| Approved symbol | CFH |
|---|---|
| Approved name | complement factor H |
| HGCN ID | HGNC:4883 |
| Previous symbols | HF, HF1, HF2 |
| Inheritance | |
| OMIM | 134370 |
| Chromosome | 1q31.3 |
| Panel(s) |
NGS Cone-rod dystrophy and macula degeneration NGS Leber’s congenital amaurosis LCA NGS Mendeliome NGS Preconception panel (for consanguineous couples) NGS Primary immunodeficiency PID NGS Retinitis pigmentosa NGS Vision disorder CSNB |
