autosomal dominant familial periodic fever
Go to external page http://purl.obolibrary.org/obo/MONDO_0007727
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. [ Orphanet:32960 https://orcid.org/0000-0001-5208-3432 ]
Synonyms: TRAPS tumour necrosis factor receptor 1 associated periodic syndrome FHF TNF receptor 1-associated periodic syndrome TNF receptor-associated periodic fever syndrome Tumor Necrosis Factor Receptor-Associated Periodic Syndrome TNF receptor-associated periodic syndrome familial Hibernian fever tumour necrosis factor receptor 1-associated periodic syndrome Hibernian fever, familial tumor necrosis factor receptor 1 associated periodic syndrome tumour necrosis factor receptor-associated periodic syndrome TRAPS syndrome tumor necrosis factor receptor 1-associated periodic syndrome tumor necrosis factor receptor-associated periodic syndrome
Term information
- SCTID:403833009 (MONDO:equivalentTo)
- MEDGEN:226899 (MONDO:equivalentTo)
- NANDO:2200433 (https://orcid.org/0000-0003-0011-764X)
- DOID:0090018 (MONDO:equivalentTo)
- OMIM:142680 (Orphanet:32960/e)
- NANDO:1200472 (https://orcid.org/0000-0003-0011-764X)
- Orphanet:32960 (OMIM:142680)
- MESH:C536657 (MONDO:equivalentTo)
- GARD:8457 (MONDO:GARD)
- icd11.foundation:1869883509 (https://orcid.org/0000-0001-5208-3432)
- NORD:1804 (MONDO:NORD)
- UMLS:C1275126 (MONDO:equivalentTo)
- NCIT:C119051 (MONDO:equivalentTo)
gard_rare, ordo_disorder, otar, rare, nord_rare, orphanet_rare
http://identifiers.org/mesh/C536657
http://linkedlifedata.com/resource/umls/id/C1275126
https://omim.org/entry/142680
http://www.orpha.net/ORDO/Orphanet_32960
http://purl.obolibrary.org/obo/DOID_0090018
http://identifiers.org/snomedct/403833009
http://purl.obolibrary.org/obo/NCIT_C119051
http://identifiers.org/medgen/226899