OBO ID: DOID:0110777
Term Name: hereditary spastic paraplegia 26 Search Ontology:
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)
OTHER hereditary spastic paraplegia 26 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
B4GALNT1 Spastic paraplegia 26, autosomal recessive 609195
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None