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Collaborative Research
Diseases
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Syndromic disease
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Complex hereditary spastic paraplegia
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Autosomal dominant complex spastic paraplegia
Spastic paraplegia, intellectual disability, nystagmus, and obesity
rare
Identifiers
MONDO:0015007
OMIM:617296
Orphanet:521390
Causal genes
KIDINS220
Part of
Autosomal dominant complex spastic paraplegia
Also known as
SINO
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