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| Term | TNF receptor–associated periodic syndrome | ID (Ontology) | DOID:0090018 (Human Disease) |
| Definition | An autoinflammatory disease characterized by recurrent fever, abdominal pain, localized tender skin lesions, arthralgia and myalgia associated with skin, joint, ocular and serosal inflammation that has_material_basis_in heterozygous mutation in the TNFRSF1A gene on chromosome 12p13. | ||
| Also Known As | "autosomal dominant familial periodic fever" ; "familial Hibernian fever" ; "FHF" (for all, see Synonyms field below) | ||
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autosomal genetic disease |__autosomal dominant disease____ primary immunodeficiency disease | |__autoinflammatory disease______| TNF receptor–associated periodic syndrome |
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| Is a |
autosomal dominant disease autoinflammatory disease |
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GARD:8457 ICD10CM:E85.0 MIM:142680 ORDO:32960 |
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