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| Term | Charcot-Marie-Tooth disease type 5 | ID (Ontology) | DOID:0080067 (Human Disease) |
| Definition | A Charcot-Marie-Tooth disease that is characterized by pyramidal features including extensor plantar responses, mild increase in tone, and preserved or increased reflexes but no spastic gait. | ||
| Also Known As | "hereditary motor and sensory neuropathy with pyramidal features" | ||
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| DO.org | |||
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autosomal genetic disease |__autosomal dominant disease___ neuromuscular disease | |__Charcot-Marie-Tooth disease__| Charcot-Marie-Tooth disease type 5 |
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| Is a |
autosomal dominant disease Charcot-Marie-Tooth disease |
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| MIM:600361 | |||