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Diseases
Genes (1037)
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SCN4A
Channelopathy
Hyperkalemic Periodic Paralysis
Potassium-Aggravated Myotonia
Hypokalemic Periodic Paralysis, Type 2
DSPP
Dentin Dysplasia Type Ii
Dentin Dysplasia
Dentinogenesis Imperfecta
SCN9A
Channelopathy
Paroxysmal Extreme Pain Disorder
Primary Erythromelalgia
GJA1
Oculodentodigital Dysplasia
Erythrokeratodermia Variabilis
KCNQ1
Channelopathy
Romano–ward Syndrome
Andersen–tawil Syndrome
ATP7A
Pectus Excavatum
Menkes Disease
BEST1
Vitelliform Macular Dystrophy
GJB2
Bartter Syndrome
Bart–pumphrey Syndrome
Clouston's Hidrotic Ectodermal Dysplasia
EFHC1
Epilepsy, Idiopathic Generalized, Susceptibility To, 9
GJB6
Clouston's Hidrotic Ectodermal Dysplasia
GJB3
Erythrokeratodermia Variabilis
ABCC9
Channelopathy
Cantú Syndrome
KCNJ2
Channelopathy
Hypokalemic Periodic Paralysis, Type 2
Andersen–tawil Syndrome
PTH1R
Failure Of Eruption Of Teeth
KCNC3
Spinocerebellar Ataxia Type-13
MAPT
Parkinson-Dementia Syndrome
CACNA1S
Channelopathy
Hypokalemic Periodic Paralysis, Type 2
Andersen–tawil Syndrome
COL27A1
Steel Syndrome
GABRA1
Epilepsy, Idiopathic Generalized, Susceptibility To, 9
KCNJ8
Cantú Syndrome