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- NCIT_C118697 IAO_0000115 "An autosomal dominant disorder that is often caused by a defect in fibroblast growth factor receptor 3, and characterized by short stature, micromelia, and a comparatively large head. The features are milder than those seen in achondroplasia." @default.
- NCIT_C118697 NCIT_NHC0 "C118697" @default.
- NCIT_C118697 NCIT_P106 "Disease or Syndrome" @default.
- NCIT_C118697 NCIT_P108 "Hypochondroplasia" @default.
- NCIT_C118697 NCIT_P207 "C0410529" @default.
- NCIT_C118697 NCIT_P322 "Cellosaurus" @default.
- NCIT_C118697 NCIT_P322 "NICHD" @default.
- NCIT_C118697 NCIT_P325 "A condition phenotypically similar to, but milder than, achondroplasia that is often caused by mutations in the FGFR3 gene." @default.
- NCIT_C118697 normalizedInformationContent "100" @default.
- NCIT_C118697 referenceCount "1" @default.
- NCIT_C118697 hasExactSynonym "Hypochondroplasia" @default.
- NCIT_C118697 inSubset NCIT_C118467 @default.
- NCIT_C118697 inSubset NCIT_C165258 @default.
- NCIT_C118697 inSubset NCIT_C192842 @default.
- NCIT_C118697 inSubset NCIT_C90259 @default.
- NCIT_C118697 type Class @default.
- NCIT_C118697 isDefinedBy ncit.owl @default.
- NCIT_C118697 label "Hypochondroplasia" @default.
- NCIT_C118697 subClassOf NCIT_C118697 @default.
- NCIT_C118697 subClassOf NCIT_C2991 @default.
- NCIT_C118697 subClassOf NCIT_C4873 @default.
- NCIT_C118697 subClassOf NCIT_C53529 @default.
- NCIT_C118697 subClassOf NCIT_C53543 @default.
- NCIT_C118697 subClassOf NCIT_C53547 @default.
- NCIT_C118697 subClassOf NCIT_C7057 @default.
- NCIT_C118697 subClassOf NCIT_C84978 @default.