FB2025_05 , released December 11, 2025
FB2025_05 , released December 11, 2025
CV Term Report
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General Information
Term autosomal recessive sensory neuropathy with spastic paraplegia ID (Ontology) DOID:0061188 (Human Disease)
Definition A hereditary sensory neuropathy that has_material_basis_in homozygous mutation in the CCT5 gene." [url:https\://pubmed.ncbi.nlm.nih.gov/16333315/] {comment="One such family has been reported."}
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 autosomal recessive sensory neuropathy with spastic paraplegia       1
 for disease ribbon | autosomal recessive sensory neuropathy with spastic paraplegia       1
 model of | autosomal recessive sensory neuropathy with spastic paraplegia       1
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autosomal genetic disease
 |__autosomal recessive disease____
neuropathy                         |
 |__hereditary sensory neuropathy__|
                                   autosomal recessive sensory neuropathy with spastic paraplegia  1 rec.
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Is a hereditary sensory neuropathy
autosomal recessive disease
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MIM:256840