3-methylcrotonyl-CoA carboxylase 2 deficiency
MONDO:0008862Any 3-methylcrotonyl-CoA carboxylase deficiency in which the cause of the disease is a mutation in the MCCC2 gene.
Also known as: 3-Methylcrotonyl-CoA carboxylase 2 deficiency, 3-methylcrotonyl-CoA carboxylase deficiency caused by mutation in MCCC2, MCCC2 3-methylcrotonyl-CoA carboxylase deficiency, 3 alpha methylcrotonyl-CoA carboxylase 2 deficiency, 3 alpha methylcrotonylglycinuria 2, 3-METHYLCROTONYL-CoA carboxylase 2 deficiency, 3-methylcrotonylglycinuria 2, MCC 2 deficiency
1 clinical trial for this condition and its sub-types.
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Disease
(680)
Metabolic disease
(233)
Hereditary disease
(176)
Inborn errors of metabolism
(45)
Human disease
(14)
Inborn organic aciduria
(5)
Inborn disorder of amino acid metabolism
(4)
Disease of genetic or genomic mechanism
(2)
Amino acid metabolism disease
(1)
3-methylcrotonyl-CoA carboxylase deficiency
(0)