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syndroom van retinitis pigmentosa en doofheid type 3 (aandoening)
syndroom van retinitis pigmentosa en doofheid type 3
syndroom van Usher type 3
Usher-syndroom type 3
Retinitis pigmentosa-deafness syndrome type 3
Usher syndrome type 3
Id1010610007
StatusPrimitive
Associated morphologymorfologische afwijking
Occurrencecongenitaal
Pathological processproces van pathologische ontwikkeling
Interpretsgehoorfunctie
Associated morphologydystrofie
Finding sitestructuur van retina
referentieset met complexe 'mapping' naar ICD-10
TargetH35.5
RuleTRUE
AdviceALWAYS H35.5 | POSSIBLE REQUIREMENT FOR ADDITIONAL CODE TO FULLY DESCRIBE DISEASE OR CONDITION
CorrelationSNOMED CT source code to target map code correlation not specified