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16110005 Ophthalmoplegia
16110005 Ophthalmoplegia
Summary
- Status: Active
- Version: 20220731
- Last Changed: 2022-07-31
- definitionStatusId: 900000000000074008 | Primitive
- module: 999991001000101 | IPS terminology module
Text Definitions
- Ophthalmoplegia refers to a medical condition characterized by weakness or paralysis of the muscles that control eye movement, resulting in limited or complete loss of eye mobility.
Descriptions
Suggest Synonym- Ophthalmoplegia [ 900000000000013009 Synonym en,
en_GB
]
- Ophthalmoplegia (disorder) [ 900000000000003001 Fully specified name en_GB,
en
]
Parent Concepts
- 127346000 Neurologic disorder of eye movements
- 29426003 Paralytic syndrome
Child Concepts
Suggest Child Concept- 28978003 Progressive supranuclear ophthalmoplegia
Defining Attributes
Refsets
NoneMapsets
- 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=16110005#content
- SNOMED IPS Browser - https://ips-browser.ihtsdotools.org/?perspective=full&conceptId1=16110005&edition=MAIN/2022-07-31
JSON Document
{ "conceptId": "16110005", "fsn": { "term": "Ophthalmoplegia (disorder)", "lang": "en" }, "active": true, "effectiveTime": "20220731", "definitionStatus": "PRIMITIVE", "descriptions": [ { "active": true, "term": "Ophthalmoplegia (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": "127346000", "active": true, "definitionStatus": "PRIMITIVE", "fsn": { "term": "Neurologic disorder of eye movements (disorder)" } }, "groupId": 0 }, { "active": true, "typeId": "116680003", "type": { "conceptId": "116680003", "fsn": { "term": "Is a (attribute)" } }, "target": { "conceptId": "29426003", "active": true, "definitionStatus": "PRIMITIVE", "fsn": { "term": "Paralytic syndrome (disorder)" } }, "groupId": 0 }, { "active": true, "typeId": "363698007", "type": { "conceptId": "363698007", "fsn": { "term": "Finding site (attribute)" } }, "target": { "conceptId": "25087005", "active": true, "definitionStatus": "PRIMITIVE", "fsn": { "term": "Structure of nervous system (body structure)" } }, "groupId": 1 }, { "active": true, "typeId": "363698007", "type": { "conceptId": "363698007", "fsn": { "term": "Finding site (attribute)" } }, "target": { "conceptId": "49549006", "active": true, "definitionStatus": "PRIMITIVE", "fsn": { "term": "Structure of visual system (body structure)" } }, "groupId": 2 } ] }
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