ABCC8 SUR1Anemia (megaloblastic thiamine responsive)Ataxia teleangiectasiaBererdinelli Seip congenital lipodystrophyBloom s syndromeBSCL1 AGPAT2BSCL2 SeipinCell cylce (BASKET)Cockayne s syndromeDiabetes mellitus (Hereditary MODY)Diabetes mellitus (hereditary)Diabetes mellitus (neonatal)
DNA (helicase)Donohue s syndrome LeprechaunismEIF2AK3 PERKFRDA1 FrataxinFriedreich ataxiaGenetic instabilityGlucokinaseGLUD1Hutchinson Gilford syndromeInsulin resistance type aKCNJ11 Kir6 2Lipodystrophy
OMIM_601487OMIM_x600937Persistent hyperinsulinemic hypoglycemia of infancyPersistent neonatal hypoglycemiaProgeriaRabson Mendenhall s syndromeReceptor (Insulin)Receptor (PPAR gamma)RecQRothmund Thomson s syndromeSLC19A2 THTR1Telomere
TNDM29locusTrichothiodystrophyWerner s syndromeWfs1 WolframinWfs2Wolcott Rallison syndromeWolfram s syndrome DIDMOADWRNXeroderma pigmentosum
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All Medline data shown were primarily retrieved from MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.