MSeqDR Mitochondrial Disease Portal


 
*:HP: HPO terms, ND: NAMDC terms.
  Most Studied  CPEO, Complex I Deficiency, COXPD1, Leigh, LHON, MELAS, MERRF, NARP, SANDO
Disease Browser
Parent Node:
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disease of macromolecular complex (MONDO:0044971)
Parent Node:
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rheumatologic disorder (MONDO:0005554)
..Starting node
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autoinflammatory syndrome ()

       Child Nodes:
........expandadult-onset Still disease ()
........expandautoinflammatory syndrome with immune deficiency ()
........expandautoinflammatory syndrome with skin involvement ()
........expandgranulomatous autoinflammatory syndrome ()
........expandmixed autoinflammatory and autoimmune syndrome ()
........expandperiodic fever syndrome ()
........expandpyogenic autoinflammatory syndrome ()
........expandsystemic-onset juvenile idiopathic arthritis ()
........expandtype 1 interferonopathy ()
........expandunclassified autoinflammatory syndrome ()



 Sister Nodes: 
..expandacroosteolysis dominant type ()
..expandarthritis ()
..expandautoinflammatory syndrome ()
..expandcamptodactyly-arthropathy-coxa vara-pericarditis syndrome ()
..expandfibroblastic rheumatism ()
..expandGorham-Stout disease ()
..expandidiopathic juvenile osteoporosis ()
..expandimmune dysregulation-inflammatory bowel disease-arthritis-recurrent infections syndrome ()
..expandintermittent hydrarthrosis ()
..expandinterstitial granulomatous dermatitis with arthritis ()
..expandisolated sternocostoclavicular hyperostosis ()
..expandlupus erythematosus ()
..expandmixed connective tissue disease ()
..expandpalindromic rheumatism ()
..expandpolymyalgia rheumatica ()
..expandprogeria-associated arthropathy ()
..expandrheumatic disease of mitral valve ()
..expandrheumatic pulmonary valve disease ()
..expandscleroderma (disease) ()
..expandsweet syndrome ()
   

MONDO is developed by the Monarch Initiative. Human Disease MESH is developed by UMLS.
Further data from MedGen, OMIM,ClinVar, CTD
Term ID:19751
Name:autoinflammatory syndrome
Definition:A group of disorders of the innate immune system characterized by attacks of seemingly unprovoked inflammation without significant levels of either autoantibodies or autoreactive T cells more characteristic of autoimmune disease.
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Reference: MedGen:
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MSeqDR LSDB:  
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MSeqDR Portal