Pages in category "Channelopathies" AAchromatopsiaAndersen–Tawil syndromeAutoimmune autonomic ganglionopathyAutosomal dominant nocturnal frontal lobe epilepsyAutosomal dominant polycystic kidney diseaseBBartter syndromeBenign familial neonatal seizuresBrugada syndromeCCalciumopathyCatecholaminergic polymorphic ventricular tachycardiaChannelomeChannelopathyChildhood absence epilepsyCongenital hyperinsulinismCongenital insensitivity to painCongenital stationary night blindnessCystic fibrosisDDent's diseaseEEpisodic ataxiaErythromelalgiaFFamilial atrial fibrillationFamilial hemiplegic migraineFocal segmental glomerulosclerosisGGeneralized epilepsy with febrile seizures plusHHemiplegic migraineHyperkalemic periodic paralysisHypokalemic periodic paralysisHypomagnesemia with secondary hypocalcemiaJJuvenile myoclonic epilepsyLLambert–Eaton myasthenic syndromeLong QT syndromeMMaculopathyMalignant hyperthermiaMucolipidosis type IVMyotonia congenitaNNonsyndromic deafnessPParamyotonia congenitaParoxysmal extreme pain disorderPeriodic paralysisPotassium-aggravated myotoniaPseudohypoaldosteronismRRetinitis pigmentosaRolandic epilepsyRomano–Ward syndromeSShort QT syndromeSpinocerebellar ataxia type 6Spinocerebellar ataxia type-13Sporadic hemiplegic migraineTTimothy syndrome