| Metadata | |
|---|---|
| ID | DOID:0110789 |
| Name | hereditary spastic paraplegia 38 |
| Definition | A hereditary spastic paraplegia that has_material_basis_in variation in the chromosome region 4p16-p15. https://www.ncbi.nlm.nih.gov/pubmed/18401025 |
| Xrefs | |
| Subsets |
DO_rare_slim |
| Synonyms |
autosomal dominant spastic paraplegia 38 [EXACT] autosomal dominant spastic paraplegia type 38 [EXACT] SPG38 [EXACT] |
| Parent Relationships |