All diseases

OMIM ID
607364
OMIM term:
BARTTER SYNDROME, TYPE 3
Alternative terms:

(∗) Location:
1p36.13  
(†) Associated OMIM genes:
CLCNKB  
(‡) Associated MGI genes:

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Choose a gene on the left to see models here.
* quick link - http://q.sanger.ac.uk/lmjm9ae2