All diseases

OMIM ID
600995
OMIM term:
NEPHROTIC SYNDROME, TYPE 2; NPHS2
Alternative terms:

(∗) Location:
1q25.2  
(†) Associated OMIM genes:
NPHS2  
(‡) Associated MGI genes:
Arhgdia   Mpv17   Nphs2  

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* quick link - http://q.sanger.ac.uk/a4lkq1oi