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Up to: Developmental anomaly of metabolic origin · Inborn disorder of energy metabolism · Mitochondrial disease

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.

59 trials tagged with this condition →

Mitochondrial oxidative phosphorylation disorder 3 trials · 58 incl. sub-types Sub-types →
Inborn mitochondrial myopathy 18 trials · 45 incl. sub-types Sub-types →
Pyruvate dehydrogenase deficiency 2 trials · 4 incl. sub-types Sub-types →
Histiocytoid cardiomyopathy 3 trials Sub-types →
Fumaric aciduria 2 trials
OPA1-related optic atrophy with or without extraocular features 1 trial Sub-types →
Multiple acyl-CoA dehydrogenase deficiency 1 trial Sub-types →
Inherited lipoic acid biosynthesis defect 0 trials · 1 incl. sub-types Sub-types →
3-methylglutaconic aciduria with deafness, encephalopathy, and Leigh-like syndrome 0 trials
HSD10 mitochondrial disease 0 trials Sub-types →
Hypotonia-cystinuria syndrome 0 trials Sub-types →
Mitochondrial membrane transport disorder 0 trials Sub-types →
Mitochondrial pyruvate carrier deficiency 0 trials
Oxoglutaricaciduria 0 trials