| Metadata | |
|---|---|
| ID | DOID:0110765 |
| Name | hereditary spastic paraplegia 12 |
| Definition | A hereditary spastic paraplegia that has_material_basis_in mutation in the RTN2 gene on chromosome 19q13. https://www.ncbi.nlm.nih.gov/pubmed/22232211 |
| Xrefs | |
| Subsets |
DO_rare_slim |
| Synonyms |
autosomal dominant spastic paraplegia 12 [EXACT] autosomal dominant spastic paraplegia type 12 [EXACT] SPG12 [EXACT] |
| Parent Relationships |