PedAM
Pediatric Disease Annotations & Medicines
| Disease | mitochondrial disorders |
| Phenotype | C0456909|vision loss |
| Sentences | 1 |
| PubMedID- 22400981 | Leber hereditary optic neuropathy (lhon, mim535000) is one of the most common mitochondrial disorders, which mainly leads to vision loss in young males [1-3]. |
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