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
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
2312 FLG filaggrin
3930 LBR lamin B receptor
Displaying 1 entry
Gene ID Gene Symbol Description Source
98386 Lbr lamin B receptor

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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: December 9, 2024