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Multiple mitochondrial dysfunctions syndrome 1

MONDO:0011582

Any 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

14 clinical trials for this condition and its sub-types, 0 tagged with Multiple mitochondrial dysfunctions syndrome 1 itself.

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