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:
expandarthropathy (MONDO:0006816)
Parent Node:
expandcartilage disease (MONDO:0005569)
Parent Node:
expandsyndromic disease (MONDO:0002254)
..Starting node
..expandTietze syndrome ()

       Child Nodes:



 Sister 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 ()
   

MONDO is developed by the Monarch Initiative. Human Disease MESH is developed by UMLS.
Further data from MedGen, OMIM,ClinVar, CTD
Term ID:1858
Name:Tietze syndrome
Definition:Idiopathic painful nonsuppurative swellings of one or more costal cartilages, especially of the second rib. The anterior chest pain may mimic that of coronary artery disease. (Dorland, 27th ed.)
Alternative IDs:
ParentIDs:
TreeNumbers:
Synonyms:Chondropathia tuberosa; Costalchondritis; costochondral joint syndromic disease; costochondral junction syndrome; Costochondritis; slipping rib syndrome; syndromic disease of costochondral joint; Tietze syndrome; Tietze's disease; Tietze's syndrome
Slim Mappings:
Reference: MedGen:
MeSH:
OMIM:
MSeqDR LSDB:  
Genes:
Phenotypes
Disease Causing ClinVar Variants
MSeqDR Portal