Approved symbol | KLHL7 |
---|---|
Approved name | kelch like family member 7 |
HGCN ID | HGNC:15646 |
Previous symbols | |
Inheritance | |
OMIM | 611119 |
Chromosome | 7p15.3 |
Panel(s) |
NGS Cone-rod dystrophy and macula degeneration NGS Leber’s congenital amaurosis LCA NGS Mendeliome NGS Preconception panel (for consanguineous couples) NGS Retinitis pigmentosa NGS Vision disorder CSNB |