| 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. |
| | Id | 719475006 | | Status | Primitive |
| 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 |
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| 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 |
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