Cytoscape Web
Click node...

Vitiligo-associated autoimmune disease
6 OMIM references -
2 associated genes
No signs/symptoms info
COMMON GENES: 1
Corneal intraepithelial dyskeratosis with palmoplantar hyperkeratosis and laryngeal dyskeratosis
1 OMIM reference -
1 associated gene
No signs/symptoms info
Vitiligo-associated autoimmune disease
Corneal intraepithelial dyskeratosis with palmoplantar hyperkeratosis and laryngeal dyskeratosis

FOXD3
(UniProt - OMIM)
 NLRP1
(UniProt - OMIM)
NLRP1
(UniProt - OMIM)

COMMON
GENES 		NLRP1


Citations in the biomedical literature:


Vitiligo-associated autoimmune disease
FOXD3 NLRP1
Corneal intraepithelial dyskeratosis with palmoplantar hyperkeratosis and laryngeal dyskeratosis



Vitiligo-associated autoimmune disease
Corneal intraepithelial dyskeratosis with palmoplantar hyperkeratosis and laryngeal dyskeratosis

Classification (Orphanet):
- Rare skin disease
- Rare systemic or rheumatologic disease
Classification (Orphanet):
- Rare eye disease
- Rare genetic disease
Classification (ICD10):
(no data available)
Classification (ICD10):
(no data available)
Epidemiological data:
(no data available)
Epidemiological data:
Class of prevalence: <1 / 1 000 000
Average age onset: variable
Average age of death: -
Type of inheritance: autosomal dominant
External references:
6 OMIM references -
No MeSH references
External references:
1 OMIM reference -
No MeSH references
No signs/symptoms info available.