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Kidney Tissue Atlas Ontology
Last uploaded:
March 16, 2024
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Id | http://purl.obolibrary.org/obo/MONDO_0018677
http://purl.obolibrary.org/obo/MONDO_0018677
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Preferred Name | visceral heterotaxy |
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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Synonyms |
situs ambiguus
heterotaxia
heterotaxy, visceral
heterotaxia syndrome
lateralization defect
heterotaxy syndrome
visceral heterotaxy
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Type | http://www.w3.org/2002/07/owl#Class |
All Properties
label |
visceral heterotaxy
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prefLabel |
visceral heterotaxy
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exactMatch | |
database_cross_reference |
UMLS:C3178805
NCIT:C117273
MedDRA:10067265
DOID:0050545
ICD10:Q89.3
Orphanet:450
EFO:0009081
OMIMPS:306955
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notation |
MONDO:0018677
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in_subset | |
has related synonym |
situs ambiguus
heterotaxia
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id |
MONDO:0018677
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should_conform_to | |
textual 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.
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subClassOf | |
imported from | |
type | |
has exact synonym |
heterotaxy, visceral
heterotaxia syndrome
lateralization defect
heterotaxy syndrome
visceral heterotaxy
|
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