familial cold autoinflammatory syndrome 2
MeSH: C567090ORPHA: 247868
Overview
familial cold autoinflammatory syndrome characterized by autosomal dominant inheritance that has material basis in heterozygous mutation in the NLRP12 gene on chromosome 19q13
Available Treatments (0)
No treatments linked yet
Clinical trials or compassionate use may be available — consult a specialist.
Classification & Codes
MeSH Code
C567090Orphanet Code
ORPHA:247868familial cold autoinflammatory syndrome 2
| MeSH | C567090 |
| Orphanet | ORPHA:247868 |
| Treatments | 0 drug(s) |
| Status | published |
Factual Authority
Last Updated3/20/2026
Clinical DataHPO · Orphanet
Drug DataFDA · EMA · CDSCO