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Summary Literature (0)
MIM:614514 - THROMBOPHILIA DUE TO PROTEIN S DEFICIENCY, AUTOSOMAL RECESSIVE; THPH6

Xenbase Genes: pros1

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0013791 - thrombophilia due to protein S deficiency, autosomal recessive
MONDO:0019144 - hereditary thrombophilia due to congenital protein S deficiency

Disease Ontology (DO):
DOID:0111905 - autosomal recessive thrombophilia due to protein S deficiency