All diseases

OMIM ID
250850
OMIM term:
METHIONINE ADENOSYLTRANSFERASE DEFICIENCY
Alternative terms:
MAT DEFICIENCY
MAT I/III DEFICIENCY
HYPERMETHIONINEMIA, ISOLATED PERSISTENT
(∗) Location:
10q23.1  
(†) Associated OMIM genes:
MAT1A  
(‡) Associated MGI genes:
Mat1a  

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* quick link - http://q.sanger.ac.uk/4wwao8i3