| 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 Bewegingsstoornissen NGS Dementie NGS Epilepsie NGS Intellectual disability NGS Mendelioom NGS Preconceptiepanel (t.b.v. consanguine paren) NGS Primaire immunodeficientie PID NGS Wittestofziekten SAMHD1 Analysis |
