hereditary spastic paraplegia 8

Term ID

DOID:0110823

Synonyms

• autosomal dominant spastic paraplegia 8
• autosomal dominant spastic paraplegia type 8
• SPG8

Definition

A hereditary spastic paraplegia that has_material_basis_in mutation in the KIAA0196 gene on chromosome 8q24. https://www.ncbi.nlm.nih.gov/pubmed/17160902

References

• GARD:9591
• ICD10CM:G11.4
• OMIM:603563
• ORDO:100989

Ontology

Human Disease   ( DOID:0110823 )