| Term Name: | autosomal recessive sensory neuropathy with spastic paraplegia |
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| Synonyms: | |
| Definition: | A hereditary sensory and autonomic neuropathy that has_material_basis_in homozygous mutation in the CCT5 gene on chromosome 5p15.2. |
| Ontology: | Human Disease [DOID:0061188] ( DOID:0061188 ) |