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Rombo syndrome (disorder)
Rombo syndrome
Rombo syndrome has characteristics of vermiculate atrophoderma, milia, hypotrichosis, trichoepitheliomas, and peripheral vasodilation with cyanosis and basal cell carcinomas. It has been described in four generations of one family and in two additional sporadic cases. The skin lesions become visible between 7 and 10 years of age and are most pronounced on the face. Basal cell carcinomas are frequent and develop at around 35 years of age.
Id721904001
StatusPrimitive
Associated morphologyverandering in groei
Finding sitestructuur van pilus
Associated morphologyatrophia
Finding sitestructuur van huid
ICD-10 complex map reference set
TargetL98.8
RuleTRUE
AdviceALWAYS L98.8 | POSSIBLE REQUIREMENT FOR ADDITIONAL CODE TO FULLY DESCRIBE DISEASE OR CONDITION
CorrelationSNOMED CT source code to target map code correlation not specified