Term Name: hereditary spastic paraplegia 45
Synonyms: autosomal recessive spastic paraplegia 45, autosomal recessive spastic paraplegia type 45, autosomal recessive spastic paraplegia type 65, SPG45, SPG65
Definition: A hereditary spastic paraplegia that has_material_basis_in mutation in the NT5C2 gene on chromosome 10q24.
Ontology: Human Disease [DOID:0110797]   ( DOID:0110797 )

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