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- Bbb34a22eceb4b9956e306caf7be2c6ad hasDbXref "NCIT:C132224" @default.
- Bbb34a22eceb4b9956e306caf7be2c6ad type Axiom @default.
- Bbb34a22eceb4b9956e306caf7be2c6ad annotatedProperty IAO_0000115 @default.
- Bbb34a22eceb4b9956e306caf7be2c6ad annotatedSource MONDO_0011457 @default.
- Bbb34a22eceb4b9956e306caf7be2c6ad annotatedTarget "An autosomal recessive condition caused by mutation(s) in the MRE11A gene, encoding double-strand break repair protein MRE11. It is characterized by progressive cerebellar degeneration resulting in ataxia and oculomotor apraxia." @default.