WormBase Tree Display for DO_term: DOID:0110777
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| DOID:0110777 | Name | hereditary spastic paraplegia 26 | |||
|---|---|---|---|---|---|
| Status | Valid | ||||
| Definition | A hereditary spastic paraplegia that has_material_basis_in mutation in the B4GALNT1 gene on chromosome 12q13. | ||||
| Synonym | Exact | GM2 synthase deficiency | |||
| SPG26 | |||||
| autosomal recessive spastic paraplegia 26 | |||||
| autosomal recessive spastic paraplegia type 26 | |||||
| Parent | Is_a | DOID:2476 | |||
| DOID:0050737 | |||||
| DB_info | Database | OMIM | disease | 609195 |
