Terminology Service for NFDI4Health
hereditary spastic paraplegia 26
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http://purl.obolibrary.org/obo/DOID_0110777
A hereditary spastic paraplegia that has_material_basis_in mutation in the B4GALNT1 gene on chromosome 12q13. [ http://purl.obolibrary.org/obo/ECO_0007645 ]
Term info
Label
hereditary spastic paraplegia 26
Synonyms
- GM2 synthase deficiency
- SPG26
- autosomal recessive spastic paraplegia 26
- autosomal recessive spastic paraplegia type 26
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disease_ontology
id
DOID:0110777