autosomal dominant familial periodic fever

human disease
rdfs:label
"autosomal dominant familial periodic fever"@en
skos:altLabel
"Fpf"@en
"Hibernian Fever, Familial"@en
"PERIODIC FEVER, FAMILIAL, AUTOSOMAL DOMINANT"@en
"TNF receptor 1-associated periodic syndrome"@en
"TNF receptor-associated periodic syndrome"@en
"TRAPS"@en
"TRAPS syndrome"@en
"Tnf Receptor-Associated Periodic Syndrome"@en
"Tumor Necrosis Factor Receptor 1-Associated Periodic Syndrome"@en
"Tumor Necrosis Factor Receptor-Associated Periodic Syndrome"@en
"familial hibernian fever"@en
"tumor necrosis factor receptor 1 associated periodic syndrome"@en
schema:description
"human disease"@en
schema:dateModified "2026-10-24T00:08:02+00:00"^^xsd:dateTime
schema:version 2560162772
wikibase:identifiers 15
17
wikibase:sitelinks 6
wikibase:statements 53
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p:direct-normalized/P4527 <http://data.parliament.uk/terms/435874>
p:direct-normalized/P486 <http://id.nlm.nih.gov/mesh/C536657>
p:direct-normalized/P5270 <http://purl.obolibrary.org/obo/MONDO_0007727>
p:direct-normalized/P6366 <https://makg.org/entity/2778432415>
p:direct-normalized/P665 <http://www.kegg.jp/entry/H00912>
p:direct-normalized/P699 <http://purl.obolibrary.org/obo/DOID_DOID:0090018>
wdt:P11143 "TNF receptor associated periodic syndrome"
wdt:P11430 "DI-00491"
wdt:P1325 <http://www.nanbyou.or.jp/entry/4033>
wdt:P14914 "D32960"
wdt:P1550 "32960"
wdt:P1748 "C119051"
wdt:P1995 immunology
wdt:P2293 TNFRSF1A
wdt:P279 autosomal dominant disease
autoinflammatory syndrome with immune deficiency
autoinflammatory syndrome with skin involvement
hereditary periodic fever syndrome
autoimmune disease
wdt:P2841 infantile onset
childhood onset
juvenile onset
adult onset
wdt:P2888 <http://identifiers.org/doid/DOID:0090018>
<http://purl.obolibrary.org/obo/DOID_0090018>
<http://www.orpha.net/ORDO/Orphanet_32960>
wdt:P2892 "C1275126"
wdt:P31 type of disease
designated intractable/rare disease
rare disease
wdt:P4229 "E85.0"
wdt:P4233 "familial-hibernian-fever"
wdt:P4317 "8457"
wdt:P4527 "435874"
wdt:P486 "C536657"
wdt:P492 "142680"
wdt:P5008 WikiProject Medicine
wdt:P5270 "MONDO_0007727"
wdt:P6366 "2778432415"
wdt:P6532 splenomegaly
erythema
ecchymosis
migraine
Hypermelanotic macule
Abnormal sacroiliac joint morphology
bowel obstruction
cranial nerve palsy
fasciitis
uveitis
behavioral abnormality
pericarditis
vasculitis
chest pain
cellulitis
leukocytosis
wdt:P665 "H00912"
wdt:P699 "DOID:0090018"
wdt:P7464 "tumor-necrosis-factor-receptor-associated-periodic-syndrome"
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