Variant Synonymizer: Platform to identify mutations defined in different ways is available now!

VarSy

Over 2,000 gene–disease validation summaries are now available—no login required!

Browse Summaries

Stats

Total associations
6681
Unique genes
4239
Unique diseases
3297
Gene–disease association summaries
Back to Open Access Summaries

Gene–Disease Browser

Need updated, customized, evidence‑backed summaries? Get it from the leaders in AI‑powered, evidence‑backed summaries provider.
Contact us
Gene Disease Score Actions
MYL2
(HGNC:7583)
congenital fiber-type disproportion myopathy
(MONDO_0009711)
 Limited
MYL2
(HGNC:7583)
arrhythmogenic right ventricular cardiomyopathy
(MONDO_0016587)
 Disputed
MYO7A
(HGNC:7606)
Usher syndrome type 1B
(MONDO_0700087)
 Definitive
MYO7A
(HGNC:7606)
autosomal dominant nonsyndromic hearing loss 11
(MONDO_0011032)
 Strong
MYO7A
(HGNC:7606)
autosomal recessive nonsyndromic hearing loss 2
(MONDO_0010807)
 Strong
MYO7A
(HGNC:7606)
Usher syndrome type 2
(MONDO_0016484)
 Moderate
MYO5A
(HGNC:7602)
Griscelli syndrome type 1
(MONDO_0008962)
 Moderate
MYO6
(HGNC:7605)
autosomal dominant nonsyndromic hearing loss 22
(MONDO_0011660)
 Strong
MYO15A
(HGNC:7594)
autosomal recessive nonsyndromic hearing loss 3
(MONDO_0010860)
 Definitive
MYL2
(HGNC:7583)
dilated cardiomyopathy
(MONDO_0005021)
 Limited
MYL1
(HGNC:7582)
congenital myopathy
(MONDO_0019952)
 Limited
MYH9
(HGNC:7579)
macrothrombocytopenia and granulocyte inclusions with or without nephritis or sensorineural hearing loss
(MONDO_0015912)
 Definitive
MYH7
(HGNC:7577)
left ventricular noncompaction
(MONDO_0018901)
 Definitive
MYH7
(HGNC:7577)
arrhythmogenic right ventricular cardiomyopathy
(MONDO_0016587)
 Limited
MYH7
(HGNC:7577)
Ebstein anomaly
(MONDO_0009144)
 Moderate
MYH8
(HGNC:7578)
trismus-pseudocamptodactyly syndrome
(MONDO_0008016)
 Strong
MYH7
(HGNC:7577)
congenital myopathy 7A, myosin storage, autosomal dominant
(MONDO_0008409)
 Strong
MYH7
(HGNC:7577)
MYH7-related skeletal myopathy
(MONDO_0008050)
 Definitive
MYH7
(HGNC:7577)
congenital heart disease
(MONDO_0005453)
 Limited
MYH7
(HGNC:7577)
hypertrophic cardiomyopathy
(MONDO_0005045)
 Definitive
Showing 681–700 of 6681