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Human Disease

hereditary spastic paraplegia 26

Term ID
DOID:0110777
Synonyms
  • autosomal recessive spastic paraplegia 26
  • autosomal recessive spastic paraplegia type 26
  • GM2 synthase deficiency
  • SPG26
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
References
Ontology
Human Disease   ( DOID:0110777 )
Relationships
is a type of
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Genes Involved
Zebrafish Models