Term Name: ichthyosis vulgaris
Synonyms: Dominant congenital ichthyosiform erythroderma
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.
Ontology: Human Disease [DOID:1702]   ( DOID:1702 )

Relationships
is a type of: autosomal dominant disease ichthyosis