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:
expand
disease or disorder (MONDO:0000001)
..Starting node
..expand
syndromic disease ()

       Child Nodes:
........expandAchard syndrome ()
........expandAchenbach syndrome ()
........expandacute chest syndrome ()
........expandacute coronary syndrome ()
........expandadult respiratory distress syndrome ()
........expandanterior spinal artery syndrome ()
........expandantiphospholipid syndrome ()
........expandautosomal dominant chondrodysplasia punctata ()
........expandBarre-Lieou syndrome ()
........expandbrachydactyly-nystagmus-cerebellar ataxia syndrome ()
........expandBrown-Sequard syndrome ()
........expandburning mouth syndrome ()
........expandCADASIL ()
........expandCapgras syndrome ()
........expandcapillary leak syndrome ()
........expandcarcinoid syndrome ()
........expandcauda equina syndrome ()
........expandcentral sleep apnea syndrome ()
........expandcleidocranial dysplasia ()
........expandcompartment syndrome ()
........expanddiffuse infiltrative lymphocytosis syndrome ()
........expanddry eye syndrome ()
........expandDuane retraction syndrome ()
........expanddumping syndrome ()
........expandempty sella syndrome ()
........expandeuthyroid sick syndrome ()
........expandFanconi syndrome ()
........expandFG syndrome ()
........expandfibrogenesis imperfecta ossium ()
........expandfibromyalgia ()
........expandFroelich syndrome ()
........expandFuchs' heterochromic uveitis ()
........expandGorham disease ()
........expandhepatorenal syndrome ()
........expandhypoplastic left heart syndrome ()
........expandinclusion body myopathy with Paget disease of bone and frontotemporal dementia ()
........expandirritable bowel syndrome ()
........expandKluver-Bucy syndrome ()
........expandlateral medullary syndrome ()
........expandlong QT syndrome ()
........expandLown-Ganong-Levine syndrome ()
........expandmedian arcuate ligament syndrome ()
........expandmetabolic syndrome ()
........expandmiliaria ()
........expandmultiple chemical sensitivity ()
........expandmyalgic encephalomeyelitis/chronic fatigue syndrome ()
........expandnephrotic syndrome ()
........expandobstructive sleep apnea syndrome ()
........expandpalindromic rheumatism ()
........expandPatau syndrome ()
........expandpersian gulf syndrome ()
........expandPotter syndrome ()
........expandReye syndrome ()
........expandsick sinus syndrome ()
........expandsubclavian steal syndrome ()
........expandsubstance withdrawal syndrome ()
........expandsuperior mesenteric artery syndrome ()
........expandsyndromic intellectual disability ()
........expandtarsal tunnel syndrome ()
........expandtethered spinal cord syndrome ()
........expandthoracic outlet syndrome ()
........expandTietze syndrome ()
........expandtoxic shock syndrome ()
........expandvertebral artery insufficiency ()
........expandWaterhouse-Friderichsen syndrome ()
........expandWissler syndrome ()



 Sister Nodes: 
..expandacute disease ()
..expandacute macular neuroretinopathy ()
..expandbiological anomaly without phenotypic characterization ()
..expandcell proliferation disorder ()
..expandcongenital abnormality ()
..expandconnective tissue disease ()
..expanddegenerative disorder ()
..expanddisease by anatomical system ()
..expanddisease by subcellular system affected ()
..expanddisorder by anatomical region ()
..expanddisorder involving pain ()
..expanddisorder of development or morphogenesis ()
..expandHinman syndrome ()
..expandiatrogenic disease ()
..expandinfectious disease ()
..expandinflammatory disease ()
..expandinherited genetic disease ()
..expandinjury ()
..expandnon-human animal disease ()
..expandnutritional or metabolic disease ()
..expandpersistent placoid maculopathy ()
..expandpost-infectious disorder ()
..expandpsychiatric disorder ()
..expandradiation or chemically induced disorder ()
..expandsyndromic disease ()
..expandsystemic or rheumatic disease ()
   

MONDO is developed by the Monarch Initiative. Human Disease MESH is developed by UMLS.
Further data from MedGen, OMIM,ClinVar, CTD
Term ID:2254
Name:syndromic disease
Definition:A group of signs, symptoms, and clinicopathological characteristics that may or may not have a genetic basis and collectively define an abnormal condition.
Alternative IDs:
ParentIDs:
TreeNumbers:
Synonyms:cluster, symptom; clusters, symptom; symptom cluster; symptom clusters; syndrome; syndrome associated with disease or disorder; syndrome associated with disease or disorder; syndromes; syndromic disease; syndromic disease or disorder
Slim Mappings:
Reference: MedGen:
MeSH:
OMIM:
MSeqDR LSDB:  
Genes:
Phenotypes
Disease Causing ClinVar Variants
MSeqDR Portal