Matches in Ubergraph for { <http://purl.obolibrary.org/obo/NCIT_C84698> ?p ?o ?g. }
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- NCIT_C84698 IAO_0000115 "A rare congenital metabolic disorder characterized by an inborn error of porphyrin-heme biosynthesis. It is caused by deficiency of the enzyme ferrochelatase. Signs and symptoms include painful cutaneous photosensitivity leading to blistering and scarring of the exposed skin areas, erythrodontia, red discoloration of urine, hemolytic anemia, and splenomegaly." @default.
- NCIT_C84698 NCIT_NHC0 "C84698" @default.
- NCIT_C84698 NCIT_P106 "Disease or Syndrome" @default.
- NCIT_C84698 NCIT_P108 "Erythropoietic Protoporphyria" @default.
- NCIT_C84698 NCIT_P207 "C0162568" @default.
- NCIT_C84698 NCIT_P322 "Cellosaurus" @default.
- NCIT_C84698 normalizedInformationContent "100" @default.
- NCIT_C84698 referenceCount "1" @default.
- NCIT_C84698 hasExactSynonym "EPP" @default.
- NCIT_C84698 hasExactSynonym "Erythropoietic Protoporphyria" @default.
- NCIT_C84698 hasExactSynonym "Protoporphyria, Erythropoietic" @default.
- NCIT_C84698 inSubset NCIT_C165258 @default.
- NCIT_C84698 inSubset NCIT_C192842 @default.
- NCIT_C84698 type Class @default.
- NCIT_C84698 isDefinedBy ncit.owl @default.
- NCIT_C84698 label "Erythropoietic Protoporphyria" @default.
- NCIT_C84698 subClassOf NCIT_C2991 @default.
- NCIT_C84698 subClassOf NCIT_C3235 @default.
- NCIT_C84698 subClassOf NCIT_C4873 @default.
- NCIT_C84698 subClassOf NCIT_C53529 @default.
- NCIT_C84698 subClassOf NCIT_C53543 @default.
- NCIT_C84698 subClassOf NCIT_C53547 @default.
- NCIT_C84698 subClassOf NCIT_C7057 @default.
- NCIT_C84698 subClassOf NCIT_C84698 @default.
- NCIT_C84698 subClassOf NCIT_C97096 @default.