/
78572006 Neurocutaneous syndrome
78572006 Neurocutaneous syndrome
Summary
- Status: Active
- Version: 20220731
- Last Changed: 2022-07-31
- definitionStatusId: 900000000000074008 | Primitive
- module: 999991001000101 | IPS terminology module
Text Definitions
NoneDescriptions
Suggest Synonym- Neuroectodermal dysplasia [ 900000000000013009 Synonym en_GB,
en
]
- Neurocutaneous syndrome [ 900000000000013009 Synonym en_GB,
en
]
- Phacomatosis [ 900000000000013009 Synonym en,
en_GB
]
- Phakomatosis [ 900000000000013009 Synonym en,
en_GB
]
- Neurocutaneous syndrome (disorder) [ 900000000000003001 Fully specified name en_GB,
en
]
- Phakomatoses [ 900000000000013009 Synonym en,
en_GB
]
Parent Concepts
- 118940003 Disorder of nervous system
- 126488004 Neoplasm of skin
- 66091009 Congenital disease
Child Concepts
Suggest Child Concept- 19133005 Neurofibromatosis syndrome
- 46659004 Von Hippel-Lindau syndrome
- 7199000 Tuberous sclerosis syndrome
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=78572006#content
- SNOMED IPS Browser - https://ips-browser.ihtsdotools.org/?perspective=full&conceptId1=78572006&edition=MAIN/2022-07-31
JSON Document
{ "conceptId": "78572006", "fsn": { "term": "Neurocutaneous syndrome (disorder)", "lang": "en" }, "active": true, "effectiveTime": "20220731", "definitionStatus": "PRIMITIVE", "descriptions": [ { "active": true, "term": "Neurocutaneous syndrome (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": "118940003", "active": true, "definitionStatus": "FULLY_DEFINED", "fsn": { "term": "Disorder of nervous system (disorder)" } }, "groupId": 0 }, { "active": true, "typeId": "116680003", "type": { "conceptId": "116680003", "fsn": { "term": "Is a (attribute)" } }, "target": { "conceptId": "126488004", "active": true, "definitionStatus": "FULLY_DEFINED", "fsn": { "term": "Neoplasm of skin (disorder)" } }, "groupId": 0 }, { "active": true, "typeId": "116680003", "type": { "conceptId": "116680003", "fsn": { "term": "Is a (attribute)" } }, "target": { "conceptId": "66091009", "active": true, "definitionStatus": "FULLY_DEFINED", "fsn": { "term": "Congenital disease (disorder)" } }, "groupId": 0 }, { "active": true, "typeId": "116676008", "type": { "conceptId": "116676008", "fsn": { "term": "Associated morphology (attribute)" } }, "target": { "conceptId": "108369006", "active": true, "definitionStatus": "PRIMITIVE", "fsn": { "term": "Neoplasm (morphologic abnormality)" } }, "groupId": 1 }, { "active": true, "typeId": "363698007", "type": { "conceptId": "363698007", "fsn": { "term": "Finding site (attribute)" } }, "target": { "conceptId": "39937001", "active": true, "definitionStatus": "PRIMITIVE", "fsn": { "term": "Skin structure (body structure)" } }, "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": 2 }, { "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": 3 } ] }
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