PedAM
Pediatric Disease Annotations & Medicines
| Disease | eye disease |
| Phenotype | C0035334|retinitis pigmentosa |
| Sentences | 2 |
| PubMedID- 21655914 | A hereditary eye disease, x-linked retinitis pigmentosa, is linked to mutations in the n-terminal domain of the rp2 gene that shares amino acid sequence similarity with the tbcc [54, 55]. |
| PubMedID- 25241976 | Conclusions: retinitis pigmentosa is a kind of genetic eye disease with diversity clinical phenotypes. |
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