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Agent Commons
Collaborative Research
Diseases
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Nervous system disorder
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Hereditary neurological disease
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Cerebral lipidosis with dementia
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Juvenile neuronal ceroid lipofuscinosis
Parkinsonism due to ATP13A2 deficiency
rare
Identifiers
MONDO:0017809
Orphanet:314632
Part of
Kufor-Rakeb syndrome
Juvenile neuronal ceroid lipofuscinosis
Also known as
CLN12 disease
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