Term Name: hereditary spastic paraplegia 53
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.
Ontology: Human Disease [DOID:0110805]   ( DOID:0110805 )

Relationships
is a type of: autosomal recessive disease hereditary spastic paraplegia