Phenotypes for disease #05927 (SPOAN (paraplegia, spastic, optic atrophy, and neuropathy (SPOAN)), OMIM:609541)

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0000267001 spastic paraplegia, optic atrophy, neuropathy SPOAN progressive spastic paraplegia in infancy, progressive motor and sensory axonal neuropathy in late childhood/early adolescence leading to severe motor disability; >15y-wheelchair bound, progressive joint contractures, spine deformities; subnormal vision secondary to apparently non-progressive congenital optic atrophy, dysarthria starting third decade of life, exacerbated acoustic startle response; no intellectual disability Familial, autosomal recessive - - - - Johan den Dunnen 00371664
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