| Approved symbol | SPART |
|---|---|
| Approved name | spartin |
| HGCN ID | HGNC:18514 |
| Previous symbols | SPG20 |
| Inheritance | |
| OMIM | 607111 |
| Chromosome | 13q13.3 |
| Panel(s) |
NGS Bewegingsstoornissen NGS Intellectual disability NGS Mendelioom NGS Preconceptiepanel (t.b.v. consanguine paren) |
