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visceral heterotaxy
Disease Summary
Associated Targets (36)
Tbio
33
Tdark
2
Tchem
1
Mondo Description A rare, genetic disorder in which symptoms are generally secondary to the abnormal location of the organs within the thoracic, abdominal, or peritoneal cavities. Anatomic and functional problems can include cardiac defects, intestinal malrotation leading to volvulus, biliary atresia, and various defects of the central nervous system, urinary tract, and skeleton.
Disease Ontology Description A physical disorder characterized by the abnormal distribution of the major visceral organs within the chest and abdomen.
Counts of Target Development Levels for diseases known to be associated with this disease. If the disease has a valid DOID, targets known to be associated with all child diseases are aggregated. Click "Explore Associated Targets" to view more facets and details for the target list.
Description from Mondo Disease Ontology.
Description from Disease Ontology
DataSources which have contributed target associations to this disease, and the identifiers by which the disease is referenced.
DOID:0050545
EFO:0009081
NCIT:C117273
OMIMPS:306955
Orphanet:450
UMLS:C3178805
MONDO:0018677
High level summary of knowledge for a disease, including descriptions and datasource references.