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Disease Ontology Browser
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.

Disease References using Mouse Models (1)
Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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11/12/2024
MGI 6.24 		The Jackson Laboratory