| Approved symbol | PHYH |
|---|---|
| Approved name | phytanoyl-CoA 2-hydroxylase |
| HGCN ID | HGNC:8940 |
| Previous symbols | |
| Inheritance | |
| OMIM | 602026 |
| Chromosome | 10p13 |
| Panel(s) |
NGS Bewegingsstoornissen NGS Cone-rod dystrophie en macula degeneratie NGS Leber congenital amaurosis LCA NGS Mendelioom NGS Metabole aandoeningen NGS Neuropathy/Charcot Marie Tooth NGS Preconceptiepanel (t.b.v. consanguine paren) NGS Retinitis pigmentosa NGS Visus pakket Retinale genen NGS Wittestofziekten |
