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Metadata
ID DOID:0110798
Name hereditary spastic paraplegia 46
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
Xrefs

ICD10CM:G11.4

OMIM:614409

ORDO:320391

Synonyms

autosomal recessive spastic paraplegia 46 [EXACT]

autosomal recessive spastic paraplegia type 46 [EXACT]

SPG46 [EXACT]

Parent Relationships

is_a hereditary spastic paraplegia

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