Click here to close Hello! We notice that you are using Internet Explorer, which is not supported by Xenbase and may cause the site to display incorrectly. We suggest using a current version of Chrome, FireFox, or Safari.
Summary Literature (0)
DOID:1702 - ichthyosis vulgaris

Disease Ontology 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.

Synonyms: Dominant congenital ichthyosiform erythroderma, Dominant congenital ichthyosiform erythroderma (disorder),

Xenbase Genes :

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0007810 - autosomal dominant ichthyosis vulgaris


Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s): autosomal dominant disease (is_a), ichthyosis (is_a)