hereditary spastic paraplegia 11 (Q32142563)
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hereditary spastic paraplegia that has material basis in mutation in the SPG11 gene on chromosome 15q21
- spastic paraplegia-intellectual disability-thin corpus callosum syndrome
- autosomal recessive spastic paraplegia type 11
- autosomal recessive spastic paraplegia complicated with thin corpus callosum
- autosomal recessive spastic paraplegia 11
- Nakamura-Osame syndrome
- SPG11
- autosomal recessive spastic paraplegia with mental impairment and thin corpus callosum
- HSP-TCC
- Spastic Paraplegia, Autosomal Recessive, Complicated, With Thin Corpus Callosum
- hereditary spastic paraplegia type 11
- Spastic Paraplegia, Autosomal Recessive, With Mental Impairment and Thin Corpus Callosum
- SPASTIC PARAPLEGIA 11, AUTOSOMAL RECESSIVE
- SPASTIC PARAPLEGIA 11, AUTOSOMAL RECESSIVE; SPG11
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | hereditary spastic paraplegia 11 |
hereditary spastic paraplegia that has material basis in mutation in the SPG11 gene on chromosome 15q21 |
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