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- B208a1b78af804c9ac2052a4878e8dd60 NCIT_P378 "NCI" @default.
- B208a1b78af804c9ac2052a4878e8dd60 type Axiom @default.
- B208a1b78af804c9ac2052a4878e8dd60 annotatedProperty IAO_0000115 @default.
- B208a1b78af804c9ac2052a4878e8dd60 annotatedSource NCIT_C34842 @default.
- B208a1b78af804c9ac2052a4878e8dd60 annotatedTarget "A genetic syndrome usually inherited as an X-link trait. It is caused by abnormalities in the COL4A5 gene. It affects males more often than females and is characterized by hematuria, progressive renal insufficiency, hearing loss, and ocular abnormalities." @default.