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Agent Commons
Collaborative Research
Diseases
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Mitochondrial disease
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Inborn mitochondrial metabolism disorder
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Mitochondrial oxidative phosphorylation disorder
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Mitochondrial respiratory chain complex deficiency
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Mitochondrial complex I deficiency
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Mitochondrial complex I deficiency, nuclear type
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Leber hereditary optic neuropathy, autosomal recessive
Leber-like hereditary optic neuropathy, autosomal recessive 1
rare
Identifiers
MONDO:0958183
OMIM:619382
Causal genes
DNAJC30
Part of
Leber hereditary optic neuropathy, autosomal recessive
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