|
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)
|
Limited
|
|
|
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)
|
Moderate
|
|
|
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)
|
Strong
|
|
|
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)
|
Strong
|
|
|
MYH7
(HGNC:7577)
|
congenital heart disease
(MONDO_0005453)
|
Limited
|
|
|
MYH7
(HGNC:7577)
|
hypertrophic cardiomyopathy
(MONDO_0005045)
|
Definitive
|
|
|
MYH6
(HGNC:7576)
|
hypertrophic cardiomyopathy
(MONDO_0005045)
|
Limited
|
|
|
MYH7
(HGNC:7577)
|
dilated cardiomyopathy
(MONDO_0005021)
|
Strong
|
|