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
MIM:603563
ORDO:100989

Ontology

Human Disease ( DOID:0110823 )

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