CLN14 disease

Synonym(s)
- Progressive myoclonic epilepsy type 3
Type

Disease
External link(s)
- Orphanet
- IEMbase
Gene
- KCTD7 / Potassium Channel Tetramerization Domain Containing 7
  7q11.21
  OMIM
  GnomAD
  Ensembl
  HGNC
  VMH
  LOVD
Gene product
- Potassium channel tetramerization domain-containing protein 7
Disease group(s)
- 20.4 Neuronal ceroid lipofuscinoses (NCL)