General Information of Disease (ID: DISHKOLS)

Disease Name Autosomal dominant ichthyosis vulgaris
Synonyms ichthyosis vulgaris; ichthyosis simplex; dominant ichthyosis vulgaris; dominant congenital ichthyosiform erythroderma; autosomal dominant ichthyosis vulgaris; ichthyosis vulgaris, autosomal dominant
Definition
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 Hierarchy
DISTRF9L: Ichthyosis vulgaris
DIS3HIWD: Autosomal dominant disease
DISHKOLS: Autosomal dominant ichthyosis vulgaris
Disease Identifiers
MONDO ID
MONDO_0007810
UMLS CUI
C0432300
MedGen ID
609440
Orphanet ID
462
SNOMED CT ID
254158000

Molecular Interaction Atlas (MIA) of This Disease

Molecular Interaction Atlas (MIA)
This Disease Is Related to 1 DOT Molecule(s)
Gene Name DOT ID Evidence Level Mode of Inheritance REF
FLG OTE9QDV6 Definitive Semidominant [1]
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References

1 The Gene Curation Coalition: A global effort to harmonize gene-disease evidence resources. Genet Med. 2022 Aug;24(8):1732-1742. doi: 10.1016/j.gim.2022.04.017. Epub 2022 May 4.