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- B4aab0e69b43ab1089fa073628cd1792d NCIT_P378 "NICHD" @default.
- B4aab0e69b43ab1089fa073628cd1792d type Axiom @default.
- B4aab0e69b43ab1089fa073628cd1792d annotatedProperty NCIT_P325 @default.
- B4aab0e69b43ab1089fa073628cd1792d annotatedSource NCIT_C61252 @default.
- B4aab0e69b43ab1089fa073628cd1792d annotatedTarget "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.