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hereditary spastic paraplegia 12

Go to external page http://purl.obolibrary.org/obo/DOID_0110765

A hereditary spastic paraplegia that has_material_basis_in mutation in the RTN2 gene on chromosome 19q13. [ http://purl.obolibrary.org/obo/ECO_0007645 ]

Term info

Label

hereditary spastic paraplegia 12

Synonyms
  • SPG12
  • autosomal dominant spastic paraplegia 12
  • autosomal dominant spastic paraplegia type 12
database cross reference
has obo namespace

disease_ontology

id

DOID:0110765