| Approved symbol | UNC13D |
|---|---|
| Approved name | unc-13 homolog D |
| HGCN ID | HGNC:23147 |
| Previous symbols | |
| Inheritance | |
| OMIM | 608897 |
| Chromosome | 17q25.3 |
| Panel(s) |
NGS Hemophagocytic syndrome (HLH) NGS Mendeliome NGS Preconception panel (for consanguineous couples) NGS Primary immunodeficiency PID |
