disease has basis in dysfunction of mitochondrion inborn mitochondrial metabolism disorder DOID:700 Diseases caused by abnormal function of the mitochondria. They may be caused by mutations, acquired or inherited, in mitochondrial dna or in nuclear genes that code for mitochondrial components. They may also be the result of acquired mitochondria dysfunction due to adverse effects of drugs, infections, or other environmental causes. GARD:0007048 MESH:D028361 MONDO:0004069 Orphanet:68380 https://rarediseases.info.nih.gov/diseases/7048/mitochondrial-genetic-disorders mitochondrial disease mitochondrial genetic disorders mitochondrial metabolism disease developmental anomaly of metabolic origin inborn errors of metabolism inborn disorder of energy metabolism mitochondrial disease