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infantiele neuronale ceroïdlipofuscinose (aandoening)
infantiele neuronale ceroïdlipofuscinose
ziekte van Santavuori-Hagberg
NCL-1
ziekte van Haltia-Santavuori
Dit is een vorm van neuronale ceroïdlipofuscinosen die begint voor het tweede levensjaar.
Infantile neuronal ceroid lipofuscinosis
Polyunsaturated acid lipidosis
Neuronal ceroid lipofuscinosis, infantile Finnish type
Neuronal ceroid lipofuscinosis infantile Finnish type
Haltia-Santavouri type neuronal ceroid lipofuscinosis
Polyunsaturated fatty acid lipidosis
Hagberg-Santavuori disease
Santavuori disease
Hagberg-Santavouri type neuronal ceroid lipofuscinosis
Id58258004
StatusPrimitive
Occurrencecongenitaal
Associated morphologydegeneratieve afwijking
DHD Diagnosis thesaurus reference set
RIVM authorized national diagnosis thesaurus to ICD10 complex mapping reference set
TargetE75.4
TermNeuronale ceroïde lipofuscinose
SNOMED CT to Orphanet simple map79263
SNOMED CT to ICD-10 extended map
TargetE75.4
RuleTRUE
AdviceALWAYS E75.4
CorrelationSNOMED CT source code to target map code correlation not specified
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