Preferred Label : Flegel disease;
ICD-11 definition : Flegel disease is an inherited autosomal dominant disorder and is characterized by
the development in early adult life of a profusion of 2–3 mm diameter keratotic papules
with discrete irregular margins over the calves and the extensor surfaces of the ankles.
Irritation may be severe and response to any form of treatment is poor.;
ICD-11 synonym : Hyperkeratosis lenticularis perstans;
Origin ID : 932302493;
Automatic exact mappings (from CISMeF team)
Flegel disease is an inherited autosomal dominant disorder and is characterized by
the development in early adult life of a profusion of 2–3 mm diameter keratotic papules
with discrete irregular margins over the calves and the extensor surfaces of the ankles.
Irritation may be severe and response to any form of treatment is poor.
