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- NCIT_C84904 IAO_0000115 "A rare autosomal dominant inherited disorder caused by mutations in the FGFR3 gene. It is characterized by premature fusion of cranial bones, resulting in head shape abnormalities, flattened cheekbones, and wide-set eyes." @default.
- NCIT_C84904 NCIT_NHC0 "C84904" @default.
- NCIT_C84904 NCIT_P106 "Disease or Syndrome" @default.
- NCIT_C84904 NCIT_P108 "Muenke Syndrome" @default.
- NCIT_C84904 NCIT_P207 "C1864436" @default.
- NCIT_C84904 NCIT_P322 "Cellosaurus" @default.
- NCIT_C84904 NCIT_R176 NCIT_C16612 @default.
- NCIT_C84904 NCIT_R176 NCIT_C19930 @default.
- NCIT_C84904 NCIT_R176 NCIT_C20103 @default.
- NCIT_C84904 NCIT_R176 NCIT_C20719 @default.
- NCIT_C84904 NCIT_R176 NCIT_C21281 @default.
- NCIT_C84904 NCIT_R176 NCIT_C21295 @default.
- NCIT_C84904 NCIT_R176 NCIT_C24393 @default.
- NCIT_C84904 NCIT_R176 NCIT_C25870 @default.
- NCIT_C84904 NCIT_R176 NCIT_C25871 @default.
- NCIT_C84904 NCIT_R176 NCIT_C25872 @default.
- NCIT_C84904 normalizedInformationContent "100" @default.
- NCIT_C84904 referenceCount "1" @default.
- NCIT_C84904 hasExactSynonym "FGFR3-Related Craniosynostosis" @default.
- NCIT_C84904 hasExactSynonym "Muenke Syndrome" @default.
- NCIT_C84904 inSubset NCIT_C165258 @default.
- NCIT_C84904 inSubset NCIT_C192842 @default.
- NCIT_C84904 type Class @default.
- NCIT_C84904 isDefinedBy ncit.owl @default.
- NCIT_C84904 label "Muenke Syndrome" @default.
- NCIT_C84904 subClassOf B3259d11e2ae791b8d890dc2a8a18f399 @default.
- NCIT_C84904 subClassOf B4f779f663e3757b4c8e2084be363c8b2 @default.
- NCIT_C84904 subClassOf NCIT_C28193 @default.
- NCIT_C84904 subClassOf NCIT_C2991 @default.
- NCIT_C84904 subClassOf NCIT_C4873 @default.
- NCIT_C84904 subClassOf NCIT_C53529 @default.
- NCIT_C84904 subClassOf NCIT_C53543 @default.
- NCIT_C84904 subClassOf NCIT_C53547 @default.
- NCIT_C84904 subClassOf NCIT_C7057 @default.
- NCIT_C84904 subClassOf NCIT_C84904 @default.