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Vitiligo-associated autoimmune disease
6 OMIM references -
2 associated genes
No signs/symptoms info
PROTEIN INTERACTIONS: 1
Familial renal amyloidosis due to Apolipoprotein AI variant
1 associated gene
No signs/symptoms info
Vitiligo-associated autoimmune disease
Familial renal amyloidosis due to Apolipoprotein AI variant

FOXD3
(UniProt - OMIM)
 APOA1
(UniProt - OMIM)
NLRP1
(UniProt - OMIM)

INTERACTOME
ASSOCIATIONS
(click on a score value to see the evidence)
NLRP1
(0.72)
APOA1


Citations in the biomedical literature:


Vitiligo-associated autoimmune disease
FOXD3 NLRP1
Familial renal amyloidosis due to Apolipoprotein AI variant
APOA1



Vitiligo-associated autoimmune disease
Familial renal amyloidosis due to Apolipoprotein AI variant

Synonym(s):
(no synonyms)

Synonym(s):
- Apolipoprotein AI amyloidosis
- Familial amyloid nephropathy due to apolipoprotein AI variant
- Hereditary amyloid nephropathy due to apolipoprotein AI variant
- Hereditary renal amyloidosis due to apolipoprotein AI variant
Classification (Orphanet):
- Rare skin disease
- Rare systemic or rheumatologic disease
Classification (Orphanet):
- Rare genetic disease
- Rare renal disease
Classification (ICD10):
(no data available)
Classification (ICD10):
- Endocrine, nutritional and metabolic diseases -
Epidemiological data:
(no data available)
Epidemiological data:
(no data available)
External references:
6 OMIM references -
No MeSH references
External references:
No OMIM references
No MeSH references
No signs/symptoms info available.