Search Ontology:
Human Disease

hereditary spastic paraplegia 15

Term ID
DOID:0110768
Synonyms
  • autosomal recessive spastic paraplegia 15
  • autosomal recessive spastic paraplegia type 15
  • hereditary spastic paraparesis type 15
  • Kjellin syndrome
  • spastic paraplegia and retinal degeneration
  • spastic paraplegia-retinal degeneration syndrome
  • SPG15
Definition
A hereditary spastic paraplegia that has_material_basis_in mutation in the ZFYVE26 gene on chromosome 14q24.1. https://www.ncbi.nlm.nih.gov/pubmed/18394578
References
Ontology
Human Disease   ( DOID:0110768 )
Relationships
is a type of
Other Pages
Genes Involved
Zebrafish Models