eRAM
encyclopedia of Rare Disease Annotation for Precision Medicine
| Disease | retinal degeneration |
| Comorbidity | C0042790|visual disorder |
| Sentences | 1 |
| PubMedID- 26218912 | Purpose: mutations in the opa1 gene cause autosomal dominant optic atrophy (adoa), a visual disorder associated with degeneration of retinal ganglion cells (rgcs). |
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