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Mitochondrial myopathyMitochondriopathyMerrf syndromeGenetic disorderMetabolic bone diseaseInborn errors of metabolismCongenital myasthenic syndromeMelas syndromeCardiomyopathyPyruvate dehydrogenase deficiencyMyotonic dystrophyDiseaseEnzymopathyAdrenoleukodystrophyMotor neuron diseaseSickle cell diseaseHemoglobinopathyNephronophthisisHistidinemiaMyocardiodystrophyFanconi anemiaGaucher's diseaseChromosomal deletion syndromeAdenosine deaminase deficiencyAlagille syndromeThalassemiaCiliopathyDemyelinating diseaseMotor neurone diseaseSynucleinopathyDystrophinopathyMetachromatic leukodystrophyMuscular dystrophyImmune disorderAutoimmune diseaseRefsum's diseaseHypogranulocytosisMetabolic disorderAdermatoglyphiaNeurological disorderDysautonomiaThyroid diseaseChondrodystrophyMelasDiastrophic dysplasiaOmenn syndromeMyelopathyAntisynthetase syndromeSphingolipidosisEndocardiosisMyeloradiculopathyDysmetabolismNeuronopathyGangliosidosisOsteochondrodysplasiaSulfatidosisHuntington's diseaseSarcoglycanopathyCongenital adrenal hyperplasiaMethylmalonic acidemiaLipodystrophyLeukodystrophyAmyloidosisHunter syndromeNiemann-pick diseaseMyopathyBone diseaseNeuromuscular diseaseNeurosarcoidosisMcardle's diseaseCystinosisFabry diseaseDysmyelopoiesisFamilial mediterranean feverRasopathyLeukoencephalomyelopathyNeurodegenerative diseaseCerebellar ataxiaCauses of cancerDysbiosisLeigh diseaseMicrocytosisSickle-cell diseaseOrgan dysfunctionAlpha-1 antitrypsin deficiencyAngelman syndromeKetoacidemiaCauses of parkinson's diseaseCharge syndromeAutistic spectrum disorderPycnodysostosisMyotonia congenitaCytopathyMyositisHypochondrodysplasiaDesmosterolosisMccune-albright syndromeDentinogenesis imperfectaAlymphocytosisMotor disorder