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Summary Literature (0)
MIM:612336 - THROMBOPHILIA DUE TO PROTEIN S DEFICIENCY, AUTOSOMAL DOMINANT; THPH5

Xenbase Genes: pros1

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0012868 - thrombophilia due to protein S deficiency, autosomal dominant
MONDO:0019144 - hereditary thrombophilia due to congenital protein S deficiency

Disease Ontology (DO):
DOID:0111900 - autosomal dominant thrombophilia due to protein S deficiency