All diseases

OMIM ID
612736
OMIM term:
GUANIDINOACETATE METHYLTRANSFERASE DEFICIENCY
Alternative terms:
GAMT DEFICIENCY
CREATINE DEFICIENCY SYNDROME DUE TO GAMT DEFICIENCY
(∗) Location:
19p13.3  
(†) Associated OMIM genes:
GAMT  
(‡) Associated MGI genes:
Gamt  

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* quick link - http://q.sanger.ac.uk/va4vaepx