Defects in TNFRSF1A are a cause of autosomal dominant familial hibernian fever. Familial hibernian fever is a disease characterized by recurrent fever, abdominal pain, localized tender skin lesions and myalgia.
Alternative names
FHF, TRAPS, FPF
Familial hibernian fever
TNFR associated periodic syndrome
Classification
- Periodic fever syndromes
Inheritance
Autosomal dominant
Cross references
Phenotypically related immunodeficiencies
IDR factfile for Familial Mediterranean Fever
IDR factfile for Hyperimmunoglobulinemia D with periodic fever syndrome
Incidence
Incidence is not known.