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Familial multiple fibrofolliculoma

ORPHA338
Synonym(s) -
Prevalence <1 / 1 000 000
Inheritance Autosomal dominant
Age of onset No data available
ICD-10 -
OMIM -
UMLS -
MeSH -
MedDRA -

Summary

Familial multiple fibrofolliculoma is a genodermatosis characterised by the presence of multiple hamartomas of the hair follicle. It has been described in one family so far.


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