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Glycogen storage disease type vGlycogen storage disease type iiiGlycogen storage disease type iiGlycogen storage disease type iGlycogenosisMcardle's diseaseGaucher's diseaseMetabolic disorderHurler syndromeMucopolysaccharidosisTyrosinemia type iHunter syndromeMorquio syndromeLipoprotein lipase deficiencyDiabetesMetachromatic leukodystrophyMuscular dystrophyLysosomal acid lipase deficiencyPyruvate dehydrogenase deficiencyGalactosemiaMethylmalonic acidemiaAminoacidopathyProgressive muscular atrophySucrose intoleranceFanconi syndromeKetoacidemiaFarber diseaseAspartylglucosaminuriaOrganic acidemiaDiabetes mellitusSanfilippo syndromeFucosidosisWolman diseaseFavismSitosterolemiaAddison's diseaseAbetalipoproteinemiaLactic acidosisSandhoff diseaseLipodystrophyCreatine transporter defectInborn errors of metabolismMyotonic dystrophyCarnosinemiaTyrosinemiaType 3c diabetesHereditary haemochromatosisAlkaptonuriaNeuroferritinopathyEhlers-danlos syndromePhenylketonuriaHawkinsinuriaFructose malabsorptionPolymyositisNeuromuscular diseaseLaron syndromeGluten-related disordersHyperkalemic periodic paralysisCongenital myasthenic syndromeChronic liver diseaseNiemann-pick diseaseHypophosphatemiaKetoacidosisSarcoglycanopathyKrabbe diseaseInsulin resistanceHereditary fructose intoleranceDysthyroidismAdrenal insufficiencyHartnup diseaseSulfatidosisFumarase deficiencyHypophosphatasiaNon-alcoholic fatty liver diseaseZellweger syndromeCoeliac diseaseType 2 diabetesType 1 diabetesCirrhosisRefsum diseaseLesch-nyhan syndromeExocrine pancreatic insufficiencyLeigh syndromeGray platelet syndromeHashimoto's thyroiditisRenal tubular acidosisMyosclerosisSevere combined immunodeficiencyAutoimmune hepatitisFibromuscular dysplasiaIminoglycinuriaOsteomalaciaBartter syndromeChronic granulomatous diseaseBardet-biedl syndromeGilbert's syndromeChronic fatigue syndromeAlcoholic liver diseaseSarcosinemiaNephrogenic diabetes insipidus