| Approved symbol | TH |
|---|---|
| Approved name | tyrosine hydroxylase |
| HGCN ID | HGNC:11782 |
| Previous symbols | |
| Inheritance | |
| OMIM | 191290 |
| Chromosome | 11p15.5 |
| Panel(s) |
NGS Intellectual disability NGS Mendeliome NGS Movement disorders NGS Parkinson NGS Preconception panel (for consanguineous couples) NGS Treatable metabolic neurodegenerative disorders |
