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syndroom van verdikte oorlellen en geleidingsgehoorverlies (aandoening)
syndroom van verdikte oorlellen en geleidingsgehoorverlies
syndroom van Escher-Hirt
Thickened earlobe with conductive deafness syndrome
Escher Hirt syndrome
Syndrome with characteristics of microtia with thickened ear lobes, micrognathia and conductive hearing loss due to congenital ossicular anomalies. It has been described in two families. The mode of inheritance is autosomal dominant.
Id722476007
StatusPrimitive
Associated morphologyhypoplasie
Finding sitebotstructuur van mandibula
Occurrencecongenitaal
Pathological processproces van pathologische ontwikkeling
Interpretsgehoorfunctie
referentieset met complexe 'mapping' naar ICD-10
TargetH90.0
RuleTRUE
AdviceALWAYS H90.0 | POSSIBLE REQUIREMENT FOR ADDITIONAL CODE TO FULLY DESCRIBE DISEASE OR CONDITION
CorrelationSNOMED CT source code to target map code correlation not specified