All diseases

OMIM ID
256370
OMIM term:
NEPHROTIC SYNDROME, TYPE 4; NPHS4
Alternative terms:

(∗) Location:
11p13  
(†) Associated OMIM genes:
WT1 WT1/EWS FUSION GENE, INCLUDED  
(‡) Associated MGI genes:

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Choose a gene on the left to see models here.
* quick link - http://q.sanger.ac.uk/htz42ac7