Matches in Ubergraph for { <http://purl.obolibrary.org/obo/NCIT_C84908> ?p ?o ?g. }
Showing items 1 to 30 of
30
with 100 items per page.
- NCIT_C84908 IAO_0000115 "A rare autosomal recessive lysosomal storage disease caused by mutations in SUMF1 gene. It is characterized by deficiency of all sulfatase enzymes. Signs and symptoms include neurologic damage, mental retardation, skeletal abnormalities, hepatosplenomegaly, and ichthyosis." @default.
- NCIT_C84908 NCIT_NHC0 "C84908" @default.
- NCIT_C84908 NCIT_P106 "Disease or Syndrome" @default.
- NCIT_C84908 NCIT_P108 "Multiple Sulfatase Deficiency Disease" @default.
- NCIT_C84908 NCIT_P207 "C0268263" @default.
- NCIT_C84908 NCIT_P322 "Cellosaurus" @default.
- NCIT_C84908 NCIT_R176 NCIT_C127891 @default.
- NCIT_C84908 NCIT_R176 NCIT_C16612 @default.
- NCIT_C84908 NCIT_R176 NCIT_C21281 @default.
- NCIT_C84908 NCIT_R176 NCIT_C25939 @default.
- NCIT_C84908 normalizedInformationContent "100" @default.
- NCIT_C84908 referenceCount "1" @default.
- NCIT_C84908 hasExactSynonym "Multiple Sulfatase Deficiency Disease" @default.
- NCIT_C84908 inSubset NCIT_C165258 @default.
- NCIT_C84908 inSubset NCIT_C192842 @default.
- NCIT_C84908 type Class @default.
- NCIT_C84908 isDefinedBy ncit.owl @default.
- NCIT_C84908 label "Multiple Sulfatase Deficiency Disease" @default.
- NCIT_C84908 subClassOf B640777ee0b0ce99ba65bc2fe018d7313 @default.
- NCIT_C84908 subClassOf B651dac9daa26b2898c440be6bb9fcceb @default.
- NCIT_C84908 subClassOf NCIT_C2991 @default.
- NCIT_C84908 subClassOf NCIT_C3235 @default.
- NCIT_C84908 subClassOf NCIT_C34816 @default.
- NCIT_C84908 subClassOf NCIT_C4873 @default.
- NCIT_C84908 subClassOf NCIT_C53529 @default.
- NCIT_C84908 subClassOf NCIT_C53543 @default.
- NCIT_C84908 subClassOf NCIT_C53547 @default.
- NCIT_C84908 subClassOf NCIT_C61250 @default.
- NCIT_C84908 subClassOf NCIT_C7057 @default.
- NCIT_C84908 subClassOf NCIT_C84908 @default.