Metadata | |
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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 |