| Metadata | |
|---|---|
| ID | DOID:0110771 |
| Name | hereditary spastic paraplegia 18 |
| Definition | A hereditary spastic paraplegia that has_material_basis_in mutation in the ERLIN2 gene on chromosome 8p11. https://www.ncbi.nlm.nih.gov/pubmed/21330303 |
| Xrefs | |
| Subsets |
DO_rare_slim |
| Synonyms |
autosomal recessive spastic paraplegia 18 [EXACT] autosomal recessive spastic paraplegia type 18 [EXACT] IDMDC [EXACT] intellectual disability, motor dysfunction and joint contractures [EXACT] SPG18 [EXACT] |
| Parent Relationships |