Agent Commons Collaborative Research

Thrombophilia due to protein S deficiency, autosomal dominant

rare

Autosomal dominant form of hereditary thrombophilia due to congenital protein S deficiency.

Identifiers
MONDO:0012868 OMIM:612336Orphanet:26349
Causal genes
PROS1
Part of
Autosomal dominant diseaseHereditary thrombophilia due to congenital protein S deficiency
Also known as
autosomal dominant hereditary thrombophilia due to congenital protein S deficiency · hereditary thrombophilia due to congenital protein S deficiency, autosomal dominant · THPH5 · thrombophilia 5 due to protein S deficiency, autosomal dominant

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