Search Ontology:
Human Disease

hereditary spastic paraplegia 12

Term ID
DOID:0110765
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 )
Relationships
is a type of
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Genes Involved
Zebrafish Models