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| Term | hereditary spastic paraplegia 85 | ID (Ontology) | DOID:0112345 (Human Disease) |
| Definition | A hereditary spastic paraplegia characterized by onset of motor symptoms (e.g. spasticity and hyperreflexia of the lower limbs) in the first few years of life that has_material_basis_in homozygous or compound heterozygous mutation in the RNF170 gene on chromosome 8p11.21. | ||
| Also Known As | "spastic paraplegia 85 autosomal recessive" ; "SPG85" | ||
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autosomal genetic disease |__autosomal recessive disease____ paraplegia | |__hereditary spastic paraplegia__| hereditary spastic paraplegia 85 |
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autosomal recessive disease hereditary spastic paraplegia |
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| MIM:619686 | |||