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Multiple mitochondrial dysfunctions syndrome 1
MONDO:0011582Any fatal multiple mitochondrial dysfunctions syndrome in which the cause of the disease is a mutation in the NFU1 gene.
Also known as: Mmds, NFU1 deficiency, NFU1 fatal multiple mitochondrial dysfunctions syndrome, fatal multiple mitochondrial dysfunctions syndrome caused by mutation in NFU1, multiple mitochondrial dysfunctions syndrome 1, multiple mitochondrial dysfunctions syndrome type 1, MMDS1
50 clinical trials for this condition and its sub-types.
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Disease
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Metabolic disease
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Hereditary disease
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Inherited lipid metabolism disorder
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Inborn mitochondrial metabolism disorder
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Inborn errors of metabolism
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Mitochondrial disease
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Human disease
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Developmental defect during embryogenesis
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Inherited fatty acid metabolism disorder
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