Owren disease
Ow·ren dis·ease
(ō-ren), [MIM*227400]a congenital deficiency of factor V, resulting in prolongation of prothrombin time; bleeding and clotting times are consistently prolonged; autosomal recessive inheritance caused by mutation in the F5 gene on chromosome 1q.
Farlex Partner Medical Dictionary © Farlex 2012
Ow·ren dis·ease
(ō'ren di-zēz')A congenital deficiency of factor V, resulting in prolongation of prothrombin time; bleeding and clotting times are consistently prolonged; autosomal recessive inheritance caused by mutation in the F5 gene on chromosome 1q.
Medical Dictionary for the Health Professions and Nursing © Farlex 2012
Owren,
Paul Arnor, Norwegian hematologist, 1905–.Owren disease - congenital deficiency of factor V, resulting in prolongation of prothrombin time and coagulation time.
Medical Eponyms © Farlex 2012
Ow·ren dis·ease
(ō'ren di-zēz') [MIM*227400]A congenital deficiency of factor V, resulting in prolongation of prothrombin time; bleeding and clotting times are consistently prolonged.
Medical Dictionary for the Dental Professions © Farlex 2012