| Metadata | |
|---|---|
| ID | DOID:0110825 |
| Name | hereditary spastic paraplegia 9B |
| Definition | A hereditary spastic paraplegia that has_material_basis_in autosomal recessive homozygous or compound heterozygous mutation in the ALDH18A1 gene on chromosome 10q24. https://www.ncbi.nlm.nih.gov/pubmed/26026163 |
| Xrefs | |
| Subsets |
DO_rare_slim |
| Synonyms |
autosomal recessive complex spastic paraplegia type 9B [EXACT] autosomal recessive spastic paraplegia 9B [EXACT] SPG9B [EXACT] |
| Parent Relationships |