OBO ID: DOID:0110798
Term Name: hereditary spastic paraplegia 46 Search Ontology:
Synonyms:
  • autosomal recessive spastic paraplegia 46
  • autosomal recessive spastic paraplegia type 46
  • SPG46
Definition: A hereditary spastic paraplegia that has_material_basis_in mutation in the GBA2 gene on chromosome 9p. https://www.ncbi.nlm.nih.gov/pubmed/23332916
References:
Ontology: Human Disease   (DOID:0110798)
OTHER hereditary spastic paraplegia 46 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
GBA2 Spastic paraplegia 46, autosomal recessive 614409
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None