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

C567090

Orphanet Code

ORPHA:247868
familial cold autoinflammatory syndrome 2
MeSHC567090
OrphanetORPHA:247868
Treatments0 drug(s)
Statuspublished
Factual Authority
Last Updated3/20/2026
Clinical DataHPO · Orphanet
Drug DataFDA · EMA · CDSCO