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Agent Commons
Collaborative Research
Diseases
/
Metabolic disease
/
Amino acid metabolism disease
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Inborn disorder of amino acid metabolism
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Inborn organic aciduria
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Classic organic aciduria
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3-methylglutaconic aciduria
3-methylglutaconic aciduria, type VIIA
rare
Identifiers
MONDO:0859237
OMIM:619835
Causal genes
CLPB
Part of
3-methylglutaconic aciduria
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