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

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

COMMON
GENES 		NLRP1


Citations in the biomedical literature:


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



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

Classification (Orphanet):
- Rare eye disease
- Rare genetic disease
Classification (Orphanet):
- Rare skin disease
- Rare systemic or rheumatologic disease
Classification (ICD10):
(no data available)
Classification (ICD10):
(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
Epidemiological data:
(no data available)
External references:
1 OMIM reference -
No MeSH references
External references:
6 OMIM references -
No MeSH references
No signs/symptoms info available.