OBO ID: DOID:0110765
Term Name: hereditary spastic paraplegia 12 Search Ontology:
Synonyms:
  • autosomal dominant spastic paraplegia 12
  • autosomal dominant spastic paraplegia type 12
  • SPG12
Definition: A hereditary spastic paraplegia that has_material_basis_in mutation in the RTN2 gene on chromosome 19q13. https://www.ncbi.nlm.nih.gov/pubmed/22232211
References:
Ontology: Human Disease   (DOID:0110765)
OTHER hereditary spastic paraplegia 12 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
RTN2 Spastic paraplegia 12, autosomal dominant 604805
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None