ABCC8 SUR1Anemia (megaloblastic thiamine responsive)Beckwith Wiedemann syndromeBererdinelli Seip congenital lipodystrophyBSCL1 AGPAT2BSCL2 SeipinDiabetes mellitus (Hereditary MODY)Diabetes mellitus (hereditary)Diabetes mellitus (neonatal)Donohue s syndrome LeprechaunismEIF2AK3 PERK
FRDA1 FrataxinFriedreich ataxiaGlucokinaseGlucose (Hypoglycemia)GLUD1Glutamate dehydrogenaseHyperinsulinism in infancyIGF1Insulin (resistance)Insulin resistance type aKCNJ11 Kir6 2
LipodystrophyOMIM_601487OMIM_x600937Perlman syndromePersistent hyperinsulinemic hypoglycemia of infancyPersistent neonatal hypoglycemiaRabson Mendenhall s syndromeReceptor (IGF1)Receptor (Insulin)Receptor (PPAR gamma)Short chain L 3 hydroxyacyl CoA dehydrogenase
SLC19A2 THTR1Sotos s syndromeTNDM29locusWerner 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.