OBO ID: DOID:0110763
Term Name: hereditary spastic paraplegia 10 Search Ontology:
Synonyms:
  • autosomal dominant spastic paraplegia 10
  • autosomal dominant spastic paraplegia type 10
  • SPG10
Definition: A hereditary spastic paraplegia that has_material_basis_in mutation in the KIF5A gene on chromosome 12q13. https://www.ncbi.nlm.nih.gov/pubmed/12355402
References:
Ontology: Human Disease   (DOID:0110763)
OTHER hereditary spastic paraplegia 10 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
KIF5A Spastic paraplegia 10, autosomal dominant 604187
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None