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- NCIT_C103144 IAO_0000115 "A rare, autosomal recessive syndrome characterized by the presence of polyhydramnios, neonatal macrosomia, craniofacial abnormalities, nephroblastomatosis, and predisposition to Wilms tumor. The prognosis is poor." @default.
- NCIT_C103144 NCIT_A13 NCIT_C177171 @default.
- NCIT_C103144 NCIT_NHC0 "C103144" @default.
- NCIT_C103144 NCIT_P106 "Disease or Syndrome" @default.
- NCIT_C103144 NCIT_P108 "Perlman Syndrome" @default.
- NCIT_C103144 NCIT_P207 "C0796113" @default.
- NCIT_C103144 NCIT_P322 "CCPS" @default.
- NCIT_C103144 NCIT_P322 "Cellosaurus" @default.
- NCIT_C103144 NCIT_R176 NCIT_C16612 @default.
- NCIT_C103144 NCIT_R176 NCIT_C177171 @default.
- NCIT_C103144 NCIT_R176 NCIT_C21281 @default.
- NCIT_C103144 NCIT_R176 NCIT_C25804 @default.
- NCIT_C103144 NCIT_R176 NCIT_C25952 @default.
- NCIT_C103144 NCIT_R176 NCIT_C25953 @default.
- NCIT_C103144 normalizedInformationContent "100" @default.
- NCIT_C103144 referenceCount "1" @default.
- NCIT_C103144 hasExactSynonym "Perlman Syndrome" @default.
- NCIT_C103144 hasExactSynonym "Renal Hamartomas, Nephroblastomatosis and Fetal Gigantism" @default.
- NCIT_C103144 inSubset NCIT_C165258 @default.
- NCIT_C103144 inSubset NCIT_C177281 @default.
- NCIT_C103144 inSubset NCIT_C177516 @default.
- NCIT_C103144 inSubset NCIT_C192842 @default.
- NCIT_C103144 type Class @default.
- NCIT_C103144 isDefinedBy ncit.owl @default.
- NCIT_C103144 label "Perlman Syndrome" @default.
- NCIT_C103144 subClassOf Ba2bbc0464fcda268642cb04a8ba30842 @default.
- NCIT_C103144 subClassOf Bbfebdc7017a7d9049e2adfda58ac2384 @default.
- NCIT_C103144 subClassOf NCIT_C103144 @default.
- NCIT_C103144 subClassOf NCIT_C28193 @default.
- NCIT_C103144 subClassOf NCIT_C2991 @default.
- NCIT_C103144 subClassOf NCIT_C7057 @default.