ABCC8 SUR1Anemia (megaloblastic thiamine responsive)Angelman s syndromeBeckwith Wiedemann syndromeBererdinelli Seip congenital lipodystrophyBSCL1 AGPAT2BSCL2 SeipinDiabetes mellitus (Hereditary MODY)Diabetes mellitus (hereditary)Diabetes mellitus (neonatal transient)Diabetes mellitus (neonatal)
Donohue s syndrome LeprechaunismEIF2AK3 PERKFRDA1 FrataxinFriedreich ataxiaGenetics (Imprinting)GlucokinaseGLUD1Insemination (Artificial)Insulin resistance type aIon channel (Potassium)KCNJ11 Kir6 2
LipodystrophyMaternal hypomethylation syndromeOMIM_601487OMIM_x600937Persistent hyperinsulinemic hypoglycemia of infancyPersistent neonatal hypoglycemiaPrader Willi syndromePTH (Pseudohypoparathyroidism)Rabson Mendenhall s syndromeReceptor (Insulin)Receptor (PPAR gamma)
Russell Silver s syndromeSLC19A2 THTR1TNDM29locusUniparental disomy of chromosome 14Werner 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.