RS777387819 DYNC1H1

Health Risk Chr 14:101994241

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Associated Conditions

Charcot-Marie-Tooth disease axonal type 2O

Autosomal dominant childhood-onset proximal spinal muscular atrophy without contractures

Intellectual disability

autosomal dominant 13

Inborn genetic diseases

Charcot-Marie-Tooth disease axonal type 2O

Autosomal dominant childhood-onset proximal spinal muscular atrophy without contractures

Intellectual disability

autosomal dominant 13

Inborn genetic diseases

Other Variants in DYNC1H1