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- B5acd90b4f9d1699ccc2906505f9996ad NCIT_P378 "NCI" @default.
- B5acd90b4f9d1699ccc2906505f9996ad type Axiom @default.
- B5acd90b4f9d1699ccc2906505f9996ad annotatedProperty IAO_0000115 @default.
- B5acd90b4f9d1699ccc2906505f9996ad annotatedSource NCIT_C186789 @default.
- B5acd90b4f9d1699ccc2906505f9996ad annotatedTarget "An autosomal recessive disorder caused by mutation(s) in the ADAT3 gene, encoding probable inactive tRNA-specific adenosine deaminase-like protein 3. It is characterized by a neurodevelopmental disorder with brain abnormalities, poor growth, and abnormal facies." @default.