| Approved symbol | FA2H |
|---|---|
| Approved name | fatty acid 2-hydroxylase |
| HGCN ID | HGNC:21197 |
| Previous symbols | FAXDC1, SPG35 |
| Inheritance | |
| OMIM | 611026 |
| Chromosome | 16q23.1 |
| Panel(s) |
FA2H Analysis NGS Dementia/ALS NGS Epilepsy NGS Intellectual disability NGS Mendeliome NGS Movement disorders NGS Neurodegeneration with brain iron accumulation NBIA NGS Preconception panel (for consanguineous couples) NGS Treatable metabolic neurodegenerative disorders |
