Autosomal dominant spastic paraplegia type 19 (Q100872): Difference between revisions
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Revision as of 17:39, 16 August 2026
Autosomal dominant spastic paraplegia associated with SPG19 gene that presents with slowly progressive spastic paraplegia presenting in adulthood with spastic gait, lower limb hyperreflexia, extensor plantar responses, bladder dysfunction, and mild sensory and motor peripheral neuropathy.
| Language | Label | Description | Also known as |
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| default for all languages | ID_1020508875 |
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| English | Autosomal dominant spastic paraplegia type 19 |
Autosomal dominant spastic paraplegia associated with SPG19 gene that presents with slowly progressive spastic paraplegia presenting in adulthood with spastic gait, lower limb hyperreflexia, extensor plantar responses, bladder dysfunction, and mild sensory and motor peripheral neuropathy. |
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CID11:ID_1020508875
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