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| DOID:0110377 | Name | retinitis pigmentosa 49 | |||
|---|---|---|---|---|---|
| Status | Valid | ||||
| Definition | A retinitis pigmentosa that has_material_basis_in mutation in the CNGA1 gene on chromosome 4p12. | ||||
| Synonym | Exact | RP49 | |||
| Parent | Is_a | DOID:10584 | |||
| DB_info | Database | OMIM | disease | 613756 | |
| Attribute_of | Gene_by_orthology | WBGene00000487 | |||
| WBGene00006526 | |||||
| WBGene00022295 |
