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(Q17588)
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Revision as of 15:48, 31 December 2023 by
Fire
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Created claim:
subclass of
(P1)
:
rare genetic epilepsy
(Q17615)
)
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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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Sitelinks
⧼wikibase-sitelinks-mywikigroup⧽
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