Tyrosine hydroxylase deficiency

Type

Disease
External link(s)
- IEMbase
Gene
- TH / Tyrosine Hydroxylase
  11p15.5
  OMIM
  GnomAD
  Ensembl
  HGNC
  VMH
  LOVD
Gene product
- Tyrosine 3-monooxygenase
Disease group(s)
- 23.1 Monoamine neurotransmission
Child entries
- TH-related dopa-responsive dystonia