dilated cardiomyopathy 1J
MeSH: C565337ORPHA: 217622
Overview
dilated cardiomyopathy that has material basis in mutation in the EYA4 gene on chromosome 6q23.2
Available Treatments (0)
No treatments linked yet
Clinical trials or compassionate use may be available — consult a specialist.
Clinical Presentation
Signs and symptoms associated with dilated cardiomyopathy 1J, sourced from HPO and Orphanet clinical annotations.
Hearing impairmentRecurrent otitis mediaCongestive heart failureDilated cardiomyopathyAbnormal cardiac ventricular function
Classification & Codes
MeSH Code
C565337Orphanet Code
ORPHA:217622dilated cardiomyopathy 1J
| MeSH | C565337 |
| Orphanet | ORPHA:217622 |
| Treatments | 0 drug(s) |
| Symptoms on record | 5 signs |
| Status | published |
Factual Authority
Last Updated3/20/2026
Clinical DataHPO · Orphanet
Drug DataFDA · EMA · CDSCO