| Metadata | |
|---|---|
| ID | DOID:0110764 |
| Name | hereditary spastic paraplegia 11 |
| Definition | A hereditary spastic paraplegia that has_material_basis_in mutation in the SPG11 gene on chromosome 15q21. https://www.ncbi.nlm.nih.gov/pubmed/17322883 |
| Xrefs | |
| Subsets |
DO_rare_slim |
| Synonyms |
autosomal recessive spastic paraplegia 11 [EXACT] autosomal recessive spastic paraplegia complicated with thin corpus callosum [EXACT] autosomal recessive spastic paraplegia type 11 [EXACT] autosomal recessive spastic paraplegia with mental impairment and thin corpus callosum [EXACT] HSP-TCC [EXACT] Nakamura-Osame syndrome [EXACT] spastic paraplegia-intellectual disability-thin corpus callosum syndrome [EXACT] SPG11 [EXACT] |
| Parent Relationships |