Stats

Total associations
6699
Unique genes
4252
Unique diseases
3300
Gene–disease association summaries
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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
Showing 4241–4260 of 6699