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:
expanddisease or disorder (MONDO:0000001)
..Starting node
..expandacute disease ()

       Child Nodes:
........expandacute adenoiditis ()
........expandacute bronchiolitis ()
........expandacute cervicitis ()
........expandacute cholangitis ()
........expandacute closed-angle glaucoma ()
........expandacute conjunctivitis ()
........expandacute cor pulmonale ()
........expandacute cystitis (disease) ()
........expandacute dacryoadenitis ()
........expandacute dacryocystitis ()
........expandacute diarrhea ()
........expandacute diffuse glomerulonephritis ()
........expandacute endometritis ()
........expandacute endophthalmitis ()
........expandacute ethmoiditis ()
........expandacute eustachian salpingitis ()
........expandacute frontal sinusitis ()
........expandacute gonococcal epididymo-orchitis ()
........expandacute gonococcal prostatitis ()
........expandacute graft versus host disease ()
........expandacute hypotension ()
........expandacute idiopathic urticaria ()
........expandacute kidney failure ()
........expandacute laryngitis ()
........expandacute lymphoblastic leukemia (disease) ()
........expandacute maxillary sinusitis ()
........expandacute myeloid leukemia ()
........expandacute myocardial infarction ()
........expandacute myocarditis ()
........expandacute neonatal citrullinemia type I ()
........expandacute otitis externa ()
........expandacute pancreatitis ()
........expandacute papillary necrosis ()
........expandacute pericementitis ()
........expandacute pharyngitis ()
........expandacute proliferative glomerulonephritis ()
........expandacute pyelonephritis ()
........expandacute respiratory failure ()
........expandacute retrobulbar neuritis ()
........expandacute salpingitis ()
........expandacute sphenoidal sinusitis ()
........expandacute thyroiditis ()
........expandacute transudative otitis media ()
........expanddysentery ()
........expandencephalitis ()
........expandencephalopathy, acute, infection-induced ()
........expandpoliomyelitis ()
........expandpurulent acute otitis media ()
........expandseminal vesicle acute gonorrhea ()
........expandsudden hearing loss disorder ()



 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:20683
Name:acute disease
Definition:Disease having a short and relatively severe course.
Alternative IDs:
ParentIDs:
TreeNumbers:
Synonyms:acute Disease; acute disease; acute disease; acute Diseases; Disease, Acute; Diseases, Acute
Slim Mappings:
Reference: MedGen:
MeSH:
OMIM:
MSeqDR LSDB:  
Genes:
Phenotypes
Disease Causing ClinVar Variants
MSeqDR Portal