dystonia (Q17622): Difference between revisions
		
		
		
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|  Created claim:  subclass of (P1): rare genetic dystonia (Q17620) |  Created claim:  exact match (P409): http://www.orpha.net/ORDO/Orphanet_68363 | ||
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| Property / health specialty: neurology / rank | |||
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| Property / exact match: http://purl.obolibrary.org/obo/DOID_543 / rank | |||
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| Property / exact match: http://identifiers.org/doid/DOID:543 / rank | |||
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| Property / exact match: http://purl.obolibrary.org/obo/HP_0001332 / rank | |||
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| Property / exact match: http://www.orpha.net/ORDO/Orphanet_156159 / rank | |||
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| Property / exact match | |||
| Property / exact match: http://www.orpha.net/ORDO/Orphanet_68363 / rank | |||
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Latest revision as of 15:55, 31 December 2023
human disease
- dystonic disease
- Pure dystonia
- nonsyndromic dystonia (disease)
- rare dystonia
- rare dystonia (disease)
- Rare dystonic disorder
| Language | Label | Description | Also known as | 
|---|---|---|---|
| English | dystonia | human disease | 
 |