Matches in Ubergraph for { <http://purl.obolibrary.org/obo/NCIT_C61271> ?p ?o ?g. }
Showing items 1 to 43 of
43
with 100 items per page.
- NCIT_C61271 IAO_0000115 "A very rare, autosomal recessive inherited lysosomal storage disease caused by mutations in the LIPA gene. Signs and symptoms appear in infancy and include developmental delay, vomiting, abdominal distention, hepatosplenomegaly, jaundice, anemia, steatorrhea, and calcification of the adrenal glands." @default.
- NCIT_C61271 NCIT_NHC0 "C61271" @default.
- NCIT_C61271 NCIT_P106 "Disease or Syndrome" @default.
- NCIT_C61271 NCIT_P107 "Wolman Disease" @default.
- NCIT_C61271 NCIT_P108 "Wolman Disease" @default.
- NCIT_C61271 NCIT_P207 "C0043208" @default.
- NCIT_C61271 NCIT_P322 "CTRP" @default.
- NCIT_C61271 NCIT_P322 "Cellosaurus" @default.
- NCIT_C61271 NCIT_P322 "NICHD" @default.
- NCIT_C61271 NCIT_P325 "An autosomal recessive condition caused by mutation(s) in the LIPA gene, resulting in lysosomal acid lipase deficiency, which leads to accumulation of cholesterol esters and triglycerides in many organs." @default.
- NCIT_C61271 NCIT_P366 "Wolman_Disease" @default.
- NCIT_C61271 NCIT_R176 NCIT_C16612 @default.
- NCIT_C61271 NCIT_R176 NCIT_C188895 @default.
- NCIT_C61271 NCIT_R176 NCIT_C21281 @default.
- NCIT_C61271 NCIT_R176 NCIT_C25804 @default.
- NCIT_C61271 NCIT_R176 NCIT_C25952 @default.
- NCIT_C61271 normalizedInformationContent "100" @default.
- NCIT_C61271 referenceCount "1" @default.
- NCIT_C61271 hasExactSynonym "Lysosomal Acid Lipase Deficiency" @default.
- NCIT_C61271 hasExactSynonym "Wolman Disease" @default.
- NCIT_C61271 hasExactSynonym "Wolman's Disease" @default.
- NCIT_C61271 inSubset NCIT_C116977 @default.
- NCIT_C61271 inSubset NCIT_C118168 @default.
- NCIT_C61271 inSubset NCIT_C118467 @default.
- NCIT_C61271 inSubset NCIT_C165258 @default.
- NCIT_C61271 inSubset NCIT_C192842 @default.
- NCIT_C61271 inSubset NCIT_C90259 @default.
- NCIT_C61271 inSubset NCIT_C99147 @default.
- NCIT_C61271 type Class @default.
- NCIT_C61271 isDefinedBy ncit.owl @default.
- NCIT_C61271 label "Wolman Disease" @default.
- NCIT_C61271 subClassOf B91104a825f329d0fd6da50d7de7e24e5 @default.
- NCIT_C61271 subClassOf B952b692beea3e80c199eba28a3381594 @default.
- NCIT_C61271 subClassOf NCIT_C2991 @default.
- NCIT_C61271 subClassOf NCIT_C3235 @default.
- NCIT_C61271 subClassOf NCIT_C34816 @default.
- NCIT_C61271 subClassOf NCIT_C4873 @default.
- NCIT_C61271 subClassOf NCIT_C53529 @default.
- NCIT_C61271 subClassOf NCIT_C53543 @default.
- NCIT_C61271 subClassOf NCIT_C53547 @default.
- NCIT_C61271 subClassOf NCIT_C61250 @default.
- NCIT_C61271 subClassOf NCIT_C61271 @default.
- NCIT_C61271 subClassOf NCIT_C7057 @default.