Nephrotic syndrome, type 13
MONDO:0014818Any familial nephrotic syndrome in which the cause of the disease is a mutation in the NUP205 gene.
Also known as: NPHS13, NUP205 familial nephrotic syndrome, familial nephrotic syndrome caused by mutation in NUP205, nephrotic syndrome, type 13, nephrotic syndrome, type 13; NPHS13
4 clinical trials for this condition and its sub-types, 0 tagged with Nephrotic syndrome, type 13 itself.
Follow this condition to get notified about new trialsWhere it sits in the disease tree
Browse by category →We haven't found any trials for this condition yet. Follow it to get notified when new trials appear.