disease has basis in dysfunction of mitochondrion inborn mitochondrial metabolism disorder https://rarediseases.info.nih.gov/diseases/7048/mitochondrial-genetic-disorders https://www.malacards.org/card/mitochondrial_disease https://www.malacards.org/card/mitochondrial_metabolism_disease NANDO:1200173 MEDGEN:1778113 UMLS:C1456275 MONDO:0004069 MESH:D028361 GARD:0018887 mitochondrial genetic disorders mitochondrial disease DOID:700 NANDO:2100163 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. Orphanet:68380 developmental anomaly of metabolic origin inborn errors of metabolism inborn disorder of energy metabolism mitochondrial disease