All diseases

OMIM ID
124900
OMIM term:
DEAFNESS, AUTOSOMAL DOMINANT 1; DFNA1
Alternative terms:
HEREDITARY LOW FREQUENCY HEARING LOSS; LFHL1
DEAFNESS, PROGRESSIVE LOW TONE
KONIGSMARK SYNDROME
(∗) Location:
5q31.3  
(†) Associated OMIM genes:
DIAPH1  
(‡) Associated MGI genes:

*Loading mouse genes ...

*Loading zebrafish genes ...

Choose a gene on the left to see models here.
* quick link - http://q.sanger.ac.uk/eckytm08