All diseases

OMIM ID
217400
OMIM term:
CORNEAL DYSTROPHY AND PERCEPTIVE DEAFNESS
Alternative terms:
CDPD
CDPD1
CORNEAL DYSTROPHY AND SENSORINEURAL DEAFNESS
HARBOYAN SYNDROME
(∗) Location:
20p13  
(†) Associated OMIM genes:
SLC4A11  
(‡) Associated MGI genes:

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* quick link - http://q.sanger.ac.uk/e9jsgv9u