SDHC-related Mitochondrial Disease

MONDO:0700347

Mitochondrial complex II deficiency due to pathogenic variants in the SDHC gene, resulting in a variety of clinical manifestations, including neurological and muscular symptoms.

Also known as: SDHC-related Mitochondrial Disease

13 clinical trials for this condition and its sub-types, 0 tagged with SDHC-related Mitochondrial Disease itself.

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Where it sits in the disease tree

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Part of

↑ Mitochondrial respiratory chain complex deficiency (5)

Including sub-types (13) Tagged with SDHC-related Mitochondrial Disease (0)

We haven't found any trials for this condition yet. Follow it to get notified when new trials appear.