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Results 1 - 6 of 6 for Nephrotic "syndrome," type 6
  1. Primary coenzyme Q10 deficiency 
    ... 1; COQ10D1 COENZYME Q10 DEFICIENCY, PRIMARY, 4; COQ10D4 NEPHROTIC SYNDROME, TYPE 9; NPHS9 COENZYME Q10 DEFICIENCY, PRIMARY, 8; COQ10D8 COENZYME Q10 DEFICIENCY, PRIMARY, 6; COQ10D6 COENZYME Q10 DEFICIENCY, PRIMARY, 2; COQ10D2 COENZYME ...
    https://medlineplus.gov/.../primary-coenzyme-q10-deficiency - Genetics
  2. Congenital nephrotic syndrome 
    ... Registry: Finnish congenital nephrotic syndrome Genetic Testing Registry: Nephrotic syndrome, type 2 Congenital nephrotic syndrome, Finnish type National Organization ...
    https://medlineplus.gov/.../condition/congenital-nephrotic-syndrome - Genetics
  3. NPHS1 gene 
    ... Alpers CE. AJKD Atlas of Renal Pathology: Congenital Nephrotic Syndrome of Finnish Type. Am J Kidney Dis. 2015 Sep;66(3): ... in a worldwide cohort of patients with congenital nephrotic syndrome (CNS). Nephrol Dial Transplant. 2010 Sep;25(9):2970-6. doi: 10.1093/ndt/gfq088. Epub 2010 Feb ...
    https://medlineplus.gov/genetics/gene/nphs1 - Genetics
  4. KANK2 gene 
    ... F. KANK deficiency leads to podocyte dysfunction and nephrotic syndrome. J Clin Invest. 2015 Jun;125(6):2375-84. doi: 10.1172/JCI79504. Epub 2015 ...
    https://medlineplus.gov/genetics/gene/kank2 - Genetics
  5. Action myoclonus–renal failure syndrome 
    ... 2 gene associated with progressive myoclonic epilepsy and nephrotic syndrome. Hum Mol Genet. 2008 Jul 15;17(14): ... failure. Ann Neurol. 2009 Oct;66(4):532-6. doi: 10.1002/ana.21765. Citation on PubMed ... failure syndrome and evaluation of SCARB2 mutations in isolated AMRF ...
    https://medlineplus.gov/.../action-myoclonus-renal-failure-syndrome - Genetics
  6. 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