rare disorder with dystonia and other neurologic or systemic manifestation (Q17619): 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_370106 |
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| Property / exact match | |||
| Property / exact match: http://www.orpha.net/ORDO/Orphanet_370106 / rank | |||
Normal rank | |||
Latest revision as of 15:58, 31 December 2023
human disease
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | rare disorder with dystonia and other neurologic or systemic manifestation |
human disease |