eRAM
encyclopedia of Rare Disease Annotation for Precision Medicine
| Disease | optic atrophy 1 |
| Comorbidity | C0030486|paraplegia |
| Sentences | 2 |
| PubMedID- 26281626 | Reply: spastic paraplegia in 'dominant optic atrophy plus' phenotype due to opa1 mutation. |
| PubMedID- 21646330 | Spastic paraplegia in 'dominant optic atrophy plus' phenotype due to opa1 mutation. |
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