Matches in Ubergraph for { <https://frink.apps.renci.org/.well-known/genid/B90b5d1ccfa5df04ddc86cfa37959f6a8> ?p ?o ?g. }
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- B90b5d1ccfa5df04ddc86cfa37959f6a8 hasDbXref "MESH:D017094" @default.
- B90b5d1ccfa5df04ddc86cfa37959f6a8 type Axiom @default.
- B90b5d1ccfa5df04ddc86cfa37959f6a8 annotatedProperty IAO_0000115 @default.
- B90b5d1ccfa5df04ddc86cfa37959f6a8 annotatedSource MONDO_0002520 @default.
- B90b5d1ccfa5df04ddc86cfa37959f6a8 annotatedTarget "A group of metabolic diseases due to deficiency of one of a number of liver enzymes in the biosynthetic pathway of heme. They are characterized by the accumulation and increased excretion of porphyrins or its precursors. Clinical features include neurological symptoms (porphyria, acute intermittent), cutaneous lesions due to photosensitivity (porphyria cutanea tarda), or both (hereditary coproporphyria). Hepatic porphyrias can be hereditary or acquired as a result of toxicity to the hepatic tissues." @default.