All diseases

OMIM ID
229100
OMIM term:
FORMIMINOTRANSFERASE DEFICIENCY
Alternative terms:
GLUTAMATE FORMIMINOTRANSFERASE DEFICIENCY
FORMIMINOGLUTAMIC ACIDURIA
FIGLU-URIA
(∗) Location:
21q22.3  
(†) Associated OMIM genes:
FTCD  
(‡) Associated MGI genes:

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* quick link - http://q.sanger.ac.uk/4amz8ytg