Autosomal dominant hereditary disorder
Retinitis pigmentosa
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Autosomal dominant retinitis pigmentosa (disorder)
Autosomal dominant retinitis pigmentosa
autosomaal dominante retinitis pigmentosa
autosomaal dominante aandoening van fotoreceptoren en pigmentepitheel van netvlies
autosomaal dominante TRD
autosomaal dominante tapedoretinale degeneratie
Id232052009
StatusDefined
Associated morphologyDystrophy
Finding siteRetinal structure
ICD-10 complex map reference set
TargetH35.5
RuleTRUE
AdviceALWAYS H35.5
CorrelationSNOMED CT source code to target map code correlation not specified
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Osteochondrodysplatic nanism, deafness, retinitis pigmentosa syndrome