/
1963002 Paroxysmal nocturnal haemoglobinuria
1963002 Paroxysmal nocturnal haemoglobinuria
Summary
- Status: Active
- Version: 20220731
- Last Changed: 2022-07-31
- definitionStatusId: 900000000000074008 | Primitive
- module: 999991001000101 | IPS terminology module
Text Definitions
NoneDescriptions
Suggest Synonym- Paroxysmal nocturnal hemoglobinuria [ 900000000000013009 Synonym en
]
- Marchiafava-Micheli syndrome [ 900000000000013009 Synonym en_GB,
en
]
- PNH [ 900000000000013009 Synonym en_GB,
en
]
- Paroxysmal nocturnal haemoglobinuria [ 900000000000013009 Synonym en_GB
]
- Paroxysmal nocturnal hemoglobinuria (disorder) [ 900000000000003001 Fully specified name en_GB,
en
]
- PNH - Paroxysmal nocturnal haemoglobinuria [ 900000000000013009 Synonym en_GB
]
- PNH - Paroxysmal nocturnal hemoglobinuria [ 900000000000013009 Synonym en
]
Parent Concepts
- 323666000 Anemia due to intrinsic red cell abnormality
Child Concepts
Suggest Child ConceptDefining Attributes
NoneRefsets
- 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=1963002#content
- SNOMED IPS Browser - https://ips-browser.ihtsdotools.org/?perspective=full&conceptId1=1963002&edition=MAIN/2022-07-31
JSON Document
{ "conceptId": "1963002", "fsn": { "term": "Paroxysmal nocturnal hemoglobinuria (disorder)", "lang": "en" }, "active": true, "effectiveTime": "20220731", "definitionStatus": "PRIMITIVE", "descriptions": [ { "active": true, "term": "Paroxysmal nocturnal hemoglobinuria (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": "323666000", "active": true, "definitionStatus": "PRIMITIVE", "fsn": { "term": "Anemia due to intrinsic red cell abnormality (disorder)" } }, "groupId": 0 } ] }
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