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Up to: Disease by developmental or physiological process

Mitochondrial disease

40 trials tagged with this condition →

Inborn mitochondrial metabolism disorder 59 trials · 127 incl. sub-types Sub-types →
ACO2-related optic atrophy with or without extraocular features 0 trials Sub-types →
Bjornstad syndrome 0 trials
FDXR-related optic atrophy mitochondrial dysfunction syndrome 0 trials Sub-types →
GRACILE syndrome 0 trials
X-linked sideroblastic anemia with ataxia 0 trials
Autosomal dominant optic atrophy plus syndrome 0 trials Sub-types →
Ethylmalonic encephalopathy 0 trials
Hereditary myopathy with lactic acidosis due to ISCU deficiency 0 trials
Maternally-inherited cardiomyopathy and hearing loss 0 trials
Mitochondrial short-chain Enoyl-Coa hydratase 1 deficiency 0 trials
Pure mitochondrial myopathy 0 trials