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- NCIT_C99104 IAO_0000115 "An inherited metabolic disorder characterized by increased levels of galactose in the blood. Clinical signs include failure to thrive, developmental delays, liver damage and jaundice, cataract, and ovarian failure." @default.
- NCIT_C99104 NCIT_A13 NCIT_C148332 @default.
- NCIT_C99104 NCIT_NHC0 "C99104" @default.
- NCIT_C99104 NCIT_P106 "Disease or Syndrome" @default.
- NCIT_C99104 NCIT_P108 "UTP-Hexose-1-Phosphate Uridylyltransferase Deficiency" @default.
- NCIT_C99104 NCIT_P208 "CL432934" @default.
- NCIT_C99104 NCIT_P322 "NICHD" @default.
- NCIT_C99104 normalizedInformationContent "100" @default.
- NCIT_C99104 referenceCount "1" @default.
- NCIT_C99104 hasExactSynonym "UTP-Hexose-1-Phosphate Uridylyltransferase Deficiency" @default.
- NCIT_C99104 inSubset NCIT_C90259 @default.
- NCIT_C99104 inSubset NCIT_C99147 @default.
- NCIT_C99104 type Class @default.
- NCIT_C99104 isDefinedBy ncit.owl @default.
- NCIT_C99104 label "UTP-Hexose-1-Phosphate Uridylyltransferase Deficiency" @default.
- NCIT_C99104 subClassOf NCIT_C2991 @default.
- NCIT_C99104 subClassOf NCIT_C3235 @default.
- NCIT_C99104 subClassOf NCIT_C34816 @default.
- NCIT_C99104 subClassOf NCIT_C53529 @default.
- NCIT_C99104 subClassOf NCIT_C53547 @default.
- NCIT_C99104 subClassOf NCIT_C7057 @default.
- NCIT_C99104 subClassOf NCIT_C84723 @default.
- NCIT_C99104 subClassOf NCIT_C97089 @default.
- NCIT_C99104 subClassOf NCIT_C99104 @default.