Approved symbol | CTSD |
---|---|
Approved name | cathepsin D |
HGCN ID | HGNC:2529 |
Previous symbols | CPSD |
Inheritance | |
OMIM | 116840 |
Chromosome | 11p15.5 |
Panel(s) |
NGS Dementie NGS Epilepsie NGS Intellectual disability NGS Mendelioom NGS Metabole aandoeningen NGS Preconceptiepanel (t.b.v. consanguine paren) |