Charcot-Marie-Tooth disease recessive intermediate D

MONDO:0014467

Any Charcot-Marie-Tooth disease in which the cause of the disease is a mutation in the COX6A1 gene.

Also known as: CMTRID, COX6A1 Charcot-Marie-Tooth disease, Charcot-Marie-Tooth disease caused by mutation in COX6A1, Charcot-Marie-Tooth disease recessive intermediate type D, Charcot-Marie-Tooth disease, recessive Intermediate type D, RI-CMT type D, autosomal recessive intermediate Charcot-Marie-Tooth disease type D, Charcot-Marie-Tooth disease, recessive intermediate D

22 clinical trials for this condition and its sub-types, 0 tagged with Charcot-Marie-Tooth disease recessive intermediate D itself.

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↑ Mitochondrial oxidative phosphorylation disorder (58) ↑ Autosomal recessive intermediate Charcot-Marie-Tooth disease (2)

Including sub-types (22) Tagged with Charcot-Marie-Tooth disease recessive intermediate D (0)

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