PedAM
Pediatric Disease Annotations & Medicines
| Disease | auditory neuropathy |
| Phenotype | C0029124|optic atrophy |
| Sentences | 1 |
| PubMedID- 22815638 | In another algerian family, affected patients bearing the homozygous p.arg55x mutation in tmem126a presented with optic atrophy associated with auditory neuropathy [6]. |
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