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- NCIT_C175706 IAO_0000115 "A rare condition in which the two arms of chromosome 18 are fused resulting in a ring chromosome. Ring chromosome syndromes typically are characterized by developmental delay, intellectual disability, microcephaly, and dysmorphic facial features." @default.
- NCIT_C175706 NCIT_NHC0 "C175706" @default.
- NCIT_C175706 NCIT_P106 "Disease or Syndrome" @default.
- NCIT_C175706 NCIT_P108 "Ring Chromosome 18 Syndrome" @default.
- NCIT_C175706 NCIT_P208 "CL979353" @default.
- NCIT_C175706 NCIT_P322 "Cellosaurus" @default.
- NCIT_C175706 NCIT_R174 NCIT_C12219 @default.
- NCIT_C175706 NCIT_R174 NCIT_C13202 @default.
- NCIT_C175706 NCIT_R174 NCIT_C13203 @default.
- NCIT_C175706 NCIT_R174 NCIT_C13213 @default.
- NCIT_C175706 NCIT_R174 NCIT_C13404 @default.
- NCIT_C175706 NCIT_R174 NCIT_C14134 @default.
- NCIT_C175706 NCIT_R174 NCIT_C21599 @default.
- NCIT_C175706 normalizedInformationContent "100" @default.
- NCIT_C175706 referenceCount "1" @default.
- NCIT_C175706 hasExactSynonym "Ring Chromosome 18 Syndrome" @default.
- NCIT_C175706 inSubset NCIT_C165258 @default.
- NCIT_C175706 inSubset NCIT_C192842 @default.
- NCIT_C175706 type Class @default.
- NCIT_C175706 isDefinedBy ncit.owl @default.
- NCIT_C175706 label "Ring Chromosome 18 Syndrome" @default.
- NCIT_C175706 subClassOf B11017bd81ac1167e7703e54280f6f8c4 @default.
- NCIT_C175706 subClassOf Bef5beddddf2a81d5f99213d0d6e85149 @default.
- NCIT_C175706 subClassOf NCIT_C175706 @default.
- NCIT_C175706 subClassOf NCIT_C28193 @default.
- NCIT_C175706 subClassOf NCIT_C2991 @default.
- NCIT_C175706 subClassOf NCIT_C7057 @default.