| Approved symbol | SAMHD1 |
|---|---|
| Approved name | SAM and HD domain containing deoxynucleoside triphosphate triphosphohydrolase 1 |
| HGCN ID | HGNC:15925 |
| Previous symbols | |
| Inheritance | |
| OMIM | 606754 |
| Chromosome | 20q11.23 |
| Panel(s) |
NGS Dementia/ALS NGS Epilepsy NGS Intellectual disability NGS Mendeliome NGS Movement disorders NGS Preconception panel (for consanguineous couples) NGS Primary immunodeficiency PID NGS White matter disease SAMHD1 Analysis |
