Any nephrotic syndrome in which the cause of the disease is a mutation in the NPHS2 gene.
Comprehensive, easy-to-understand information about this condition
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focal segmental glomerulosclerosis 1
MONDO:0011303
nephrotic syndrome, type 3
MONDO:0012546
nephrotic syndrome, type 6
MONDO:0013619
familial steroid-resistant nephrotic syndrome with sensorineural deafness
MONDO:0013836
nephrotic syndrome, type 8
MONDO:0014099
nephrotic syndrome, type 9
MONDO:0014257