Search Ontology:
Human Disease

ichthyosis vulgaris

Term ID
DOID:1702
Synonyms
  • 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. https://www.mayoclinic.org/diseases-conditions/ichthyosis-vulgaris/symptoms-causes/syc-20373754
References
  • GARD:6752
  • ICD10CM:Q80.0
  • MESH:D016112
  • MIM:146700
  • NCI:C84778
  • SNOMEDCT_US_2023_03_01:205551004
  • UMLS_CUI:C0079584
Ontology
Human Disease   ( DOID:1702 )
Relationships
is a type of
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
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