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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
CLOVE syndrome has characteristics of congenital lipomatous overgrowth, progressive, complex and mixed truncal vascular malformations and epidermal nevi. To date, less than 15 cases have been reported in the literature. Patients also present with disproportionate fat distribution. CLOVE syndrome may be associated with varying degrees of scoliosis and enlarged bony structures without progressive bony overgrowth. The presence of scoliosis/skeletal manifestations has led to the suggestion that the acronym CLOVE should be expanded to CLOVES.
Id719475006
StatusPrimitive
Associated morphologyepidermale naevus
Finding sitestructuur van huid
Occurrencecongenitaal
Associated morphologymorfologische afwijking
Finding sitestructuur van bloedvat
Occurrencecongenitaal
Pathological processproces van pathologische ontwikkeling
Associated morphologylipomateus neoplasma
Finding sitestructuur van weke delen
Occurrencecongenitaal
DHD Diagnosis thesaurus reference set
RIVM authorized national diagnosis thesaurus to ICD10 complex mapping reference set
TargetQ87.3
TermCongenitale gestoorde-ontwikkelingssyndromen met vroege versterkte groei
ICD-10 complex map reference set
TargetQ87.3
RuleTRUE
AdviceALWAYS Q87.3 | POSSIBLE REQUIREMENT FOR ADDITIONAL CODE TO FULLY DESCRIBE DISEASE OR CONDITION
CorrelationSNOMED CT source code to target map code correlation not specified