ichthyosis vulgaris

Summary
Synonym
  • Dominant congenital ichthyosiform erythroderma
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.
Super Class
autosomal dominant disease ichthyosis
External Links
Disease Ontology
DOID:1702
Mondo Disease Ontology
MeSH
UMLS
NCI Thesaurus
OMIM
GARD
MGI genotype (from TogoID)
Related Genes
Displaying all 2 entries
Gene ID Gene Symbol Description Source
242 ALOX12B arachidonate 12-lipoxygenase, 12R type
412 STS steroid sulfatase
Related Glycoprotein
Displaying all 2 entries
UniProt ID Protein Name Source
O75342 Arachidonate 12-lipoxygenase, 12R-type
P08842 Steryl-sulfatase

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Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

Partly supported by NIH Common Fund Grant #1U01GM125267-01


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Last updated: August 19, 2024