Action Myoclonus Renal Failure SyndromeACTN4 Alpha actinin4CD151 TetraspaninCD2APCharcot Marie Tooth disease type 2bCoenzyme Q10Congenital nephrotic syndrome finnish typeCOQ2Denys Drash syndromeEarly onset familial nephrotic syndromeEmery Dreifuss dystrophyEpstein s syndromeFechtner s syndrome
Frasier s syndromeGalloway Mowat s syndromeGMS1Greenberg HEM dysplasiaKidney (FSGS)LAMB2 Laminin beta2LaminLamininLaminopathyLeukodystrophyLipodystrophyLipodystrphy Dunnigan typeLMNA Lamin C Prelamin A
LMNB1 Lamin B1LMNB2 Lamin B2LMX1BMandibuloacral dysplasiaMay Hegglin anomalyMYH9Nail patella syndromeNPHS1 NephrinNPHS2Pelger Huet anomalyPhospholipase C epsilonPierson s syndromePLCE1
PodocinSCARB2Schimke immunoosseous dysplasiaSebastian s syndromeSMARCALISteroid resistant nephrotic syndrome SRN1TRPC6WT1ZMPSTE24
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.