Severe primary trimethylaminuria
MONDO:0018767Any trimethylaminuria in which the cause of the disease is a mutation in the FMO3 gene.
Also known as: trimethylaminuria, TMAU, TMAuria, fish malodor syndrome, fish odor syndrome, fish odour syndrome, fish-odor syndrome, stale fish syndrome
0 clinical trials for this condition and its sub-types.
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Disease
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Metabolic disease
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Hereditary disease
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Inborn errors of metabolism
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Human disease
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Disease of genetic or genomic mechanism
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Trimethylaminuria
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Dimethylglycine dehydrogenase deficiency
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Disease by developmental or physiological process
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