Term Name: autosomal dominant thrombophilia due to protein S deficiency
Synonyms: THPH5
Definition: A protein S deficiency characterized by reduced serum protein S levels and recurrent venous thrombosis that has_material_basis_in heterozygous mutation in the PROS1 gene on chromosome 3q11.1.
Ontology: Human Disease [DOID:0111900]   ( DOID:0111900 )

Relationships
is a type of: autosomal dominant disease protein S deficiency