Item:Q21670: Difference between revisions

Created claim: exact match (P409): http://www.orpha.net/ORDO/Orphanet_399
 
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Property / instance of
 
Property / instance of: rare disease / rank
 
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Property / instance of
 
Property / instance of: class of disease / rank
 
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Property / instance of
 
Property / instance of: symptom or sign / rank
 
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Property / subclass of
 
Property / subclass of: neurodegeneration / rank
 
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Property / subclass of
 
Property / subclass of: Huntington disease and related disorders / rank
 
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Property / subclass of
 
Property / subclass of: eye degenerative disease / rank
 
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Property / subclass of
 
Property / subclass of: genetic neurodegenerative disease with dementia / rank
 
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Property / subclass of
 
Property / subclass of: trinucleotide repeat disorder / rank
 
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Property / subclass of
 
Property / subclass of: disease / rank
 
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Property / has cause
 
Property / has cause: trinucleotide repeat expansion / rank
 
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Property / has cause: trinucleotide repeat expansion / qualifier
 
Property / health specialty
 
Property / health specialty: neurology / rank
 
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Property / symptoms and signs
 
Property / symptoms and signs: personality changes / rank
 
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Property / symptoms and signs
 
Property / symptoms and signs: choreatic disease / rank
 
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Property / symptoms and signs
 
Property / symptoms and signs: weight loss / rank
 
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Property / symptoms and signs
 
Property / symptoms and signs: dementia / rank
 
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Property / described at URL
 
Property / described at URL: https://lirh.it/it/come-si-manifesta-la-malattia-di-huntington / rank
 
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Property / exact match
 
Property / exact match: http://purl.obolibrary.org/obo/DOID_12858 / rank
 
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Property / exact match
 
Property / exact match: http://identifiers.org/doid/DOID:12858 / rank
 
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Property / exact match
 
Property / exact match: http://www.orpha.net/ORDO/Orphanet_248111 / rank
 
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Property / exact match
 
Property / exact match: http://www.orpha.net/ORDO/Orphanet_399 / rank
 
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