All diseases

OMIM ID
223360
OMIM term:
DOPAMINE BETA-HYDROXYLASE DEFICIENCY, CONGENITAL
Alternative terms:
NOREPINEPHRINE DEFICIENCY
NORADRENALINE DEFICIENCY
(∗) Location:
9q34.2  
(†) Associated OMIM genes:
DBH  
(‡) Associated MGI genes:
Dbh  

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* quick link - http://q.sanger.ac.uk/n7yxyvtl