Search Ontology:

Human Disease

hereditary spastic paraplegia 46

Term ID

DOID:0110798

Synonyms

autosomal recessive spastic paraplegia 46
autosomal recessive spastic paraplegia type 46
SPG46

Definition

A hereditary spastic paraplegia that has_material_basis_in mutation in the GBA2 gene on chromosome 9p. https://www.ncbi.nlm.nih.gov/pubmed/23332916

References

ICD10CM:G11.4
MIM:614409
ORDO:320391

Ontology

Human Disease ( DOID:0110798 )

Relationships

is a type of: autosomal recessive disease hereditary spastic paraplegia

autosomal recessive disease hereditary spastic paraplegia Show first 5 Terms

Other Pages

Alliance (1)

Genes Involved

Zebrafish Models