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

Id	21634003
Status	Primitive

Associated morphology	morfologische afwijking
Finding site	structuur van encephalon
Occurrence	congenitaal
Pathological process	proces van pathologische ontwikkeling

Has interpretation	gestoord
Interprets	intellectueel vermogen

Has interpretation	gestoord
Interprets	Adaptation behavior

Global Patient Set

DHD Diagnosis thesaurus reference set

SNOMED CT to Orphanet simple map

127

SNOMED CT to ICD-10 extended map

Target	Q87.8
Rule	TRUE
Advice	ALWAYS Q87.8 \| POSSIBLE REQUIREMENT FOR ADDITIONAL CODE TO FULLY DESCRIBE DISEASE OR CONDITION
Correlation	SNOMED CT source code to target map code correlation not specified