Auditory system hereditary disorder
Autosomal dominant hereditary disorder
Cardiovascular system hereditary disorder
Dilated cardiomyopathy
Hearing loss associated with syndrome
Sensorineural hearing loss
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Sensorineural deafness with dilated cardiomyopathy syndrome (disorder)
Sensorineural deafness with dilated cardiomyopathy syndrome
An extremely rare autosomal dominant syndrome described in two families to date and with characteristics of moderate to severe sensorineural hearing loss manifesting during childhood and associated with late-onset dilated cardiomyopathy that generally progresses to heart failure. Caused by mutation in the EYA4 gene.
syndroom van sensorineurale doofheid en dilaterende cardiomyopathie
syndroom van neurosensorisch gehoorverlies en gedilateerde cardiomyopathie
syndroom van perceptief gehoorverlies en gedilateerde cardiomyopathie
Id723993005
StatusPrimitive
InterpretsHearing
Associated morphologyDilatation
Finding siteMyocardium structure
Finding siteStructure of auditory system
DHD Diagnosis thesaurus reference set
ICD-10 complex map reference set
TargetH90.5
RuleTRUE
AdviceALWAYS H90.5
CorrelationSNOMED CT source code to target map code correlation not specified
TargetI42.0
RuleTRUE
AdviceALWAYS I42.0 | POSSIBLE REQUIREMENT FOR ADDITIONAL CODE TO FULLY DESCRIBE DISEASE OR CONDITION
CorrelationSNOMED CT source code to target map code correlation not specified