| Approved symbol | IFIH1 |
|---|---|
| Approved name | interferon induced with helicase C domain 1 |
| HGCN ID | HGNC:18873 |
| Previous symbols | |
| Inheritance | |
| OMIM | 606951 |
| Chromosome | 2q24.2 |
| Panel(s) |
IFIH1 Analysis NGS Dementia/ALS NGS Epilepsy NGS Intellectual disability NGS Mendeliome NGS Primary immunodeficiency PID NGS Skeletal Dysplasia NGS White matter disease |
