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Diseases
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Nervous system disorder
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Hereditary neurological disease
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Hereditary neuromuscular disease
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Hereditary spastic paraplegia
Spastic paraplegia 79A, autosomal dominant, with ataxia
rare
Identifiers
MONDO:0859363
OMIM:620221
Causal genes
UCHL1
Part of
Hereditary spastic paraplegia
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