congenitale afwijking van hersenen
genetische verstandelijke beperking
hereditaire aandoening van zenuwstelsel
hereditaire ontwikkelingsstoornis
malformatiesyndroom met betrokkenheid van meerdere systemen
X-gebonden hereditaire recessieve aandoening
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Borjeson-Forssman-Lehmann-syndroom (aandoening)
Borjeson-Forssman-Lehmann-syndroom
BFLS
syndroom van Borjeson-Forssman-Lehmann
Borjeson-Forssman-Lehmann syndrome
Borjeson syndrome
Id21634003
StatusPrimitive
Associated morphologymorfologische afwijking
Finding sitestructuur van encephalon
Occurrencecongenitaal
Pathological processproces van pathologische ontwikkeling
Has interpretationgestoord
Interpretsintellectueel vermogen
Has interpretationgestoord
InterpretsAdaptation behavior
Global Patient Set
SNOMED CT to Orphanet simple map
SNOMED CT to ICD-10 extended map
TargetQ87.8
RuleTRUE
AdviceALWAYS Q87.8 | POSSIBLE REQUIREMENT FOR ADDITIONAL CODE TO FULLY DESCRIBE DISEASE OR CONDITION
CorrelationSNOMED CT source code to target map code correlation not specified