MSeqDR Mitochondrial Disease Portal


 
*:HP: HPO terms, ND: NAMDC terms.
  Most Studied  CPEO, Complex I Deficiency, COXPD1, Leigh, LHON, MELAS, MERRF, NARP, SANDO
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Parent Node:
expandsystemic disease (MONDO:0015938)
..Starting node
..expandsystemic diseases with panuveitis ()

       Child Nodes:
........expandBehcet disease ()
........expandBlau syndrome ()
........expandchronic granulomatous disease ()



 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:17261
Name:systemic diseases with panuveitis
Definition:
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Reference: MedGen:
MeSH:
OMIM:
MSeqDR LSDB:  
Genes:
Phenotypes
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