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infantiele cerebellaire-retinale degeneratie (aandoening)
infantiele cerebellaire-retinale degeneratie
infantiele cerebellaire degeneratie en retinadegeneratie
mitochondriale aconitasedeficiƫntie
Infantile cerebellar and retinal degeneration
A rare, neurodegenerative disorder characterized by an early onset of truncal hypotonia, variable forms of seizures, athetosis, severe global developmental delay, intellectual disability and various ophthalmologic abnormalities, including strabismus, nystagmus, optic atrophy and retinal degeneration.
Id782822006
StatusPrimitive
Associated morphologydegeneratieve afwijking
Finding sitestructuur van retina
Occurrencezuigelingenperiode
Associated morphologyprimaire atrofie
Finding sitestructuur van nervus opticus
Occurrencezuigelingenperiode
DHD Diagnosis thesaurus reference set
RIVM authorized national diagnosis thesaurus to ICD10 complex mapping reference set
TargetE88.8
TermOverige gespecificeerde stofwisselingsstoornissen
SNOMED CT to Orphanet simple map313850
SNOMED CT to ICD-10 extended map
TargetE88.8
RuleTRUE
AdviceALWAYS E88.8 | POSSIBLE REQUIREMENT FOR ADDITIONAL CODE TO FULLY DESCRIBE DISEASE OR CONDITION
CorrelationSNOMED CT source code to target map code correlation not specified