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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disease or disorder (MONDO:0000001)
..Starting node
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disease by anatomical system ()

       Child Nodes:
........expandcardiovascular disease ()
........expanddigestive system disease ()
........expanddisease of genitourinary system ()
........expandendocrine system disease ()
........expandhematologic disease ()
........expandimmune system disease ()
........expandintegumentary system disease ()
........expandmediastinal disease ()
........expandmusculoskeletal system disease ()
........expandnervous system disorder ()
........expandrespiratory system disease ()
........expandsensory system disease ()
........expandurinary system disease ()



 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:21199
Name:disease by anatomical system
Definition:A disease that disrupts the functioning of an organ system.
Alternative IDs:
ParentIDs:
TreeNumbers:
Synonyms:anatomical system disease; disease of anatomical entity; disease of anatomical system; disorder of anatomical system
Slim Mappings:
Reference: MedGen:
MeSH:
OMIM:
MSeqDR LSDB:  
Genes:
Phenotypes
Disease Causing ClinVar Variants
MSeqDR Portal