Usher-syndroom type 1
|
Usher-syndroom type 1F (aandoening)
Usher-syndroom type 1F
syndroom van retinitis pigmentosa en doofheid type 1F
syndroom van Usher type 1F
Usher syndrome type 1F
Id514793471000119104
StatusPrimitive
Interpretsgehoorfunctie
Associated morphologymorfologische afwijking
Occurrencecongenitaal
Pathological processproces van pathologische ontwikkeling
Finding sitestructuur van auditief systeem
Occurrencecongenitaal
Associated morphologydystrofie
Finding sitestructuur van retina
SNOMED CT to ICD-10 extended map
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
TargetH90.5
RuleTRUE
AdviceALWAYS H90.5
CorrelationSNOMED CT source code to target map code correlation not specified