| Metadata | |
|---|---|
| ID | DOID:0110766 |
| Name | hereditary spastic paraplegia 13 |
| Definition | A hereditary spastic paraplegia that is characterized by a pure form of the disease with late onset and has_material_basis_in mutation in the HSPD1 gene on chromosome 2q33. https://www.ncbi.nlm.nih.gov/pubmed/11898127 |
| Xrefs | |
| Subsets |
DO_rare_slim |
| Synonyms |
autosomal dominant spastic paraplegia 13 [EXACT] SPG13 [EXACT] |
| Parent Relationships | |
| Subclass Logical Relationships |
has material basis in some autosomal dominant inheritance |