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69771008 Congenital anomaly of oesophagus
69771008 Congenital anomaly of oesophagus
Summary
- Status: Active
- Version: 20220731
- Last Changed: 2022-07-31
- definitionStatusId: 900000000000073002 | Defined
- module: 999991001000101 | IPS terminology module
Text Definitions
- A congenital anomaly of the esophagus is a birth defect in which the esophagus, the tube connecting the mouth to the stomach, is malformed or improperly developed, potentially causing difficulties in swallowing, breathing, or digestion.
Descriptions
Suggest Synonym- Congenital anomaly of esophagus [ 900000000000013009 Synonym en
]
- Congenital anomaly of oesophagus [ 900000000000013009 Synonym en_GB
]
- Congenital abnormality of esophagus [ 900000000000013009 Synonym en
]
- Congenital malformation of the esophagus [ 900000000000013009 Synonym en
]
- Congenital abnormality of oesophagus [ 900000000000013009 Synonym en_GB
]
- Congenital malformation of the oesophagus [ 900000000000013009 Synonym en_GB
]
- Congenital anomaly of esophagus (disorder) [ 900000000000003001 Fully specified name en,
en_GB
]
Parent Concepts
- 276654001 Congenital malformation
- 37657006 Disorder of oesophagus
Child Concepts
Suggest Child ConceptDefining Attributes
Refsets
- 787778008 Global Patient Set 2022
Mapsets
- 6011000124106 ICD-10-CM complex map reference set
Diagram
Browser Links
- West Coast Informatics Browser - https://ips.terminology.tools/terminology-ui/index.html#/terminology?terminology=SNOMEDCT&code=69771008#content
- SNOMED IPS Browser - https://ips-browser.ihtsdotools.org/?perspective=full&conceptId1=69771008&edition=MAIN/2022-07-31
JSON Document
{ "conceptId": "69771008", "fsn": { "term": "Congenital anomaly of esophagus (disorder)", "lang": "en" }, "active": true, "effectiveTime": "20220731", "definitionStatus": "FULLY_DEFINED", "descriptions": [ { "active": true, "term": "Congenital anomaly of esophagus (disorder)", "typeId": "900000000000003001", "acceptabilityMap": { "900000000000508004": "Preferred (foundation metadata concept)", "900000000000509007": "Preferred (foundation metadata concept)" } } ], "relationships": [ { "active": true, "typeId": "116680003", "type": { "conceptId": "116680003", "fsn": { "term": "Is a (attribute)" } }, "target": { "conceptId": "276654001", "active": true, "definitionStatus": "FULLY_DEFINED", "fsn": { "term": "Congenital malformation (disorder)" } }, "groupId": 0 }, { "active": true, "typeId": "116680003", "type": { "conceptId": "116680003", "fsn": { "term": "Is a (attribute)" } }, "target": { "conceptId": "37657006", "active": true, "definitionStatus": "FULLY_DEFINED", "fsn": { "term": "Disorder of esophagus (disorder)" } }, "groupId": 0 }, { "active": true, "typeId": "116676008", "type": { "conceptId": "116676008", "fsn": { "term": "Associated morphology (attribute)" } }, "target": { "conceptId": "49755003", "active": true, "definitionStatus": "PRIMITIVE", "fsn": { "term": "Morphologically abnormal structure (morphologic abnormality)" } }, "groupId": 1 }, { "active": true, "typeId": "246454002", "type": { "conceptId": "246454002", "fsn": { "term": "Occurrence (attribute)" } }, "target": { "conceptId": "255399007", "active": true, "definitionStatus": "PRIMITIVE", "fsn": { "term": "Congenital (qualifier value)" } }, "groupId": 1 }, { "active": true, "typeId": "363698007", "type": { "conceptId": "363698007", "fsn": { "term": "Finding site (attribute)" } }, "target": { "conceptId": "32849002", "active": true, "definitionStatus": "PRIMITIVE", "fsn": { "term": "Esophageal structure (body structure)" } }, "groupId": 1 }, { "active": true, "typeId": "370135005", "type": { "conceptId": "370135005", "fsn": { "term": "Pathological process (attribute)" } }, "target": { "conceptId": "308490002", "active": true, "definitionStatus": "PRIMITIVE", "fsn": { "term": "Pathological developmental process (qualifier value)" } }, "groupId": 1 } ] }
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