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syndroom van verdikte oorlellen en conductief gehoorverlies (aandoening)
syndroom van verdikte oorlellen en conductief gehoorverlies
syndroom van Escher-Hirt
syndroom van verdikte oorlellen en geleidingsgehoorverlies
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
Interpretsgehoorfunctie
Associated morphologyhypoplasie
Finding sitebotstructuur van mandibula
Occurrencecongenitaal
Pathological processproces van pathologische ontwikkeling
DHD Diagnosis thesaurus reference set
RIVM authorized national diagnosis thesaurus to ICD10 complex mapping reference set
TargetH90.0
TermGehoorverlies door geleidingsstoornis, dubbelzijdig
SNOMED CT to Orphanet simple map2405
SNOMED CT to ICD-10 extended map
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