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Non-syndromic genetic hearing loss (disorder)
Non-syndromic genetic hearing loss
Isolated genetic hearing loss
Non-syndromic genetic deafness
Isolated genetic deafness
Deafness is the most frequent form of sensorial deficit. In the vast majority of cases, the deafness is termed nonsyndromic or isolated and the hearing loss is the only clinical anomaly reported. In developed counties, 60-80% of cases of early-onset hearing loss are of genetic origin.
Id1260199008
StatusPrimitive
Has interpretationDecreased
InterpretsHearing
SNOMED CT to Orphanet simple map
SNOMED CT to ICD-10 extended map
TargetH90.5
RuleTRUE
AdviceALWAYS H90.5
CorrelationSNOMED CT source code to target map code correlation not specified
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