National Cancer Institute Thesaurus

Last uploaded: February 21, 2019

Preferred Name	Heterotaxy Syndrome
ID	http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C117273
code	C117273
Concept_In_Subset	http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C90259 http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C99147
Contributing_Source	NICHD
DEFINITION	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.
FULL_SYN	Heterotaxia Syndrome
Has_NICHD_Parent	http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C36287
label	Heterotaxy Syndrome
NICHD_Hierarchy_Term	Heterotaxy Syndrome
Preferred_Name	Heterotaxy Syndrome
prefixIRI	C117273
prefLabel	Heterotaxy Syndrome
Semantic_Type	Disease or Syndrome
UMLS_CUI	C3178805
subClassOf	http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C53543 http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C28193

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Delete	Mapping To	Ontology	Source
	http://purl.bioontology.org/ontology/MESH/D059446	Medical Subject Headings	LOOM