Matches in Ubergraph for { <http://purl.obolibrary.org/obo/NCIT_C118786> ?p ?o ?g. }
Showing items 1 to 28 of
28
with 100 items per page.
- NCIT_C118786 IAO_0000115 "A rare, autosomal dominant inherited syndrome caused by mutations in the IRF6 gene. It is characterized by the presence of cleft palate, cleft lip, pits in the lower lip, web behind the knee (popliteal pterygium), syndactyly, cryptorchidism, scrotal malformation, and hypoplasia of the labia majora." @default.
- NCIT_C118786 NCIT_NHC0 "C118786" @default.
- NCIT_C118786 NCIT_P106 "Disease or Syndrome" @default.
- NCIT_C118786 NCIT_P108 "Autosomal Dominant Popliteal Pterygium Syndrome" @default.
- NCIT_C118786 NCIT_P207 "C0265259" @default.
- NCIT_C118786 NCIT_P322 "Cellosaurus" @default.
- NCIT_C118786 NCIT_R176 NCIT_C16612 @default.
- NCIT_C118786 NCIT_R176 NCIT_C20420 @default.
- NCIT_C118786 NCIT_R176 NCIT_C54362 @default.
- NCIT_C118786 NCIT_R176 NCIT_C75616 @default.
- NCIT_C118786 normalizedInformationContent "100" @default.
- NCIT_C118786 referenceCount "1" @default.
- NCIT_C118786 hasExactSynonym "Autosomal Dominant Popliteal Pterygium Syndrome" @default.
- NCIT_C118786 inSubset NCIT_C165258 @default.
- NCIT_C118786 inSubset NCIT_C192842 @default.
- NCIT_C118786 type Class @default.
- NCIT_C118786 isDefinedBy ncit.owl @default.
- NCIT_C118786 label "Autosomal Dominant Popliteal Pterygium Syndrome" @default.
- NCIT_C118786 subClassOf Bac69d83d077cc751b52eb5a2e22f9e70 @default.
- NCIT_C118786 subClassOf Bdd7761031fc1b41497cf689f68f06e2e @default.
- NCIT_C118786 subClassOf NCIT_C118786 @default.
- NCIT_C118786 subClassOf NCIT_C28193 @default.
- NCIT_C118786 subClassOf NCIT_C2991 @default.
- NCIT_C118786 subClassOf NCIT_C4873 @default.
- NCIT_C118786 subClassOf NCIT_C53529 @default.
- NCIT_C118786 subClassOf NCIT_C53543 @default.
- NCIT_C118786 subClassOf NCIT_C53547 @default.
- NCIT_C118786 subClassOf NCIT_C7057 @default.