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Familial nephrotic syndrome

MONDO:0002350

An instance of nephrotic syndrome that is caused by an inherited modification of the individual's genome.

Also known as: congenital nephrotic syndrome, hereditary nephrotic syndrome

30 clinical trials for this condition and its sub-types.

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Sub-types

Immunoglobulin-mediated membranoproliferative glomerulonephritis (9) Idiopathic multidrug-resistant nephrotic syndrome (6) Nephrotic syndrome 14 (2) Nephrotic syndrome, type 4 (1) Congenital nephrotic syndrome, Finnish type (0) Familial idiopathic steroid-resistant nephrotic syndrome (0) Familial idiopathic steroid-resistant nephrotic syndrome with diffuse mesangial proliferation (0) Familial idiopathic steroid-resistant nephrotic syndrome with diffuse mesangial sclerosis (0) Familial idiopathic steroid-resistant nephrotic syndrome with minimal changes (0) Familial steroid-resistant nephrotic syndrome with sensorineural deafness (0) Focal segmental glomerulosclerosis 1 (0) LAMB2-related infantile-onset nephrotic syndrome (0) Nephrotic syndrome 15 (0) Nephrotic syndrome 16 (0) Nephrotic syndrome, IIa 26 (0) Nephrotic syndrome, type 10 (0) Nephrotic syndrome, type 11 (0) Nephrotic syndrome, type 12 (0) Nephrotic syndrome, type 13 (0) Nephrotic syndrome, type 17 (0)

Broader categories

Disease (618) Kidney disorder (202) Hereditary disease (172) Urinary system disorder (62) Nephrotic syndrome (41) Syndromic disease (24) Human disease (14) Disease of genetic or genomic mechanism (2) Disease by body system or component (0) Disease by etiologic mechanism (0)
Trials to join now! 18 Not yet recruiting 3 Not yet finished but already full! 6 Completed 3
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