All diseases

OMIM ID
601678
OMIM term:
BARTTER SYNDROME, ANTENATAL, TYPE 1
Alternative terms:
HYPOKALEMIC ALKALOSIS WITH HYPERCALCIURIA, ANTENATAL, 1
HYPERPROSTAGLANDIN E SYNDROME 1
(∗) Location:
15q21.1  
(†) Associated OMIM genes:
SLC12A1  
(‡) Associated MGI genes:
Slc12a1  

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* quick link - http://q.sanger.ac.uk/bpan5osw