You are using an outdated browser. Please upgrade your browser to improve your experience.

X-linked recessive mitochondrial myopathy

Disease Summary
Associated Targets (0)

Explore Associated Targets
Mondo Description A mitochondrial myopathy caused by defects in the MICOS subunit gene APOO (MIC26). Modelling in yeast and flies demonstrate an inability to insert MICOS complex into the inner mitohondrial membrane. Associated symptoms include, lactic acidosis, cognitive impairment and autistic features.
Mondo Term and Equivalent IDs
MONDO:0100138:  X-linked recessive mitochondrial myopathy
GWAS Targets (0)
No GWAS traits found
Target Novelty (Tin-x)
No novelty measurements found