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Collaborative Research
Diseases
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Nervous system disorder
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Hereditary neurological disease
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Inherited neurodegenerative disorder
Neurodegeneration, childhood-onset, with cerebellar atrophy
rare
Identifiers
MONDO:0032650
OMIM:618276
Causal genes
AGTPBP1
Part of
Inherited neurodegenerative disorder
Also known as
CONDCA
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