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)

Trials to join now! 5 Not yet recruiting 1 Not yet finished but already full! 4 Completed 2 Terminated 1

New DNA test could end years of uncertainty for mitochondrial disease patients

Diagnosis Not yet recruiting

This pilot study aims to develop a new digital PCR technique to more accurately diagnose mitochondrial diseases. Researchers will test the method on blood, urine, saliva, and muscle fiber samples from 4 patients. If validated, the technique could be faster and cheaper than curren…

Sponsor: Centre Hospitalier Universitaire de Nice • Aim: Diagnosis

Last updated Jun 27, 2026 12:04 UTC

SDHC-related Mitochondrial Disease

Where it sits in the disease tree

New DNA test could end years of uncertainty for mitochondrial disease patients