EULAR/PRINTO/PRES classification criteria for childhood-onset polyarteritis nodosa.
Source: Reference: Adapted from Ozen S, Pistorio A, Iusan SM, et al: EULAR/PRINTO/PRES criteria for Henoch-Schönlein purpura, childhood polyarteritis nodosa, childhood Wegener granulomatosis and childhood Takayasu arteritis: Ankara 2008. Part II. Final classification criteria, Ann Rheum Dis 69:798–806; 2010
Assessment of SpondyloArthritis International Society classification criteria for axial and peripheral spondyloarthritis.
Tel Hashomer criteria for the diagnosis of familial Mediterranean fever.
Diagnostic criteria for familial cold autoinflammatory syndrome (FCAS).
EULAR/PRINTO/PRES classification criteria for Henoch-Schönlein purpura (IgA vasculitis).
Clinical and laboratory features of hyper-IgD syndrome (mevalonate kinase deficiency), a periodic fever syndrome.
American College of Rheumatology 1990 classification criteria for hypersensitivity vasculitis (≥3 of 5 criteria: sensitivity 71.0%, specificity 83.9%).
Doctaverse is clinical decision support for qualified clinicians — it is not a medical device and not for patients or parents.
Every tool is suggestion-only. The calculators are deterministic and unit-tested and the AI never invents a dose, but outputs are not a substitute for your training, examination, local protocols, or primary guidelines. Content is provided “as is”, without warranty; verify every value before acting on it.