loading...| Preferred Name |
Heterotaxy Syndrome |
|
| Synonyms |
Heterotaxia Syndrome Heterotaxy Syndrome |
|
| Definitions |
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. |
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| ID |
http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C117273 |
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| code |
C117273 |
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| Concept_In_Subset | ||
| 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 Heterotaxy Syndrome |
|
| label |
Heterotaxy Syndrome |
|
| Preferred_Name |
Heterotaxy Syndrome |
|
| prefixIRI |
Thesaurus:C117273 |
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| Semantic_Type |
Disease or Syndrome |
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| UMLS_CUI |
C3178805 |
|
| subClassOf |