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Dimethylglycine dehydrogenase deficiency

MONDO:0011610

An extremely rare autosomal recessive glycine metabolism disorder characterized clinically in the single reported case to date by muscle fatigue and a fish-like odor. This is an n-of-1 use case where only one patient or family has been described with this disorder.

Also known as: DMG dehydrogenase deficiency, DMGDH deficiency, dimethylglycine dehydrogenase activity disease, dimethylglycine dehydrogenase deficiency, disorder of dimethylglycine dehydrogenase activity, DMGDHD, Dmgdh deficiency

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

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Sub-types

Trimethylaminuria (1) Secondary trimethylaminuria (0) Severe primary trimethylaminuria (0)

Broader categories

Disease (618) Metabolic disease (215) Hereditary disease (172) Inborn errors of metabolism (42) Human disease (14) Disease of genetic or genomic mechanism (2) Disease by developmental or physiological process (0) Disease by etiologic mechanism (0) Disorder of methylamine metabolism (0) Disorder of peptide and amine metabolism (0)
Trials to join now! 13 Not yet recruiting 3 Not yet finished but already full! 3 Completed 6
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