RS145899734 SYNE1
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Associated Conditions
Autosomal recessive ataxia
Beauce type
Emery-Dreifuss muscular dystrophy 4
autosomal dominant
Intellectual disability
Arthrogryposis multiplex congenita 3
myogenic type
Inborn genetic diseases
SYNE1-related disorder
Autosomal recessive ataxia
Beauce type
Emery-Dreifuss muscular dystrophy 4
autosomal dominant
Intellectual disability
Arthrogryposis multiplex congenita 3
Other Variants in SYNE1