arterioveneuze malformatie van cerebrale vaten	autosomaal dominante hereditaire aandoening	hereditaire aandoening van cardiovasculair systeem	hereditaire ontwikkelingsstoornis	lymfoedeem van onderste extremiteit	oedeem van voet	voetaandoening
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syndroom van lymfoedeem en cerebrale arterioveneuze malformatie (aandoening)
	syndroom van lymfoedeem en cerebrale arterioveneuze malformatie
	Lymphedema and cerebral arteriovenous anomaly syndrome
	This syndrome is characterized by the variable association of a cerebrovascular malformation, foot lymphedema and primary pulmonary hypertension. It has been described in a woman and four of her children.

Id	721979005
Status	Primitive

Associated morphology	lymfoedeem
Finding site	structuur van voet

Associated morphology	arterioveneuze malformatie
Finding site	structuur van intracraniële vasculatuur
Occurrence	congenitaal
Pathological process	proces van pathologische ontwikkeling

DHD Diagnosis thesaurus reference set

RIVM authorized national diagnosis thesaurus to ICD10 complex mapping reference set

Target	Q28.2
Term	Arterioveneuze malformatie van cerebrale vaten

Target	Q82.0
Term	Hereditair lymfoedeem

SNOMED CT to Orphanet simple map

86914

SNOMED CT to ICD-10 extended map

Target	Q28.2
Rule	TRUE
Advice	ALWAYS Q28.2 \| POSSIBLE REQUIREMENT FOR ADDITIONAL CODE TO FULLY DESCRIBE DISEASE OR CONDITION
Correlation	SNOMED CT source code to target map code correlation not specified

Target	Q82.0
Rule	TRUE
Advice	ALWAYS Q82.0
Correlation	SNOMED CT source code to target map code correlation not specified