ABCC8 SUR1ABCC9 SUR2AABCC9 SUR2BAdrenergic atrial fibrillationAnemia (megaloblastic thiamine responsive)Beckwith Wiedemann syndromeBererdinelli Seip congenital lipodystrophyBSCL1 AGPAT2BSCL2 SeipinCongenital hyperinsulinismDEND syndromeDiabetes mellitus (Hereditary MODY)Diabetes mellitus (hereditary)
Diabetes mellitus (neonatal transient)Diabetes mellitus (neonatal)Donohue s syndrome LeprechaunismEIF2AK3 PERKFRDA1 FrataxinFriedreich ataxiaGlucokinaseGlucose (Hypoglycemia)GLUD1Glutamate dehydrogenaseHeart (Cardiomyopathy dilated)Hyperinsulinism in infancyInsulin resistance type a
Ion channel (Potassium)KATPKCNJ11 Kir6 2KCNJ8 Kir6 1LipodystrophyOMIM_601487OMIM_x600937Perlman syndromePersistent hyperinsulinemic hypoglycemia of infancyPersistent neonatal hypoglycemiaRabson Mendenhall s syndromeReceptor (Insulin)Receptor (PPAR gamma)
Short chain L 3 hydroxyacyl CoA dehydrogenaseSLC19A2 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.