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- NCIT_C126813 IAO_0000115 "An autosomal recessive condition due to mutation(s) in the CYP11B2 gene that results in decreased activity of mitochondrial cytochrome P450 11B2 with reduced aldosterone synthesis and salt wasting." @default.
- NCIT_C126813 NCIT_A13 NCIT_C40062 @default.
- NCIT_C126813 NCIT_NHC0 "C126813" @default.
- NCIT_C126813 NCIT_P106 "Finding" @default.
- NCIT_C126813 NCIT_P108 "Aldosterone Synthase Deficiency" @default.
- NCIT_C126813 NCIT_P207 "C0268293" @default.
- NCIT_C126813 NCIT_P322 "NICHD" @default.
- NCIT_C126813 NCIT_P325 "An autosomal recessive condition due to mutation(s) in the CYP11B2 gene that results in decreased activity of mitochondrial cytochrome P450 11B2 with reduced aldosterone synthesis and salt wasting." @default.
- NCIT_C126813 normalizedInformationContent "92.730304365937428" @default.
- NCIT_C126813 referenceCount "3" @default.
- NCIT_C126813 hasExactSynonym "Aldosterone Synthase Deficiency" @default.
- NCIT_C126813 hasExactSynonym "Corticosterone Methyl Oxidase Deficiency" @default.
- NCIT_C126813 inSubset NCIT_C118467 @default.
- NCIT_C126813 inSubset NCIT_C90259 @default.
- NCIT_C126813 type Class @default.
- NCIT_C126813 isDefinedBy ncit.owl @default.
- NCIT_C126813 label "Aldosterone Synthase Deficiency" @default.
- NCIT_C126813 subClassOf NCIT_C113206 @default.
- NCIT_C126813 subClassOf NCIT_C126813 @default.
- NCIT_C126813 subClassOf NCIT_C3367 @default.
- NCIT_C126813 subClassOf NCIT_C36278 @default.
- NCIT_C126813 subClassOf NCIT_C36285 @default.
- NCIT_C126813 subClassOf NCIT_C7057 @default.
- NCIT_C126813 subClassOf NCIT_C92809 @default.