All diseases

OMIM ID
605594
OMIM term:
DEAFNESS, AUTOSOMAL DOMINANT 39, WITH DENTINOGENESIS IMPERFECTA 1
Alternative terms:
DFNA39/DENTINOGENESIS IMPERFECTA 1 SYNDROME
DFNA39/DGI1 SYNDROME
DGI1/DFNA39 SYNDROME
(∗) Location:
4q22.1  
(†) Associated OMIM genes:
DSPP DENTIN PHOSPHOPROTEIN, INCLUDED; DPP, INCLUDED  
(‡) Associated MGI genes:

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* quick link - http://q.sanger.ac.uk/tvr45tad