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Vitiligo-associated autoimmune disease
6 OMIM references -
2 associated genes
9 connected diseases
No signs/symptoms info
Disease Type of connection
Corneal intraepithelial dyskeratosis with palmoplantar hyperkeratosis and laryngeal dyskeratosis
Follicular lymphoma
Intravascular large B-cell lymphoma
Apolipoprotein A-I deficiency
Familial renal amyloidosis due to Apolipoprotein AI variant
Primary systemic amyloidosis
Behçet disease
Blau syndrome
Pseudohypoaldosteronism type 2E
Synonym(s):
(no synonyms)
Classification (Orphanet):
- Rare skin disease
- Rare systemic or rheumatologic disease
Classification (ICD10):
(no data available)
Epidemiological data:
(no data available)
External references:
6 OMIM references -
No MeSH references
Gene symbol UniProt reference OMIM reference
FOXD3 Q9UJU5611539
NLRP1 Q9C000606636
No signs/symptoms info available.