ATXN2_CAG

PanelMode of inheritanceDetails
5 panels
R-numbers: R56
Signed-off version 3.12
MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Phenotypes
Spinocerebellar ataxia 2, OMIM:183090, {Amyotrophic lateral sclerosis, susceptibility to, 13}, OMIM:183090, {Parkinson disease, late-onset, susceptibility to}, OMIM:168600
R-numbers: R60
Signed-off version 4.0
MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Phenotypes
Spinocerebellar ataxia 2, OMIM:183090, {Amyotrophic lateral sclerosis, susceptibility to, 13}, OMIM:183090
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
Spinocerebellar ataxia 2, OMIM:183090
R-numbers: R57
Signed-off version 4.0
MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Phenotypes
Spinocerebellar ataxia 2, OMIM:183090, {Amyotrophic lateral sclerosis, susceptibility to, 13}, OMIM:183090
R-numbers: R54
Signed-off version 5.0
MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Phenotypes
Spinocerebellar ataxia 2, OMIM:183090