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Progressive sensorineural hearing loss - hypertrophic cardiomyopathy
1 OMIM reference -
1 associated gene
28 connected diseases
No signs/symptoms info
Disease Type of connection
Autosomal dominant nonsyndromic sensorineural deafness type DFNA
Autosomal recessive nonsyndromic sensorineural deafness type DFNB
Amyotrophic lateral sclerosis
Familial cylindromatosis
Familial multiple trichoepithelioma
Anhidrotic ectodermal dysplasia - immunodeficiency - osteopetrosis - lymphedema
Hypohidrotic ectodermal dysplasia with immunodeficiency
Incontinentia pigmenti
Intermittent hydrarthrosis
TRAPS syndrome
X-linked mendelian susceptibility to mycobacterial diseases due to IKBKG deficiency
APC-related attenuated familial adenomatous polyposis
Catecholaminergic polymorphic ventricular tachycardia
Desmoid tumor
Estrogen resistance syndrome
Familial adenomatous polyposis due to 5q22.2 microdeletion
Gardner syndrome
Inflammatory myofibroblastic tumor
Translocation renal cell carcinoma
Turcot syndrome with polyposis
Young adult-onset Parkinsonism
X-linked non-syndromic intellectual deficit
Childhood-onset nemaline myopathy
Congenital fiber-type disproportion myopathy
Congenital myopathy with excess of thin filaments
Intermediate nemaline myopathy
Severe congenital nemaline myopathy
Typical nemaline myopathy
- Progressive neurosensory deafness - hypertrophic cardiomyopathy
- Progressive neurosensory hearing loss - hypertrophic cardiomyopathy
- Progressive sensorineural deafness - hypertrophic cardiomyopathy

Classification (Orphanet):
- Rare cardiac disease
- Rare developmental defect during embryogenesis
- Rare genetic disease
- Rare otorhinolaryngologic disease

Classification (ICD10):
(no data available)

Epidemiological data:
Class of prevalence: <1 / 1 000 000
Average age onset: variable
Average age of death: -
Type of inheritance: autosomal dominant
External references:
1 OMIM reference -
No MeSH references

Gene symbol UniProt reference OMIM reference
MYO6 Q9UM54600970
No signs/symptoms info available.