hereditary spastic paraplegia 35 (Q32142909)
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A hereditary spastic paraplegia that has material basis in mutation in the FA2H gene on chromosome 16q23.1.
- FAHN
- leukodystrophy, dysmyelinating and spastic paraparesis with or without dystonia
- autosomal recessive spastic paraplegia type 35
- autosomal recessive spastic paraplegia 35
- fatty acid hydroxylase-associated neurodegeneration
- SPG35
- SPASTIC PARAPLEGIA 35, AUTOSOMAL RECESSIVE
- hereditary spastic paraplegia type 35
- SPASTIC PARAPLEGIA 35, AUTOSOMAL RECESSIVE; SPG35
- Leukodystrophy, Dysmyelinating, and Spastic Paraparesis With or Without Dystonia
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | hereditary spastic paraplegia 35 |
A hereditary spastic paraplegia that has material basis in mutation in the FA2H gene on chromosome 16q23.1. |
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C188989
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