| Approved symbol | C19orf12 |
|---|---|
| Approved name | chromosome 19 open reading frame 12 |
| HGCN ID | HGNC:25443 |
| Previous symbols | SPG43 |
| Inheritance | |
| OMIM | 614297 |
| Chromosome | 19q12 |
| Panel(s) |
NGS Dementia/ALS NGS Mendeliome NGS Movement disorders NGS Neurodegeneration with brain iron accumulation NBIA NGS Optic atrophy NGS Parkinson NGS Preconception panel (for consanguineous couples) |
