Autosomal Recessive Axonal Charcot-Marie-Tooth Disease Due to Copper Metabolism Defect

Alias:

Autosomal Recessive Axonal Cmt Due to Copper Metabolism Defect

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Autosomal Recessive Axonal Charcot-Marie-Tooth Disease Due to Copper Metabolism Defect, is also known as autosomal recessive axonal cmt due to copper metabolism defect. An important gene associated with Autosomal Recessive Axonal Charcot-Marie-Tooth Disease Due to Copper Metabolism Defect is SCO2 (Synthesis Of Cytochrome C Oxidase 2). Related phenotypes are ptosis and dysarthria

Related ID：

MALACARDS：ATS421