| Approved symbol | IMPDH1 |
|---|---|
| Approved name | inosine monophosphate dehydrogenase 1 |
| HGCN ID | HGNC:6052 |
| Previous symbols | RP10 |
| Inheritance | |
| OMIM | 146690 |
| Chromosome | 7q32.1 |
| Panel(s) |
NGS Cone-rod dystrophy and macula degeneration NGS Leber’s congenital amaurosis LCA NGS Mendeliome NGS Retinitis pigmentosa NGS Treatable metabolic neurodegenerative disorders NGS Vision disorder CSNB |
