Inborn mitochondrial metabolism disorder
MONDO:0004069Diseases 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.
Also known as: mitochondrial disease, mitochondrial genetic disorders, mitochondrial metabolism disease
148 clinical trials for this condition and its sub-types.
Follow this condition — get notified about new trialsSub-types
Leber hereditary optic neuropathy
(17)
Inborn mitochondrial myopathy
(15)
MELAS syndrome
(12)
Leigh syndrome
(7)
Barth syndrome
(4)
Deafness, aminoglycoside-induced
(4)
Kearns-Sayre syndrome
(4)
MERRF syndrome
(4)
Mitochondrial respiratory chain complex deficiency
(4)
Autosomal dominant optic atrophy, classic form
(3)
Histiocytoid cardiomyopathy
(3)
Maternally-inherited diabetes and deafness
(3)
Mitochondrial DNA depletion syndrome
(3)
Mitochondrial DNA depletion syndrome 4a
(3)
Mitochondrial DNA depletion syndrome, myopathic form
(3)
Mitochondrial encephalomyopathy
(3)
Mitochondrial neurogastrointestinal encephalomyopathy
(3)
Mitochondrial oxidative phosphorylation disorder
(3)
Mitochondrial trifunctional protein deficiency
(3)
Myopathy, lactic acidosis, and sideroblastic anemia
(3)
Broader categories
Disease
(618)
Metabolic disease
(215)
Hereditary disease
(172)
Inborn errors of metabolism
(42)
Mitochondrial disease
(39)
Human disease
(14)
Developmental defect during embryogenesis
(7)
Disease of genetic or genomic mechanism
(2)
Inborn disorder of energy metabolism
(1)
Developmental anomaly of metabolic origin
(0)