PedAM
Pediatric Disease Annotations & Medicines
| Disease | retinal detachment |
| Symptom | C0344290|vitreoretinal degeneration |
| Sentences | 1 |
| PubMedID- 21163348 | Mutations in the collagen xviii gene lead to the knobloch syndrome, which is characterized by high myopia, vitreoretinal degeneration with retinal detachment, macular abnormalities and occipital encephalocele. |
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