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- B771d786d71bea21c89fd059c4903adb3 NCIT_P378 "NCI" @default.
- B771d786d71bea21c89fd059c4903adb3 type Axiom @default.
- B771d786d71bea21c89fd059c4903adb3 annotatedProperty IAO_0000115 @default.
- B771d786d71bea21c89fd059c4903adb3 annotatedSource NCIT_C75464 @default.
- B771d786d71bea21c89fd059c4903adb3 annotatedTarget "A usually autosomal dominant and less frequently autosomal recessive genetic disorder characterized by the presence of numerous cysts in the kidneys leading to end-stage renal failure. The autosomal dominant trait is associated with abnormalities on the short arm of chromosome 16. Symptoms in patients with the autosomal dominant trait usually appear at middle age and include abdominal pain, hematuria, and high blood pressure. Patients may develop brain aneurysms and liver cysts. Patients with the autosomal recessive trait present with progressive renal failure early in life and symptoms resulting from hepatic fibrosis. The autosomal recessive trait is associated with abnormalities of chromosome 6. Polycystic kidney disease may also result as a side effect in patients on renal dialysis." @default.