hereditary spastic paraplegia 53

Term ID

DOID:0110805

Synonyms

autosomal recessive spastic paraplegia 53
autosomal recessive spastic paraplegia type 53
SPG53

Definition

A hereditary spastic paraplegia that has_material_basis_in mutation in the VPS37A gene on chromosome 8p22. https://www.ncbi.nlm.nih.gov/pubmed/22717650

References

ICD10CM:G11.4
OMIM:614898
ORDO:319199

Ontology

Human Disease ( DOID:0110805 )

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

Citations