| Approved symbol | CTSA |
|---|---|
| Approved name | cathepsin A |
| HGCN ID | HGNC:9251 |
| Previous symbols | GSL, PPGB |
| Inheritance | |
| OMIM | 613111 |
| Chromosome | 20q13.12 |
| Panel(s) |
NGS Dementie NGS Intellectual disability NGS Mendelioom NGS Metabole aandoeningen NGS Preconceptiepanel (t.b.v. consanguine paren) NGS Skeletdysplasie NGS Wittestofziekten |
