| Approved symbol | CTSA |
|---|---|
| Approved name | cathepsin A |
| HGCN ID | HGNC:9251 |
| Previous symbols | GSL, PPGB |
| Inheritance | |
| OMIM | 613111 |
| Chromosome | 20q13.12 |
| Panel(s) |
NGS Dementia/ALS NGS Intellectual disability NGS Mendeliome NGS Preconception panel (for consanguineous couples) NGS Skeletal Dysplasia NGS Treatable metabolic neurodegenerative disorders NGS White matter disease |
