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Metadata
ID DOID:0110805
Name hereditary spastic paraplegia 53
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
Xrefs

ICD10CM:G11.4

OMIM:614898

ORDO:319199

Synonyms

autosomal recessive spastic paraplegia 53 [EXACT]

autosomal recessive spastic paraplegia type 53 [EXACT]

SPG53 [EXACT]

Parent Relationships

is_a hereditary spastic paraplegia

is_a autosomal recessive disease

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