MRE11

MRE11 homolog, double strand break repair nuclease
OMIM: 600814
PanelMode of inheritanceDetails
4 panels
Component of the following Super Panels:
  • - Hereditary ataxia and cerebellar anomalies - childhood onset
Signed-off version 2.23
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Ataxia-telangiectasia-like disorder, Ataxia-Telangiectasia-Like Disorder
R-numbers: R57
Signed-off version 1.58
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Ataxia-telangiectasia-like disorder 1, 604391
Green
in DDG2P
Component of the following Super Panels:
  • - Paediatric disorders
Signed-off version 2.2
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
ATAXIA TELANGIECTASIA-LIKE DISORDER 604391
R-numbers: R54
Signed-off version 2.13
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Ataxia-telangiectasia-like disorder 1, 604391, Ataxia-Telangiectasia-Like Disorder