CIM11 EC20.00

Ichthyosis vulgaris

chapitre: 14 Diseases of the skin
bloc: Genetic or developmental disorders affecting the skin
definition: Ichthyosis vulgaris accounts for 95% of all cases of hereditary ichthyosis. It is an autosomal dominant condition due to filaggrin gene mutations. At birth the skin may appear normal but it gradually becomes dry, rough and scaly, with most signs and symptoms appearing by the age of 5. Ichthyosis vul
type: category
navigateur oms (fr): https://icd.who.int/browse/2026-01/mms/fr#841161884 ↗