aandoening van basale ganglia
autosomaal recessieve hereditaire aandoening
Congenital neurological disorder
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 basale ganglia
DHD Diagnosethesaurus-referentieset
referentieset met complexe 'mapping' naar ICD-10
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