| 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 dystrophie en macula degeneratie NGS Leber congenital amaurosis LCA NGS Mendelioom NGS Preconceptiepanel (t.b.v. consanguine paren) NGS Primaire immunodeficientie PID NGS Retinitis pigmentosa NGS Visus pakket Retinale genen |
