KCND3

potassium voltage-gated channel subfamily D member 3
OMIM: 605411
PanelMode of inheritanceDetails
4 panels
R-numbers: R58
Signed-off version 5.0
MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Phenotypes
Spinocerebellarataxia19, OMIM:607346
Component of the following Super Panels:
  • - Hereditary ataxia and cerebellar anomalies - childhood onset
Signed-off version 5.0
MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Phenotypes
Spinocerebellarataxia19,607346
Green
in DDG2P
Component of the following Super Panels:
  • - Paediatric disorders
Signed-off version 4.0
MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Phenotypes
KCND3-related developmental disorder (monoallelic)
R-numbers: R54
Signed-off version 5.0
MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Phenotypes
Spinocerebellar ataxia 19, 607346, Spinocerebellarataxia19, 607346