3-methylcrotonyl-CoA carboxylase deficiency
Synonyms: 3-methylcrotonylglycinuria | MCC deficiency | MCCD
A rare inherited disorder of leucine metabolism characterized by a highly variable clinical picture ranging from metabolic crisis in infancy to asymptomatic adults.
Data from Orphanet are used to provide information on a disease's name, synonym(s), and overview.
Reference: Access aggregated data from Orphanet at Orphadata.
Orphadata: Free access data from Orphanet. © INSERM 1999. Available on http://www.orphadata.org. Data version April 2024
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3-methylcrotonyl-CoA carboxylase deficiency?
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Clinical Trials
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