OBO ID: DOID:0110823
Term Name: hereditary spastic paraplegia 8 Search Ontology:
Synonyms:
  • autosomal dominant spastic paraplegia 8
  • autosomal dominant spastic paraplegia type 8
  • SPG8
Definition: A hereditary spastic paraplegia that has_material_basis_in mutation in the KIAA0196 gene on chromosome 8q24. https://www.ncbi.nlm.nih.gov/pubmed/17160902
References:
Ontology: Human Disease   (DOID:0110823)
OTHER hereditary spastic paraplegia 8 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
WASHC5 Spastic paraplegia 8, autosomal dominant 603563
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None