ABCC8 SUR1AidsAnemia (megaloblastic thiamine responsive)Bererdinelli Seip congenital lipodystrophyBSCL1 AGPAT2BSCL2 SeipinCharcot Marie Tooth disease type 2bDiabetes mellitus (Hereditary MODY)Diabetes mellitus (hereditary)Diabetes mellitus (neonatal)Donohue s syndrome LeprechaunismEIF2AK3 PERK
Emery Dreifuss dystrophyFRDA1 FrataxinFriedreich ataxiaGlucokinaseGLUD1Greenberg HEM dysplasiaInsulin resistance type aKCNJ11 Kir6 2LaminopathyLeptinLeukodystrophyLipodystrophy
Lipodystrphy Dunnigan typeLMNA Lamin C Prelamin ALMNB1 Lamin B1LMNB2 Lamin B2OMIM_601487OMIM_x600937Pelger Huet anomalyPersistent hyperinsulinemic hypoglycemia of infancyPersistent neonatal hypoglycemiaRabson Mendenhall s syndromeReceptor (Insulin)Receptor (PPAR gamma)
SLC19A2 THTR1TNDM29locusWerner s syndromeWfs1 WolframinWfs2Wolcott Rallison syndromeWolfram s syndrome DIDMOADWRN
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All Medline data shown were primarily retrieved from MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.