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(Q17588)
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Revision as of 16:19, 31 December 2023 by
Fire
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Created claim:
has cause
(P74)
:
genetics
(Q12693)
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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
liver disease
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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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disease
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has cause
genetics
0 references
Sitelinks
⧼wikibase-sitelinks-mywikigroup⧽
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