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

• GARD:9586
• ICD10CM:G11.4
• OMIM:604805
• ORDO:100993

Ontology

Human Disease   ( DOID:0110765 )