Terminology Service for NFDI4Health

inborn mitochondrial metabolism disorder

Go to external page http://purl.obolibrary.org/obo/MONDO_0004069


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

Label

inborn mitochondrial metabolism disorder

database cross reference
Subsets

gard_rare, disease_grouping, ordo_group_of_disorders

exactMatch

http://purl.obolibrary.org/obo/Orphanet_68380, http://purl.obolibrary.org/obo/DOID_700, http://identifiers.org/mesh/D028361

has broad synonym

mitochondrial disease

has related synonym

mitochondrial genetic disorders, mitochondrial metabolism disease

id

MONDO:0004069

see also

https://rarediseases.info.nih.gov/diseases/7048/mitochondrial-genetic-disorders