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Revision as of 21:06, 2 April 2024 by
Fire
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Created claim:
exact match
(P409)
: http://www.orpha.net/ORDO/Orphanet_248111)
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Statements
instance of
designated intractable/rare diseases
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rare disease
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class of disease
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symptom or sign
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subclass of
neurodegeneration
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Huntington disease and related disorders
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eye degenerative disease
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genetic neurodegenerative disease with dementia
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trinucleotide repeat disorder
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disease
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has cause
trinucleotide repeat expansion
of
HTT
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health specialty
neurology
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symptoms and signs
personality changes
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choreatic disease
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weight loss
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dementia
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described at URL
https://lirh.it/it/come-si-manifesta-la-malattia-di-huntington
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exact match
http://purl.obolibrary.org/obo/DOID_12858
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http://identifiers.org/doid/DOID:12858
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http://www.orpha.net/ORDO/Orphanet_248111
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Sitelinks
⧼wikibase-sitelinks-mywikigroup⧽
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