Autosomal dominant form of hereditary thrombophilia due to congenital protein S deficiency. The disease is thrombophilia due to protein S deficiency, autosomal dominant (MONDO_0012868, a Monarch Disease Ontology id). Also known as: autosomal dominant hereditary thrombophilia due to congenital protein S deficiency, hereditary thrombophilia due to congenital protein S deficiency, autosomal dominant, thrombophilia 5 due to protein S deficiency, autosomal dominant.