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- NCIT_C84899 IAO_0000115 "A rare autosomal recessive lysosomal storage disease caused by deficiency of the enzyme acetyl-CoA:alpha-glucosaminide acetyltransferase. It is characterized by behavioral changes, sleep disturbances, and mental developmental delays." @default.
- NCIT_C84899 NCIT_NHC0 "C84899" @default.
- NCIT_C84899 NCIT_P106 "Disease or Syndrome" @default.
- NCIT_C84899 NCIT_P108 "Mucopolysaccharidosis Type IIIC" @default.
- NCIT_C84899 NCIT_P207 "C0086649" @default.
- NCIT_C84899 NCIT_P322 "Cellosaurus" @default.
- NCIT_C84899 normalizedInformationContent "100" @default.
- NCIT_C84899 referenceCount "1" @default.
- NCIT_C84899 hasExactSynonym "MPS III C" @default.
- NCIT_C84899 hasExactSynonym "Mucopolysaccharidosis Type IIIC" @default.
- NCIT_C84899 hasExactSynonym "Sanfilippo C" @default.
- NCIT_C84899 inSubset NCIT_C165258 @default.
- NCIT_C84899 inSubset NCIT_C192842 @default.
- NCIT_C84899 type Class @default.
- NCIT_C84899 isDefinedBy ncit.owl @default.
- NCIT_C84899 label "Mucopolysaccharidosis Type IIIC" @default.
- NCIT_C84899 subClassOf NCIT_C28193 @default.
- NCIT_C84899 subClassOf NCIT_C2991 @default.
- NCIT_C84899 subClassOf NCIT_C3235 @default.
- NCIT_C84899 subClassOf NCIT_C34816 @default.
- NCIT_C84899 subClassOf NCIT_C4873 @default.
- NCIT_C84899 subClassOf NCIT_C53529 @default.
- NCIT_C84899 subClassOf NCIT_C53543 @default.
- NCIT_C84899 subClassOf NCIT_C53547 @default.
- NCIT_C84899 subClassOf NCIT_C61250 @default.
- NCIT_C84899 subClassOf NCIT_C61259 @default.
- NCIT_C84899 subClassOf NCIT_C61262 @default.
- NCIT_C84899 subClassOf NCIT_C7057 @default.
- NCIT_C84899 subClassOf NCIT_C84899 @default.
- NCIT_C84899 subClassOf NCIT_C97089 @default.