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- NCIT_C153179 IAO_0000115 "An autosomal recessive condition caused by mutation(s) in the CRADD gene, encoding death domain-containing protein CRADD. It is characterized by mild to moderate intellectual disability and lissencephaly with anterior-predominant pachygyria." @default.
- NCIT_C153179 NCIT_NHC0 "C153179" @default.
- NCIT_C153179 NCIT_P106 "Disease or Syndrome" @default.
- NCIT_C153179 NCIT_P108 "Mental Retardation, Autosomal Recessive 34" @default.
- NCIT_C153179 NCIT_P207 "C3281044" @default.
- NCIT_C153179 NCIT_P322 "Cellosaurus" @default.
- NCIT_C153179 NCIT_R176 NCIT_C16612 @default.
- NCIT_C153179 NCIT_R176 NCIT_C190815 @default.
- NCIT_C153179 NCIT_R176 NCIT_C20348 @default.
- NCIT_C153179 NCIT_R176 NCIT_C20462 @default.
- NCIT_C153179 normalizedInformationContent "100" @default.
- NCIT_C153179 referenceCount "1" @default.
- NCIT_C153179 hasExactSynonym "MRT34" @default.
- NCIT_C153179 hasExactSynonym "Mental Retardation, Autosomal Recessive 34" @default.
- NCIT_C153179 hasExactSynonym "Mental Retardation, Autosomal Recessive 34, with Variant Lissencephaly" @default.
- NCIT_C153179 inSubset NCIT_C165258 @default.
- NCIT_C153179 inSubset NCIT_C192842 @default.
- NCIT_C153179 type Class @default.
- NCIT_C153179 isDefinedBy ncit.owl @default.
- NCIT_C153179 label "Mental Retardation, Autosomal Recessive 34" @default.
- NCIT_C153179 subClassOf B442caf7e3d514eef9920dcbb99bd58cc @default.
- NCIT_C153179 subClassOf Befe41ff10ce5533c89f4dad8888dbb54 @default.
- NCIT_C153179 subClassOf NCIT_C153179 @default.
- NCIT_C153179 subClassOf NCIT_C2991 @default.
- NCIT_C153179 subClassOf NCIT_C4873 @default.
- NCIT_C153179 subClassOf NCIT_C53529 @default.
- NCIT_C153179 subClassOf NCIT_C53543 @default.
- NCIT_C153179 subClassOf NCIT_C53547 @default.
- NCIT_C153179 subClassOf NCIT_C7057 @default.
- NCIT_C153179 subClassOf NCIT_C84392 @default.
- NCIT_C153179 subClassOf NCIT_C89328 @default.
- NCIT_C153179 subClassOf NCIT_C89330 @default.