Source:http://linkedlifedata.com/resource/umls/id/C0015519
MSH: Blood coagulation disorder usually inherited as an autosomal recessive trait, though it can be acquired. It is characterized by defective activity in both the intrinsic and extrinsic pathways, impaired thromboplastin time, and impaired prothrombin consumption.,NCI: A rare autosomal recessive inherited blood coagulation disorder characterized by deficiency of factor X, resulting in bleeding.