inborn mitochondrial metabolism disorder
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. [ http://id.nlm.nih.gov/mesh/D028361 ]
Term info
inborn mitochondrial metabolism disorder
gard_rare, disease_grouping, ordo_group_of_disorders
http://purl.obolibrary.org/obo/Orphanet_68380, http://purl.obolibrary.org/obo/DOID_700, http://identifiers.org/mesh/D028361
mitochondrial disease
mitochondrial genetic disorders, mitochondrial metabolism disease
MONDO:0004069
https://rarediseases.info.nih.gov/diseases/7048/mitochondrial-genetic-disorders