All diseases

OMIM ID
210210
OMIM term:
3-@METHYLCROTONYL-CoA CARBOXYLASE 2 DEFICIENCY
Alternative terms:
MCC2 DEFICIENCY
3-@METHYLCROTONYLGLYCINURIA II
METHYLCROTONYLGLYCINURIA, TYPE II
(∗) Location:
5q13.2  
(†) Associated OMIM genes:
MCCC2  
(‡) Associated MGI genes:

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