autosomal dominant familial periodic fever
MeSH: C536657ORPHA: 32960
Overview
human disease
Available Treatments (0)
No treatments linked yet
Clinical trials or compassionate use may be available — consult a specialist.
Clinical Presentation
Signs and symptoms associated with autosomal dominant familial periodic fever, sourced from HPO and Orphanet clinical annotations.
ConjunctivitisUveitisAtypical behaviorBruising susceptibilitySkin rashHypermelanotic maculeErysipelasArthritisAbnormal myocardium morphologyPericarditisSplenomegalyRecurrent feverIncreased total leukocyte countVomitingDiarrheaConstipationAbdominal painMigrainePleuritisVertigoPeritonitisVasculitisLymphadenopathyArthralgiaMyalgiaParesthesiaElevated erythrocyte sedimentation rateIntestinal obstructionCranial nerve paralysisErythemaElevated circulating C-reactive protein concentrationMaculeFasciitisPeriorbital edemaMyositisCellulitisChest painRecurrent pharyngitisAbnormal sacroiliac joint morphologyOrchitis
Classification & Codes
MeSH Code
C536657Orphanet Code
ORPHA:32960autosomal dominant familial periodic fever
| MeSH | C536657 |
| Orphanet | ORPHA:32960 |
| Treatments | 0 drug(s) |
| Symptoms on record | 40 signs |
| Status | published |
Factual Authority
Last Updated3/20/2026
Clinical DataHPO · Orphanet
Drug DataFDA · EMA · CDSCO