Congenital lipomatous overgrowth, vascular malformation, epidermal nevi, skeletal anomaly syndrome (disorder) | | 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. | | syndroom van congenitale lipomateuze overgroei, vasculaire malformatie, epidermale naevi en skeletale anomalie | | CLOVE-syndroom CLOVES-syndroom 'congenital lipomatous overgrowth, vascular malformation, epidermal nevi, skeletal anomaly'-syndroom
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| Id | 719475006 | Status | Primitive |
DHD Diagnosis thesaurus reference set |
ICD-10 complex map reference set | 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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