PedAM
Pediatric Disease Annotations & Medicines
| Disease | microphthalmia |
| Phenotype | C1853235|sclerocornea |
| Sentences | 1 |
| PubMedID- 20664696 | Mutations in foxe3 cause recessive sclerocornea in association with microphthalmia, bilateral aphakia, absence of the iris and retinal dysplasia (omim 610256) [5-7]. |
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