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6 OMIM references -
2 associated genes
No signs/symptoms info
PROTEIN INTERACTIONS: 1
1 OMIM reference -
1 associated gene
No signs/symptoms info
Vitiligo-associated autoimmune disease
Primary systemic amyloidosis

FOXD3 APOA1
NLRP1


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
Primary systemic amyloidosis
APOA1



Vitiligo-associated autoimmune disease
Primary systemic amyloidosis

Synonym(s):
(no synonyms)

Synonym(s):
- Systemic AL amyloidosis
- Systemic immunoglobulinic amyloidosis

Classification (Orphanet):
- Rare skin disease
- Rare systemic or rheumatologic disease
Classification (Orphanet):
- Rare cardiac disease
- Rare genetic disease
- Rare hematologic disease
- Rare neurologic disease
- Rare oncologic disease
- Rare renal disease
- Rare systemic or rheumatologic 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:
1 OMIM reference -
No MeSH references

No signs/symptoms info available.