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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:0007810 - autosomal dominant ichthyosis vulgaris |
Other Model Organisms: AGR, 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)