All diseases

OMIM ID
210200
OMIM term:
3-@METHYLCROTONYL-CoA CARBOXYLASE 1 DEFICIENCY
Alternative terms:
MCCD TYPE 1
MCC1 DEFICIENCY
3-@METHYLCROTONYLGLYCINURIA I
METHYLCROTONYLGLYCINURIA TYPE I
(∗) Location:
3q27.1  
(†) Associated OMIM genes:
MCCC1  
(‡) Associated MGI genes:

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* quick link - http://q.sanger.ac.uk/k39rirvi