Skip navigation

Official websites use .gov
A .gov website belongs to an official government organization in the United States.

Secure .gov websites use HTTPS
A lock ( ) or https:// means you’ve safely connected to the .gov website. Share sensitive information only on official, secure websites.

Results 1 - 8 of 8 for Nephrotic Syndrome
  1. NPHS2 gene 
    ... NPHS2 gene have been found to cause congenital nephrotic syndrome. This condition is a kidney disorder that begins ... to be the most frequent cause of congenital nephrotic syndrome. Most NPHS2 gene mutations change single protein building ...
    https://medlineplus.gov/genetics/gene/nphs2 - Genetics
  2. NPHS1 gene 
    ... NPHS1 gene have been found to cause congenital nephrotic syndrome. This condition is a kidney disorder that begins ... gene mutations account for all cases of congenital nephrotic syndrome of the Finnish type. This form of the ...
    https://medlineplus.gov/genetics/gene/nphs1 - Genetics
  3. WT1 gene 
    ... Health Condition MedlinePlus Genetics provides information about Congenital nephrotic syndrome More About This Health Condition MedlinePlus Genetics provides ...
    https://medlineplus.gov/genetics/gene/wt1 - Genetics
  4. KANK2 gene 
    ... families with a form of kidney disease called nephrotic syndrome. This condition is characterized by an inability of ... F. KANK deficiency leads to podocyte dysfunction and nephrotic syndrome. J Clin Invest. 2015 Jun;125(6):2375- ...
    https://medlineplus.gov/genetics/gene/kank2 - Genetics
  5. SCARB2 gene 
    ... 2 gene associated with progressive myoclonic epilepsy and nephrotic syndrome. Hum Mol Genet. 2008 Jul 15;17(14): ...
    https://medlineplus.gov/genetics/gene/scarb2 - Genetics
  6. COQ8B gene 
    ... C, Hildebrandt F. ADCK4 mutations promote steroid-resistant nephrotic syndrome through CoQ10 biosynthesis disruption. J Clin Invest. 2013 ...
    https://medlineplus.gov/genetics/gene/coq8b - Genetics
  7. COQ6 gene 
    ... Hildebrandt F. COQ6 mutations in human patients produce nephrotic syndrome with sensorineural deafness. J Clin Invest. 2011 May; ...
    https://medlineplus.gov/genetics/gene/coq6 - Genetics
  8. FGA gene 
    ... 000093566. Citation on PubMed Picken MM, Linke RP. Nephrotic syndrome due to an amyloidogenic mutation in fibrinogen A ...
    https://medlineplus.gov/genetics/gene/fga - Genetics