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- NCIT_C131451 IAO_0000115 "A variant of familial glucocorticoid deficiency caused by a defect in the steroidogenic acute regulatory protein; it may mimic lipoid congenital adrenal hyperplasia." @default.
- NCIT_C131451 NCIT_NHC0 "C131451" @default.
- NCIT_C131451 NCIT_P106 "Finding" @default.
- NCIT_C131451 NCIT_P108 "Familial Glucocorticoid Deficiency Type 3" @default.
- NCIT_C131451 NCIT_P207 "C1836621" @default.
- NCIT_C131451 NCIT_P322 "NICHD" @default.
- NCIT_C131451 NCIT_P325 "A variant of familial glucocorticoid deficiency caused by a defect in the steroidogenic acute regulatory protein; it may mimic lipoid congenital adrenal hyperplasia." @default.
- NCIT_C131451 normalizedInformationContent "100" @default.
- NCIT_C131451 referenceCount "1" @default.
- NCIT_C131451 hasExactSynonym "Familial Glucocorticoid Deficiency Type 3" @default.
- NCIT_C131451 hasExactSynonym "GCCD3" @default.
- NCIT_C131451 hasExactSynonym "Non-classic CLAH (FGD variant)" @default.
- NCIT_C131451 inSubset NCIT_C118467 @default.
- NCIT_C131451 inSubset NCIT_C90259 @default.
- NCIT_C131451 type Class @default.
- NCIT_C131451 isDefinedBy ncit.owl @default.
- NCIT_C131451 label "Familial Glucocorticoid Deficiency Type 3" @default.
- NCIT_C131451 subClassOf NCIT_C120446 @default.
- NCIT_C131451 subClassOf NCIT_C131451 @default.
- NCIT_C131451 subClassOf NCIT_C3367 @default.
- NCIT_C131451 subClassOf NCIT_C36278 @default.
- NCIT_C131451 subClassOf NCIT_C36285 @default.
- NCIT_C131451 subClassOf NCIT_C7057 @default.
- NCIT_C131451 subClassOf NCIT_C92809 @default.