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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systemic or rheumatic disease (MONDO:0020012)
..Starting node
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systemic disease ()

       Child 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 ()



 Sister Nodes: 
..expandgenetic systemic or rheumatologic disease ()
..expandnon-histaminic angioedema ()
..expandsystemic disease ()
..expandvasculitis ()
   

MONDO is developed by the Monarch Initiative. Human Disease MESH is developed by UMLS.
Further data from MedGen, OMIM,ClinVar, CTD
Term ID:15938
Name:systemic disease
Definition:A systemic disease is one that affects a number of organs and tissues, or affects the body as a whole.
Alternative IDs:
ParentIDs:
TreeNumbers:
Synonyms:multi-system disorder; multisystem disorder; rare systemic disease; systemic disorder
Slim Mappings:
Reference: MedGen:
MeSH:
OMIM:
MSeqDR LSDB:  
Genes:
Phenotypes
Disease Causing ClinVar Variants
MSeqDR Portal