RS773630385 DYNC1H1

Health Risk Chr 14:102005150

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Associated Conditions

Autosomal dominant childhood-onset proximal spinal muscular atrophy without contractures

Intellectual disability

autosomal dominant 13

Charcot-Marie-Tooth disease axonal type 2O

Autosomal dominant childhood-onset proximal spinal muscular atrophy without contractures

Intellectual disability

autosomal dominant 13

Charcot-Marie-Tooth disease axonal type 2O

Other Variants in DYNC1H1