Wilson disease (Q17588): Difference between revisions

Latest revision as of 21:02, 31 December 2023

multisystem disease due to abnormal accumulation of copper

Cerebral pseudosclerosis (disorder)
Westphal pseudosclerosis
Westphal-Strumpell syndrome (disorder)
hepatolenticular degeneration
Wilson's disease
Cerebral pseudosclerosis
Westphal-Strumpell syndrome
WD
Wnd
Wilson Disease

Language	Label	Description	Also known as
English	Wilson disease	multisystem disease due to abnormal accumulation of copper	Cerebral pseudosclerosis (disorder) Westphal pseudosclerosis Westphal-Strumpell syndrome (disorder) hepatolenticular degeneration Wilson's disease Cerebral pseudosclerosis Westphal-Strumpell syndrome WD Wnd Wilson Disease

Statements

instance of

designated intractable/rare diseases

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metal metabolism disorder

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copper metabolism disease

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organic brain syndrome

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rare hereditary metabolic disease with peripheral neuropathy

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metabolic disease with cataract

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metabolic disease with corneal opacity

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supranuclear oculomotor palsy

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tremor

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rare genetic tremor disorder

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rare metabolic liver disease

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metal transport or utilization disorder with epilepsy

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rare genetic epilepsy

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neurometabolic disease

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rare disorder with dystonia and other neurologic or systemic manifestation

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nephropathy secondary to a storage or other metabolic disease

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face of the giant panda sign

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exact match

http://purl.obolibrary.org/obo/DOID_893

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http://identifiers.org/doid/DOID:893

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http://www.orpha.net/ORDO/Orphanet_905

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@@ Property / subclass of @@
+metabolic disease with corneal opacity
@@ Property / subclass of: metabolic disease with corneal opacity / rank @@
+Normal rank
@@ Property / subclass of @@
+supranuclear oculomotor palsy
@@ Property / subclass of: supranuclear oculomotor palsy / rank @@
+Normal rank
@@ Property / subclass of @@
+tremor
@@ Property / subclass of: tremor / rank @@
+Normal rank
@@ Property / subclass of @@
+rare genetic tremor disorder
@@ Property / subclass of: rare genetic tremor disorder / rank @@
+Normal rank
@@ Property / subclass of @@
+rare metabolic liver disease
@@ Property / subclass of: rare metabolic liver disease / rank @@
+Normal rank
@@ Property / subclass of @@
+metal transport or utilization disorder with epilepsy
+Normal rank
@@ Property / subclass of @@
+rare genetic epilepsy
@@ Property / subclass of: rare genetic epilepsy / rank @@
+Normal rank
@@ Property / subclass of @@
+neurometabolic disease
@@ Property / subclass of: neurometabolic disease / rank @@
+Normal rank
@@ Property / subclass of @@
+rare disorder with dystonia and other neurologic or systemic manifestation
+Normal rank
@@ Property / subclass of @@
+nephropathy secondary to a storage or other metabolic disease
+Normal rank
@@ Property / subclass of @@
+disease
@@ Property / subclass of: disease / rank @@
+Normal rank
@@ Property / has cause @@
+genetics
@@ Property / has cause: genetics / rank @@
+Normal rank
@@ Property / health specialty @@
+endocrinology
@@ Property / health specialty: endocrinology / rank @@
+Normal rank
@@ Property / symptoms and signs @@
+edema
@@ Property / symptoms and signs: edema / rank @@
+Normal rank
@@ Property / symptoms and signs @@
+jaundice
@@ Property / symptoms and signs: jaundice / rank @@
+Normal rank
@@ Property / symptoms and signs @@
+personality changes
@@ Property / symptoms and signs: personality changes / rank @@
+Normal rank
@@ Property / symptoms and signs @@
+blue nails
@@ Property / symptoms and signs: blue nails / rank @@
+Normal rank
@@ Property / symptoms and signs @@
+face of the giant panda sign
@@ Property / symptoms and signs: face of the giant panda sign / rank @@
+Normal rank
@@ Property / exact match @@
+http://purl.obolibrary.org/obo/DOID_893
@@ Property / exact match: http://purl.obolibrary.org/obo/DOID_893 / rank @@
+Normal rank
@@ Property / exact match @@
+http://identifiers.org/doid/DOID:893
@@ Property / exact match: http://identifiers.org/doid/DOID:893 / rank @@
+Normal rank
@@ Property / exact match @@
+http://www.orpha.net/ORDO/Orphanet_905
@@ Property / exact match: http://www.orpha.net/ORDO/Orphanet_905 / rank @@
+Normal rank

Wilson disease (Q17588): Difference between revisions

Latest revision as of 21:02, 31 December 2023

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Wilson disease (Q17588): Difference between revisions

Latest revision as of 21:02, 31 December 2023

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⧼wikibase-sitelinks-mywikigroup⧽(0 entries)

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