All diseases

OMIM ID
103500
OMIM term:
TIETZ SYNDROME
Alternative terms:
ALBINISM-DEAFNESS OF TIETZ
HYPOPIGMENTATION/DEAFNESS OF TIETZ
TIETZ ALBINISM-DEAFNESS SYNDROME
(∗) Location:
3p14-p13  
(†) Associated OMIM genes:
MITF  
(‡) Associated MGI genes:
Mitf  

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* quick link - http://q.sanger.ac.uk/0ldmevkh