| Term Name: | hereditary spastic paraplegia 18B |
|---|---|
| Synonyms: | spastic paraplegia 18B |
| Definition: | A hereditary spastic paraplegia 18 that has_material_basis_in homozygous mutation in the ERLIN2 gene on chromosome 8p11. |
| Ontology: | Human Disease [DOID:0070641] ( DOID:0070641 ) |