hereditary spastic paraplegia 10

Term ID

DOID:0110763

Synonyms

• autosomal dominant spastic paraplegia 10
• autosomal dominant spastic paraplegia type 10
• SPG10

Definition

A hereditary spastic paraplegia that has_material_basis_in mutation in the KIF5A gene on chromosome 12q13. https://www.ncbi.nlm.nih.gov/pubmed/12355402

References

• GARD:9590
• ICD10CM:G11.4
• OMIM:604187
• ORDO:100991

Ontology

Human Disease   ( DOID:0110763 )