eRAM
encyclopedia of Rare Disease Annotation for Precision Medicine
| Disease | retinal degeneration |
| Comorbidity | C0029124|optic nerve atrophy |
| Sentences | 1 |
| PubMedID- 21423525 | Mutations in opa1 cause autosomal dominant optic atrophy (doa), characterized by a degeneration of retinal ganglia cells leading to optic nerve atrophy (alexander et al., 2000; delettre et al., 2000). |
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