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Gene–disease association summaries
Gene–Disease Browser
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| Gene |
Disease |
Score |
Actions |
|
SCNN1A
(HGNC:10599)
|
Brugada syndrome
(MONDO_0015263)
|
Limited
|
|
|
SCN9A
(HGNC:10597)
|
epilepsy
(MONDO_0005027)
|
Refuted
|
|
|
SCN9A
(HGNC:10597)
|
channelopathy-associated congenital insensitivity to pain, autosomal recessive
(MONDO_0009459)
|
Strong
|
|
|
SCN9A
(HGNC:10597)
|
paroxysmal extreme pain disorder
(MONDO_0008179)
|
Definitive
|
|
|
SCN9A
(HGNC:10597)
|
primary erythermalgia
(MONDO_0007571)
|
Definitive
|
|
|
SCN8A
(HGNC:10596)
|
benign familial infantile epilepsy
(MONDO_0017615)
|
Moderate
|
|
|
SCN8A
(HGNC:10596)
|
developmental and epileptic encephalopathy, 13
(MONDO_0013801)
|
Strong
|
|
|
SCN8A
(HGNC:10596)
|
cognitive impairment with or without cerebellar ataxia
(MONDO_0013680)
|
Moderate
|
|
|
SCN5A
(HGNC:10593)
|
paroxysmal familial ventricular fibrillation
(MONDO_0100234)
|
Moderate
|
|
|
SCN5A
(HGNC:10593)
|
familial long QT syndrome
(MONDO_0019171)
|
Definitive
|
|
|
SCN5A
(HGNC:10593)
|
catecholaminergic polymorphic ventricular tachycardia
(MONDO_0017990)
|
Disputed
|
|
|
SCN5A
(HGNC:10593)
|
familial atrial fibrillation
(MONDO_0018054)
|
Moderate
|
|
|
SCN5A
(HGNC:10593)
|
arrhythmogenic right ventricular cardiomyopathy
(MONDO_0016587)
|
Limited
|
|
|
SCN5A
(HGNC:10593)
|
long QT syndrome 3
(MONDO_0011377)
|
Definitive
|
|
|
SCN5A
(HGNC:10593)
|
familial sick sinus syndrome
(MONDO_0012061)
|
Moderate
|
|
|
SCN5A
(HGNC:10593)
|
Brugada syndrome
(MONDO_0015263)
|
Definitive
|
|
|
SCN5A
(HGNC:10593)
|
atrial standstill
(MONDO_0015281)
|
Limited
|
|
|
SCN5A
(HGNC:10593)
|
progressive familial heart block, type 1A
(MONDO_0007240)
|
Moderate
|
|
|
SCN5A
(HGNC:10593)
|
dilated cardiomyopathy
(MONDO_0005021)
|
Moderate
|
|
|
SCN4A
(HGNC:10591)
|
myotonia permanens
(MONDO_0020482)
|
Moderate
|
|