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
MIM:604187
ORDO:100991

Ontology

Human Disease ( DOID:0110763 )

Relationships

is a type of: autosomal dominant disease hereditary spastic paraplegia

autosomal dominant disease hereditary spastic paraplegia Show first 5 Terms

Other Pages

Alliance (1)

Genes Involved

Zebrafish Models