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rare genetic epilepsy
?
TBD
form of epilepsy that is both rare and inborn
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Subclasses
5
Wilson's disease
Genetic multisystem copper-transport disease
Menkes disease
X-linked recessive copper-transport disorder
Fabry disease
Rare human genetic lysosomal storage disorder
Metachromatic leukodystrophy
Medical condition
2-Methylbutyryl-CoA dehydrogenase deficiency
Medical condition
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Instance of
class of disease
Subclass of
Epilepsy
Wikidata