KCTD17

potassium channel tetramerization domain containing 17
OMIM: 616386, Gene2Phenotype

1 panel

Panel Reviews Mode of inheritance Details
1 panel
Green KCTD17 in Childhood onset dystonia, chorea or related movement disorder


Version 3.77
Latest signed off version: v3.0 (22 Mar 2023)

review MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Sources
  • Expert Review Green
  • London North GLH
Phenotypes
  • Dystonia 26, myoclonic