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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
OMIM: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

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Alliance (1)

Genes Involved

Zebrafish Models

Citations