General Information of Disease (ID: DISP5E0H)

Disease Name Inborn mitochondrial metabolism disorder
Synonyms mitochondrial metabolism disease; mitochondrial genetic disorders; mitochondrial disease
Definition
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.
Disease Hierarchy
DISMFQKM: Developmental anomaly of metabolic origin
DISO5FAY: Inborn error of metabolism
DIS0J9MR: Inborn disorder of energy metabolism
DISKAHA3: Mitochondrial disease
DISP5E0H: Inborn mitochondrial metabolism disorder
Disease Identifiers
MONDO ID
MONDO_0004069
UMLS CUI
C1456275
MedGen ID
1778113