| Metadata | |
|---|---|
| ID | DOID:0110777 |
| Name | hereditary spastic paraplegia 26 |
| Definition | A hereditary spastic paraplegia that has_material_basis_in mutation in the B4GALNT1 gene on chromosome 12q13. https://www.ncbi.nlm.nih.gov/pubmed/23746551 |
| Xrefs | |
| Subsets |
DO_rare_slim |
| Synonyms |
autosomal recessive spastic paraplegia 26 [EXACT] autosomal recessive spastic paraplegia type 26 [EXACT] GM2 synthase deficiency [EXACT] SPG26 [EXACT] |
| Parent Relationships |