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- NCIT_C75464 IAO_0000115 "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.
- NCIT_C75464 NCIT_NHC0 "C75464" @default.
- NCIT_C75464 NCIT_P106 "Disease or Syndrome" @default.
- NCIT_C75464 NCIT_P108 "Polycystic Kidney Disease" @default.
- NCIT_C75464 NCIT_P207 "C0022680" @default.
- NCIT_C75464 NCIT_P322 "Cellosaurus" @default.
- NCIT_C75464 NCIT_P322 "NICHD" @default.
- NCIT_C75464 NCIT_P325 "An inherited form of kidney disease characterized by multiple renal cysts." @default.
- NCIT_C75464 NCIT_P366 "Polycystic_Kidney_Disease" @default.
- NCIT_C75464 NCIT_R100 NCIT_C12219 @default.
- NCIT_C75464 NCIT_R100 NCIT_C12413 @default.
- NCIT_C75464 NCIT_R100 NCIT_C12415 @default.
- NCIT_C75464 NCIT_R100 NCIT_C12810 @default.
- NCIT_C75464 NCIT_R100 NCIT_C12919 @default.
- NCIT_C75464 NCIT_R100 NCIT_C13018 @default.
- NCIT_C75464 NCIT_R101 NCIT_C12219 @default.
- NCIT_C75464 NCIT_R101 NCIT_C12413 @default.
- NCIT_C75464 NCIT_R101 NCIT_C12415 @default.
- NCIT_C75464 NCIT_R101 NCIT_C12810 @default.
- NCIT_C75464 NCIT_R101 NCIT_C12919 @default.
- NCIT_C75464 NCIT_R101 NCIT_C13018 @default.
- NCIT_C75464 normalizedInformationContent "84.76342111748103" @default.
- NCIT_C75464 referenceCount "10" @default.
- NCIT_C75464 hasExactSynonym "Fibrocystic Renal Disease" @default.
- NCIT_C75464 hasExactSynonym "PKD - Polycystic Kidney Disease" @default.
- NCIT_C75464 hasExactSynonym "Polycystic Kidney Disease" @default.
- NCIT_C75464 inSubset NCIT_C123272 @default.
- NCIT_C75464 inSubset NCIT_C165258 @default.
- NCIT_C75464 inSubset NCIT_C192842 @default.
- NCIT_C75464 inSubset NCIT_C90259 @default.
- NCIT_C75464 inSubset NCIT_C99147 @default.
- NCIT_C75464 type Class @default.
- NCIT_C75464 isDefinedBy ncit.owl @default.
- NCIT_C75464 label "Polycystic Kidney Disease" @default.
- NCIT_C75464 subClassOf NCIT_C156660 @default.
- NCIT_C75464 subClassOf NCIT_C156664 @default.
- NCIT_C75464 subClassOf NCIT_C27551 @default.
- NCIT_C75464 subClassOf NCIT_C27599 @default.
- NCIT_C75464 subClassOf NCIT_C27600 @default.
- NCIT_C75464 subClassOf NCIT_C2991 @default.
- NCIT_C75464 subClassOf NCIT_C3149 @default.
- NCIT_C75464 subClassOf NCIT_C3430 @default.
- NCIT_C75464 subClassOf NCIT_C34750 @default.
- NCIT_C75464 subClassOf NCIT_C53529 @default.
- NCIT_C75464 subClassOf NCIT_C53531 @default.
- NCIT_C75464 subClassOf NCIT_C7057 @default.
- NCIT_C75464 subClassOf NCIT_C75464 @default.