTOSOMAL DOMINANT; THPH3

Xenbase Genes: proc, proc.2

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0008316 - thrombophilia due to protein C deficiency, autosomal dominant
MONDO:0019145 - hereditary thrombophilia due to congenital protein C deficiency

Disease Ontology (DO):
DOID:0111909 - autosomal dominant thrombophilia due to protein C deficiency
DOID:3756 - protein C deficiency