All diseases

OMIM ID
256300
OMIM term:
NEPHROTIC SYNDROME, TYPE 1; NPHS1
Alternative terms:
FINNISH CONGENITAL NEPHROSIS; CNF
NEPHROTIC SYNDROME, CONGENITAL
(∗) Location:
19q13.12  
(†) Associated OMIM genes:
NPHS1  
(‡) Associated MGI genes:
Nphs1  

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* quick link - http://q.sanger.ac.uk/as0e6fd1