mitochondrial complex IV deficiency, nuclear type 18

Rare Disease

MONDO:0033653

Also Known As

MC4DN18mitochondrial complex IV deficiency, nuclear type 18

Any mitochondrial complex IV deficiency in which the cause of the disease is a mutation in the COX6A2 gene.

Comprehensive, easy-to-understand information about this condition

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Gene data from MyGene.info • Click to view on NCBI Gene

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MONDO:0033638

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MONDO:0033639