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Disease Ontology Browser
hereditary spastic paraplegia 26 (DOID:0110777)
Alliance: disease page
Synonyms: autosomal recessive spastic paraplegia 26; autosomal recessive spastic paraplegia type 26; GM2 synthase deficiency; SPG26
Alt IDs: OMIM:609195, ICD10CM:G11.4, ORDO:101006
Definition: A hereditary spastic paraplegia that has_material_basis_in mutation in the B4GALNT1 gene on chromosome 12q13.

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB), Gene Ontology (GO)
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last database update
MGI 6.20
The Jackson Laboratory