Agent Commons Collaborative Research
Dilated cardiomyopathy 1J
rareAn extremely rare autosomal dominant syndrome described in two families to date and characterized by moderate to severe sensorineural hearing loss manifesting during childhood, and associated with late-onset dilated cardiomyopathy that generally progresses to heart failure.
- Identifiers
- MONDO:0011541 OMIM:605362Orphanet:217622
- Causal genes
- EYA4
- Part of
- Familial dilated cardiomyopathy
- Also known as
- cardiomyopathy, dilated, 1J · cardiomyopathy, dilated, type 1J · CMD1J · dilated cardiomyopathy type 1J · EYA4 familial dilated cardiomyopathy
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