Action Myoclonus Renal Failure SyndromeACTN4 Alpha actinin4Calcium (Physiology renal)CD151 TetraspaninCD2APCoenzyme Q10Congenital nephrotic syndrome finnish typeCOQ2Denys Drash syndromeEarly onset familial nephrotic syndromeEpstein s syndromeFechtner s syndromeFrasier s syndrome
Galloway Mowat s syndromeGlomerulopathy (Collapsing)GMS1Hypomagnesemia with hypercalciuria familiarIon channel (TRP Family)Kidney (Diseases viral HIV HIVAN)Kidney (FSGS)Kidney (Minimal change nephrotic syndrome)Kidney (Podocytes)Kidney (Polycystic kidney disease)LAMB2 Laminin beta2LamininLMNA Lamin C Prelamin A
LMX1BMandibuloacral dysplasiaMay Hegglin anomalyMYH9Nail patella syndromeNPHS1 NephrinNPHS2OsmosensorPhospholipase C epsilonPierson s syndromePLCE1PodocinRituximab ttCD20
SCARB2Schimke immunoosseous dysplasiaSebastian s syndromeSMARCALISteroid resistant nephrotic syndrome SRN1TRPC6TRPM6TRPP2TRPV4TRPV5WT1ZMPSTE24
Downloaded from http://www.kidney.de - The Database of Free Medical Reviews - The Metatextbook of Medicine - Ossip Groth
All Medline data shown were primarily retrieved from MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.