ichthyosis vulgaris (DOID:1702)
Alliance: disease page
Synonyms: Dominant congenital ichthyosiform erythroderma
Alt IDs: OMIM:146700, ICD10CM:Q80.0, MESH:D016112, NCI:C84778, UMLS_CUI:C0079584
Definition: An ichthyosis that has_material_basis_in heterozygous mutation in the filaggrin gene (FLG) on chromosome 1q21 and is characterized by dead skin cells accumulate in thick, dry scales on your skin's surface.