OBO ID: DOID:0110768
Term Name: hereditary spastic paraplegia 15 Search Ontology:
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)
OTHER hereditary spastic paraplegia 15 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
ZFYVE26 Spastic paraplegia 15, autosomal recessive 270700
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None