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Hyperkalemic periodic paralysisBartter syndromeHypophosphatasiaGitelman syndromePyruvate dehydrogenase deficiencyFamilial dysautonomiaLiddle's syndromeMultiple system atrophyLafora diseaseThyrotoxic periodic paralysisParamyotonia congenitaSpinal muscular atrophyOpsoclonus myoclonus syndromeHypokalemiaCanavan diseaseSpinal and bulbar muscular atrophyHypophosphatemiaGlycogen storage disease type iiProgressive muscular atrophyMyotonic dystrophyAlexander diseaseFumarase deficiencyPrimary lateral sclerosisFamilial amyloid polyneuropathyMuscular dystrophyMyotonia congenitaGray platelet syndromeKetoacidemiaAtaxia telangiectasiaAcute intermittent porphyriaSanfilippo syndromeCongenital myasthenic syndromeCongestive heart failureGuillain-barré syndromeFriedreich's ataxiaHyperpipecolatemiaLambert-eaton myasthenic syndromeMcleod syndromeChédiak-higashi syndromeLeigh syndromeFatal familial insomniaBecker muscular dystrophyCamurati-engelmann diseaseRasmussen's encephalitisFatal insomniaShort qt syndromeKrabbe diseaseGoodpasture syndromeSupranuclear palsyAdams-stokes syndromeGlycogen storage disease type vPelizaeus-merzbacher diseaseAceruloplasminemiaFabry diseaseLandau-kleffner syndromePrimary ciliary dyskinesiaMethylmalonic acidemiaAtypical hemolytic uremic syndromeHistidinemiaBenedikt syndromeRefsum diseaseParkinsonismHeart failureFanconi anemiaStiff-person syndromeCritical illness polyneuropathyPolyradiculoneuropathyAcdcPoliomyelitisLysosomal acid lipase deficiencyGlycogen storage disease type iiiHaemophiliaIdiopathic postprandial syndromeFunctional neurologic disorderAtonic seizureMetachromatic leukodystrophyMenkes diseaseNeurogenic shockCalciphylaxisPalsyMeckel-gruber syndromeRamsay hunt syndrome type 1AlkaptonuriaSevere combined immunodeficiencyAspartylglucosaminuriaMelas syndromeChannelopathyMyasthenia gravisMotor neuron diseaseRotor syndromePseudopseudohypoparathyroidismGalactosemiaPleurothotonusHypomagnesemiaEssential tremorCrigler-najjar syndromeAcute flaccid myelitisHistotoxic hypoxiaParkinson's diseaseSyncope