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Congenital myasthenic syndromeSpinal muscular atrophiesMotor neuron diseaseMuscular dystrophyMitochondrial myopathyMyotonia congenitaNeurofibromatosisFocal cortical dysplasiaCentral pontine myelinolysisPolymyositisNeuromuscular diseaseRadiculopathyLeigh syndromeMyositis ossificansAdenomyosisLateral medullary syndromeNeuroferritinopathyNeurosarcoidosisMyopathyBasal ganglia diseaseDiastematomyeliaMerrf syndromeNiemann-pick diseaseCentral nervous system diseaseMyosclerosisMyotonic dystrophyPorencephalyFibromuscular dysplasiaSteatocystoma multiplexRefsum's diseasePlasmacytomaTethered spinal cord syndromeCerebellar degenerationParamyotonia congenitaLower motor neuron lesionPentalogy of cantrellMeningomyeloceleNeuromyotoniaMcleod syndromeMicropolygyriaProteus syndromeMyelodysplastic syndromePhakomatosisMastocytosisRhabdomyosarcomaCastleman diseaseMelorheostosisCephalic disorderErdheim-chester diseaseMitochondriopathyLipodystrophyCerebellopontine angle syndromeCardiac amyloidosisMyelomeningoceleSpastic hemiplegiaFibrous dysplasia of boneCurrarino syndromeEncephaloceleMitochondrial diseaseAminoacidopathyCerebral palsyAlexander diseaseGlycogen storage disease type iiGliomatosis cerebriCritical illness polyneuropathyCongenital heart defectIon channelopathyGerstmann syndromeCamurati-engelmann diseaseMeckel-gruber syndromeTumefactive multiple sclerosisNeurofibromatosis type iiPleurothotonusMedullary sponge kidneyGray matter heterotopia3c syndromeChondrodystrophyCancer syndromeArachnoiditisEnchondromatosisProgressive muscular atrophyHistiocytosisMyotoniaSatellitosisMyelitisFamilial multiple lipomatosisArthrogryposisSitus ambiguusDiffuse neonatal hemangiomatosisCongenital vertebral anomalyMyelodysplasiaMyofibromatosisMyelophthisisSpinal disc herniationCiliopathyInborn errors of metabolismHereditary elliptocytosisCauda equina syndromePyruvate dehydrogenase deficiencyPseudomeningocele