congenitaal hamartoom van huid	congenitale afwijking van bewegingsapparaat	congenitale vaatmalformatie	epidermale naevus	lipomateus neoplasma	neoplasma van weke delen
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syndroom van congenitale lipomateuze overgroei, vasculaire malformatie, epidermale naevi en skeletale anomalie (aandoening)
	syndroom van congenitale lipomateuze overgroei, vasculaire malformatie, epidermale naevi en skeletale anomalie
	CLOVES-syndroom 'congenital lipomatous overgrowth, vascular malformation, epidermal nevi, skeletal anomaly'-syndroom CLOVE-syndroom
	CLOVE syndrome
	Congenital lipomatous overgrowth, vascular malformation, epidermal nevi, skeletal anomaly syndrome CLOVES syndrome
	A rare developmental defect during embryogenesis characterized by congenital lipomatous overgrowth, complex and progressive combined vascular malformations affecting the trunk, and epidermal nevi.

Id	719475006
Status	Primitive

Associated morphology	epidermale naevus
Finding site	structuur van huid
Occurrence	congenitaal

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

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

Associated morphology	lipomateus neoplasma
Finding site	structuur van weke delen
Occurrence	congenitaal

DHD Diagnosis thesaurus reference set

RIVM authorized national diagnosis thesaurus to ICD10 complex mapping reference set

Target	Q87.3
Term	Congenitale gestoorde-ontwikkelingssyndromen met vroege versterkte groei

SNOMED CT to Orphanet simple map

140944

SNOMED CT to ICD-10 extended map

Target	Q87.3
Rule	TRUE
Advice	ALWAYS Q87.3 \| POSSIBLE REQUIREMENT FOR ADDITIONAL CODE TO FULLY DESCRIBE DISEASE OR CONDITION
Correlation	SNOMED CT source code to target map code correlation not specified