PedAM
Pediatric Disease Annotations & Medicines
| Disease | cataract |
| Symptom | C0029124|optic atrophy |
| Sentences | 2 |
| PubMedID- 22392506 | Heterozygous opa3 mutations were subsequently reported in two french families with a dominantly inherited form of optic atrophy associated with premature cataract formation (adoac) . |
| PubMedID- 23401657 | Opa3 mutations result in optic atrophy associated with cataract , while tmem126a mutations are responsible for an autosomal recessive form of optic atrophy . |
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