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Glutaric acidemia IIb

MONDO:0700074

Any multiple acyl-CoA dehydrogenase deficiency in which the cause of the disease is a mutation in the ETFB gene.

Also known as: ETFB deficiency, GA2B, glutaric acidemia 2B, multiple acyl-CoA dehydrogenase deficiency caused by mutation in ETFB

20 clinical trials for this condition and its sub-types.

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Broader categories

Cardiovascular disorder (1051) Disease (680) Heart disorder (300) Metabolic disease (233) Musculoskeletal system disorder (207) Inherited lipid metabolism disorder (189) Hereditary disease (176) Cardiomyopathy (144) Hypertrophic cardiomyopathy (112) Inborn mitochondrial metabolism disorder (58)
Trials to join now! 10 Not yet recruiting 1 Not yet finished but already full! 6 Completed 2 Terminated 1
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  • 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…

    Phase: NA • Sponsor: Centre Hospitalier Universitaire de Nice • Aim: Diagnosis

    Last updated Jun 27, 2026 12:04 UTC

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