aandoening van basale ganglia
autosomaal recessieve hereditaire aandoening
congenitale ziekte
hereditaire aandoening van zenuwstelsel
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biotine-responsieve basale ganglia-ziekte (aandoening)
biotine-responsieve basale ganglia-ziekte
Biotin-thiamine-responsive basal ganglia disease
Biotin-responsive basal ganglia disease
Thiamine metabolism dysfunction syndrome 2
Thiamine transporter-2 deficiency
Id703522009
StatusPrimitive
Occurrencecongenitaal
Finding sitestructuur van basaal ganglion
SNOMED CT to Orphanet simple map
RIVM authorized national diagnosis thesaurus to ICD10 complex mapping reference set
TargetG25.8
TermOverige gespecificeerde extrapiramidale aandoeningen en aandoeningen met abnormale bewegingen
SNOMED CT to ICD-10 extended map
TargetE88.8
RuleTRUE
AdviceALWAYS E88.8 | POSSIBLE REQUIREMENT FOR AN EXTERNAL CAUSE CODE
CorrelationSNOMED CT source code to target map code correlation not specified
TargetG25.8
RuleTRUE
AdviceALWAYS G25.8
CorrelationSNOMED CT source code to target map code correlation not specified