Matches in Ubergraph for { <http://purl.obolibrary.org/obo/NCIT_C61252> ?p ?o ?g. }
Showing items 1 to 47 of
47
with 100 items per page.
- NCIT_C61252 IAO_0000115 "A rare metabolic disorder characterized by damage of the myelin sheaths in the nervous system and degeneration of the adrenal glands. It leads to progressive neurologic disorders, adrenal insufficiency and death." @default.
- NCIT_C61252 NCIT_NHC0 "C61252" @default.
- NCIT_C61252 NCIT_P106 "Disease or Syndrome" @default.
- NCIT_C61252 NCIT_P107 "Adrenoleukodystrophy" @default.
- NCIT_C61252 NCIT_P108 "Adrenoleukodystrophy" @default.
- NCIT_C61252 NCIT_P207 "C0162309" @default.
- NCIT_C61252 NCIT_P322 "CTRP" @default.
- NCIT_C61252 NCIT_P322 "Cellosaurus" @default.
- NCIT_C61252 NCIT_P322 "NICHD" @default.
- NCIT_C61252 NCIT_P325 "An X-linked recessive condition caused by mutation(s) in the ABCD1 gene, resulting in defective peroxisomal fatty acid oxidation and accumulation of saturated very long chain fatty acids in all tissues of the body. Clinical manifestations of the condition vary in severity, and can include progressive loss of adrenal gland function, Leydig cell dysfunction, and neurodegenerative changes." @default.
- NCIT_C61252 NCIT_P366 "Adrenoleukodystrophy" @default.
- NCIT_C61252 NCIT_R100 NCIT_C12219 @default.
- NCIT_C61252 NCIT_R100 NCIT_C12755 @default.
- NCIT_C61252 NCIT_R100 NCIT_C12919 @default.
- NCIT_C61252 NCIT_R176 NCIT_C142193 @default.
- NCIT_C61252 NCIT_R176 NCIT_C158414 @default.
- NCIT_C61252 NCIT_R176 NCIT_C16612 @default.
- NCIT_C61252 NCIT_R176 NCIT_C21281 @default.
- NCIT_C61252 NCIT_R176 NCIT_C21295 @default.
- NCIT_C61252 NCIT_R176 NCIT_C28533 @default.
- NCIT_C61252 normalizedInformationContent "90.826665450122817" @default.
- NCIT_C61252 referenceCount "4" @default.
- NCIT_C61252 hasExactSynonym "Adrenoleukodystrophy" @default.
- NCIT_C61252 hasExactSynonym "Schilder Disease" @default.
- NCIT_C61252 inSubset NCIT_C116977 @default.
- NCIT_C61252 inSubset NCIT_C118168 @default.
- NCIT_C61252 inSubset NCIT_C118467 @default.
- NCIT_C61252 inSubset NCIT_C165258 @default.
- NCIT_C61252 inSubset NCIT_C192842 @default.
- NCIT_C61252 inSubset NCIT_C90259 @default.
- NCIT_C61252 type Class @default.
- NCIT_C61252 isDefinedBy ncit.owl @default.
- NCIT_C61252 label "Adrenoleukodystrophy" @default.
- NCIT_C61252 subClassOf B39efd28df4280924d07ee83054bd55c0 @default.
- NCIT_C61252 subClassOf Be394b37d8b65863e0896c85ff936c440 @default.
- NCIT_C61252 subClassOf NCIT_C26835 @default.
- NCIT_C61252 subClassOf NCIT_C27551 @default.
- NCIT_C61252 subClassOf NCIT_C27588 @default.
- NCIT_C61252 subClassOf NCIT_C2991 @default.
- NCIT_C61252 subClassOf NCIT_C4873 @default.
- NCIT_C61252 subClassOf NCIT_C53529 @default.
- NCIT_C61252 subClassOf NCIT_C53531 @default.
- NCIT_C61252 subClassOf NCIT_C53543 @default.
- NCIT_C61252 subClassOf NCIT_C53547 @default.
- NCIT_C61252 subClassOf NCIT_C61252 @default.
- NCIT_C61252 subClassOf NCIT_C61253 @default.
- NCIT_C61252 subClassOf NCIT_C7057 @default.