2 deoxyglucoseABCC8 SUR1Alloxanalpha MethylglucopyranosideAnemia (megaloblastic thiamine responsive)Beckwith Wiedemann syndromeBererdinelli Seip congenital lipodystrophyBSCL1 AGPAT2BSCL2 SeipinD glucosamineDiabetes mellitus (Hereditary MODY)Diabetes mellitus (hereditary)Diabetes mellitus (neonatal)
Donohue s syndrome LeprechaunismEIF2AK3 PERKEnzyme structure and chemistryFRDA1 FrataxinFriedreich ataxiaGlucokinaseGlucose (Hypoglycemia)Glucose (Sensing)GLUD1Glutamate dehydrogenaseHyperinsulinism in infancyInsulin resistance type aKATP
KCNJ11 Kir6 2LipodystrophyN acetyl D glucosamineOMIM_601487OMIM_x600937Perlman syndromePersistent hyperinsulinemic hypoglycemia of infancyPersistent neonatal hypoglycemiaPhloridzinRabson Mendenhall s syndromeReceptor (Insulin)Receptor (PPAR gamma)Short chain L 3 hydroxyacyl CoA dehydrogenase
SLC19A2 THTR1SLC5A1 SGLT1Sotos 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.