You are using an outdated browser. Please upgrade your browser to improve your experience.
autosomal dominant ichthyosis vulgaris
Disease Summary
Associated Targets (1)
Tbio
1
Mondo Description Ichthyosis vulgaris is a common skin disorder passed down through families that leads to dry, scaly skin. It often begins in early childhood. Treatment may include heavy duty moisturizers which contain chemicals that help the skin to shed normally, including lactic acid, salicylic acid, and urea. Ichthyosis vulgaris can be a nuisance, but it rarely affects overall health. The condition usually disappears during adulthood, but may return in later years. This condition is inherited in an autosomal dominant pattern.
Disease Ontology Description An ichthyosis that has_material_basis_in heterozygous mutation in the filaggrin gene on chromosome 1q21 and is characterized by dead skin cells accumulate in thick, dry scales on your skin's surface.
Download Data for autosomal dominant ichthyosis vulgaris
data still loading...
Counts of Target Development Levels for diseases known to be associated with this disease. If the disease has a valid DOID, targets known to be associated with all child diseases are aggregated. Click "Explore Associated Targets" to view more facets and details for the target list.
Description from Mondo Disease Ontology.
Description from Disease Ontology
DataSources which have contributed target associations to this disease, and the identifiers by which the disease is referenced.
DOID:1702
GARD:0001897
ICD10:Q80.0
MESH:D016112
OMIM:146700
SCTID:254157005
UMLS:C0079584
MONDO:0007810
High level summary of knowledge for a disease, including descriptions and datasource references.