has material basis in germline mutation in TNFRSF1A immune system disorder autoimmune disease TNF receptor 1-associated periodic fever syndrome https://github.com/monarch-initiative/mondo/issues/6747 https://github.com/monarch-initiative/mondo/issues/7707 https://www.malacards.org/card/periodic_fever_familial_autosomal_dominant periodic FEVER, familial, autosomal dominant UMLS:C1275126 tumor necrosis factor receptor 1-associated periodic syndrome TNF receptor 1-associated periodic fever syndrome DOID:0090018 Hibernian fever, familial TRAPS OMIM:142680 familial Hibernian fever A periodic fever syndrome, characterized by recurrent fever, arthralgia, myalgia and tender skin lesions lasting for 1 to 3 weeks, associated with skin, joint, ocular and serosal inflammation and complicated by secondary amyloidosis. SCTID:403833009 MESH:C536657 tumor necrosis factor receptor-associated periodic syndrome icd11.foundation:1869883509 FPF NANDO:2200433 Tumor Necrosis Factor Receptor-Associated Periodic Syndrome tumour necrosis factor receptor 1 associated periodic syndrome tumour necrosis factor receptor 1-associated periodic syndrome NCIT:C119051 TRAPS syndrome NANDO:1200472 TNF receptor-associated periodic syndrome FHF Orphanet:32960 MONDO:0007727 NORD:1804 tumour necrosis factor receptor-associated periodic syndrome tumor necrosis factor receptor 1 associated periodic syndrome autosomal dominant familial periodic fever GARD:0008457 MEDGEN:226899 TNF receptor 1-associated periodic syndrome hereditary periodic fever syndrome