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(Q21681)
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Revision as of 21:05, 2 April 2024 by
Fire
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Created claim:
exact match
(P409)
: http://www.orpha.net/ORDO/Orphanet_1429)
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Statements
instance of
rare disease
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class of disease
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symptom or sign
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subclass of
movement disorders
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Huntington's disease-like syndrome
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clinical sign
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involuntary movement
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disease
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health specialty
neurology
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exact match
http://purl.obolibrary.org/obo/DOID_12859
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http://identifiers.org/doid/DOID:12859
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http://www.orpha.net/ORDO/Orphanet_1429
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Sitelinks
⧼wikibase-sitelinks-mywikigroup⧽
(0 entries)
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