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:
expandautoimmune disease (MONDO:0007179)
Parent Node:
expandsystemic disease (MONDO:0015938)
..Starting node
..expandsystemic autoimmune disease ()

       Child Nodes:
........expandautoimmune hemolytic anemia-autoimmune thrombocytopenia-primary immunodeficiency syndrome ()
........expandautoimmune interstitial lung disease-arthritis syndrome ()
........expandBlau syndrome ()
........expanddrug-induced lupus erythematosus ()
........expandfamilial chilblain lupus ()
........expandfamilial cold autoinflammatory syndrome 3 ()
........expandidiopathic inflammatory myopathy ()
........expandIgG4-related disease ()
........expandoverlapping connective tissue disease ()
........expandrelapsing polychondritis ()
........expandretinal vasculopathy with cerebral leukoencephalopathy and systemic manifestations ()
........expandReynolds syndrome ()
........expandSatoyoshi syndrome ()
........expandscleroderma (disease) ()
........expandsecondary neonatal autoimmune disease ()
........expandsimple cryoglobulinemia ()
........expandSjogren syndrome ()
........expandSneddon syndrome ()
........expandSTAT3-related early-onset multisystem autoimmune disease ()
........expandSusac syndrome ()
........expandsyndromic multisystem autoimmune disease due to Itch deficiency ()
........expandsystemic lupus erythematosus (disease) ()
........expandundifferentiated connective tissue syndrome ()



 Sister Nodes: 
..expandamyloidosis (disease) ()
..expandcalciphylaxis ()
..expandcapillary leak syndrome ()
..expandconnective tissue disorder due to lysyl hydroxylase-3 deficiency ()
..expandEhlers-Danlos syndrome ()
..expandhereditary hemorrhagic telangiectasia ()
..expandhypoplasminogenemia ()
..expandKikuchi-Fujimoto disease ()
..expandKimura disease ()
..expandLangerhans cell histiocytosis ()
..expandmacrophage activation syndrome ()
..expandmalignant atrophic papulosis ()
..expandMarfan and Marfan-related disorder ()
..expandmyalgia-eosinophilia syndrome associated with tryptophan ()
..expandnon-Langerhans cell histiocytosis ()
..expandpostorgasmic illness syndrome ()
..expandprogeroid and marfanoid aspect-lipodystrophy syndrome ()
..expandretinal ischemic syndrome-digestive tract small vessel hyalinosis-diffuse cerebral calcifications syndrome ()
..expandReye syndrome ()
..expandrheumatic fever ()
..expandsarcoidosis ()
..expandsystemic autoimmune disease ()
..expandsystemic disease with cataract ()
..expandsystemic disease with skin involvement ()
..expandsystemic diseases with anterior uveitis ()
..expandsystemic diseases with panuveitis ()
..expandsystemic diseases with posterior uveitis ()
..expandTAFRO syndrome ()
..expandtempi syndrome ()
..expandunexplained long-lasting fever/inflammatory syndrome ()
..expandX-linked reticulate pigmentary disorder ()
   

MONDO is developed by the Monarch Initiative. Human Disease MESH is developed by UMLS.
Further data from MedGen, OMIM,ClinVar, CTD
Term ID:15939
Name:systemic autoimmune disease
Definition:An autoimmune form of systemic disease.
Alternative IDs:
ParentIDs:
TreeNumbers:
Synonyms:autoimmune systemic disease
Slim Mappings:
Reference: MedGen:
MeSH:
OMIM:
MSeqDR LSDB:  
Genes:
Phenotypes
Disease Causing ClinVar Variants
MSeqDR Portal