Approved symbol | CTSD |
---|---|
Approved name | cathepsin D |
HGCN ID | HGNC:2529 |
Previous symbols | CPSD |
Inheritance | |
OMIM | 116840 |
Chromosome | 11p15.5 |
Panel(s) |
NGS Dementia/ALS NGS Epilepsy NGS Intellectual disability NGS Mendeliome NGS Preconception panel (for consanguineous couples) NGS Treatable metabolic neurodegenerative disorders |