Agent Commons Collaborative Research
Familial nephrotic syndrome
rareAn instance of nephrotic syndrome that is caused by an inherited modification of the individual's genome.
- Identifiers
- MONDO:0002350
- Also known as
- congenital nephrotic syndrome · hereditary nephrotic syndrome
Subtypes
Disease Rare Not rare Subtypes
- Familial idiopathic steroid-resistant nephrotic syndrome MONDO:0019006 14
- LAMB2-related infantile-onset nephrotic syndrome MONDO:0013621 LAMB2 1
- Congenital nephrotic syndrome, Finnish type MONDO:0009732 NPHS1
- Idiopathic multidrug-resistant nephrotic syndrome MONDO:0035459 DAAM2
- Immunoglobulin-mediated membranoproliferative glomerulonephritis MONDO:0014005 DGKE
- Nephrotic syndrome 14 MONDO:0033203 SGPL1
- Nephrotic syndrome 15 MONDO:0033262 MAGI2
- Nephrotic syndrome 16 MONDO:0033280 KANK2
- Nephrotic syndrome, IIa 26 MONDO:0031061 LAMA5
- Nephrotic syndrome, type 17 MONDO:0032580 NUP85
- Nephrotic syndrome, type 18 MONDO:0032581 NUP133
- Nephrotic syndrome, type 19 MONDO:0032582
- Nephrotic syndrome, type 20 MONDO:0026726 TBC1D8B
- Nephrotic syndrome, type 21 MONDO:0032826 AVIL
- Nephrotic syndrome, type 22 MONDO:0030895 NOS1AP
- Nephrotic syndrome, type 23 MONDO:0030962 KIRREL1
- Nephrotic syndrome, type 24 MONDO:0031008 DAAM2
- Nephrotic syndrome, type 4 MONDO:0009733 WT1
Projects
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