SLC35A2-CDG

Synonym(s)
- Early infantile epileptic encephalopathy 22
Type

Disease
External link(s)
- Orphanet
- IEMbase
Gene
- SLC35A2 / solute carrier family 35 member A2
  Xp11.23
  OMIM
  GnomAD
  Ensembl
  HGNC
  VMH
  LOVD
Gene product
- UDP-galactose transporter
Disease group(s)
- 18.4.2 Disorders of Golgi transport
Child entries
- Isolated focal cortical dysplasia type Ia