ichthyosis vulgaris
Information
- Disease name
- ichthyosis vulgaris
- Disease ID
- DOID:1702
- Description
- "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." [url:https\://www.mayoclinic.org/diseases-conditions/ichthyosis-vulgaris/symptoms-causes/syc-20373754]
Disease area statistics
[No Data.]
Chromosome band
[No Data.]
Annotation
| Genes | Mutation | Description | Source | Links |
|---|
| NCT ID | Status | Phase | Summary | Start date | Completion date |
|---|---|---|---|---|---|
| NCT01016106 | Completed | N/A | Genetic Screening for Filaggrin Mutation in Atopic Dermatitis and Ichthyosis Vulgaris in the African American Population | June 2010 | September 2011 |
| NCT03173547 | Completed | Phase 2 | A Six Week Topical Cream Study for Subjects With Ichthyosis Vulgaris | April 25, 2017 | July 31, 2019 |
| NCT00605878 | Recruiting | Studies of Skin Microbes in Healthy People and in People With Skin Conditions | January 22, 2008 | ||
| NCT02978209 | Unknown status | N/A | Comparison of Different Concentrations of Carbamide as Moisturizers in Ichthyosis Vulgaris | November 1, 2019 | March 31, 2020 |
| NCT04750161 | Unknown status | The Role Of Neutrophil Proteases As Global Regulators Of Il-1 Family Cytokine Activity In Skin Disorders | March 2, 2021 | June 2021 |
- Disase is a (Disease Ontology)
- DOID:1697
- Cross Reference ID (Disease Ontology)
- GARD:6752
- Cross Reference ID (Disease Ontology)
- ICD10CM:Q80.0
- Cross Reference ID (Disease Ontology)
- MESH:D016112
- Cross Reference ID (Disease Ontology)
- MIM:146700
- Cross Reference ID (Disease Ontology)
- NCI:C84778
- Cross Reference ID (Disease Ontology)
- SNOMEDCT_US_2023_03_01:205551004
- Cross Reference ID (Disease Ontology)
- UMLS_CUI:C0079584
- Exact Synonym (Disease Ontology)
- Dominant congenital ichthyosiform erythroderma
- MedGen concept unique identifier (MedGen Concept name)
- C0079584
- MedGen unique identifier (MedGen Concept name)
- 38217
- ICD10 preferred id (Insert disease from ICD10)
- D0014091
- ICD10 class code (Insert disease from ICD10)
- Q80.0
- MeSH unique ID (MeSH (Medical Subject Headings))
- D016112