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ADan-amyloïdose (aandoening)
ADan-amyloïdose
familiaire dementie Deens type
familiaire vorm van dementie Deens type
ADan amyloidosis
Familial dementia Danish type
A rare neurodegenerative disease with characteristics of progressive cataracts, hearing loss, cerebellar ataxia, paranoid psychosis and dementia. Neuropathological features are diffuse atrophy of all parts of the brain, chronic diffuse encephalopathy and the presence of extremely thin and almost completely demyelinated cranial nerves. Caused by mutation in the ITM2B gene.
Id783258000
StatusPrimitive
Associated morphologydepositie van amyloïd
Finding sitestructuur van encephalon
Has interpretationgestoord
Interpretscognitieve functie
Clinical courseprogressief
referentieset met complexe 'mapping' naar ICD-10
TargetE85.4
RuleTRUE
AdviceALWAYS E85.4 | POSSIBLE REQUIREMENT FOR ADDITIONAL CODE TO FULLY DESCRIBE DISEASE OR CONDITION
CorrelationSNOMED CT source code to target map code correlation not specified
TargetI68.0
RuleTRUE
AdviceALWAYS I68.0 | THIS CODE MAY BE USED IN THE PRIMARY POSITION WHEN THE MANIFESTATION IS THE PRIMARY FOCUS OF CARE
CorrelationSNOMED CT source code to target map code correlation not specified