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NLRP12-associated hereditary periodic fever syndrome
1 OMIM reference -
1 associated gene
1 connected disease
No signs/symptoms info
Disease Type of connection
Pediatric systemic lupus erythematosus
- Familial cold autoinflammatory syndrome type 2
- NAPS12

Classification (Orphanet):
- Rare genetic disease
- Rare skin disease
- Rare systemic or rheumatologic disease

Classification (ICD10):
- Endocrine, nutritional and metabolic diseases -

Epidemiological data:
(no data available)
External references:
1 OMIM reference -
No MeSH references

Gene symbol UniProt reference OMIM reference
NLRP12 P59046609648
No signs/symptoms info available.