Glycine transporter 2 deficiency

Synonym(s)
- Hereditary hyperekplexia type 3
Type

Disease
External link(s)
- IEMbase
Gene
- SLC6A5 / Solute Carrier Family 6 Member 5
  11p15.1
  OMIM
  GnomAD
  Ensembl
  HGNC
  VMH
  LOVD
Gene product
- Glycine transporter 2
Disease group(s)
- 23.4 Glycine neurotransmitter disorders