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Periodic fever, familial, autosomal dominant MeSH Supplementary Concept Data 2024

MeSH Supplementary
Periodic fever, familial, autosomal dominant
Unique ID
RDF Unique Identifier
Entry Term(s)
Autosomal Dominant Familial Periodic Fever
Familial Hibernian fever
Hibernian Familial Fever
Hibernian fever, familial
TNF Receptor-associated Periodic Syndrome (TRAPS)
TNF receptor-associated periodic syndrome
Tumor necrosis factor receptor-associated periodic syndrome
Registry Number
Heading Mapped to
*Hereditary Autoinflammatory Diseases
An inherited condition characterized by recurrent episodes of FEVER; onset is typically in early childhood. Fevers usually persist for about three weeks, though they can be longer or shorter, and may not occur again for several weeks or several years. Other symptoms may include ABDOMINAL PAIN; MYALGIA; ARTHRALGIA; SKIN RASH and systemic INFLAMMATION; AMYLOIDOSIS may also occur in some cases. There is often no trigger, but episodes are sometimes preceded by infections, injury, or stress. Germline mutations in the TNFRSF1A gene have been identified. OMIM: 142680
Date of Entry
Revision Date
Periodic fever, familial, autosomal dominant Preferred
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