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Human Disease

hereditary spastic paraplegia 10

Term ID
DOID:0110763
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 )
Relationships
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Genes Involved
Zebrafish Models