hereditary spastic paraplegia 13

Term ID

DOID:0110766

Synonyms

• autosomal dominant spastic paraplegia 13
• SPG13

Definition

A hereditary spastic paraplegia that is characterized by a pure form of the disease with late onset and has_material_basis_in mutation in the HSPD1 gene on chromosome 2q33. https://www.ncbi.nlm.nih.gov/pubmed/11898127

References

• GARD:9616
• ICD10CM:G11.4
• OMIM:605280
• ORDO:100994

Ontology

Human Disease   ( DOID:0110766 )