RS148232621 PLEKHG5
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Associated Conditions
Neuronopathy
distal hereditary motor
autosomal recessive 4
Charcot-Marie-Tooth disease recessive intermediate C
Inborn genetic diseases
Neuronopathy
distal hereditary motor
autosomal recessive 4
Charcot-Marie-Tooth disease recessive intermediate C
Inborn genetic diseases
Other Variants in PLEKHG5