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Sensorineural deafness with dilated cardiomyopathy
1 OMIM reference -
1 associated gene
3 connected diseases
No signs/symptoms info
Disease Type of connection
Autosomal dominant nonsyndromic sensorineural deafness type DFNA
BOR syndrome
Branchio-otic syndrome
Synonym(s):
- Neurosensory deafness with dilated cardiomyopathy
- Neurosensory hearing loss with dilated cardiomyopathy
- Sensorineural hearing loss with dilated cardiomyopathy
Classification (Orphanet):
- Rare cardiac disease
- Rare genetic disease
Classification (ICD10):
(no data available)
Epidemiological data:
Class of prevalence: <1 / 1 000 000
Average age onset: adolescence / young
Average age of death: -
Type of inheritance: autosomal dominant
External references:
1 OMIM reference -
No MeSH references
Gene symbol UniProt reference OMIM reference
EYA4 O95677603550
No signs/symptoms info available.