Term Name: hereditary spastic paraplegia 2
Synonyms: spastic paraplegia type 2, SPG2, X-linked spastic paraplegia 2
Definition: A hereditary spastic paraplegia that has_material_basis_in mutation in the PLP1 gene on chromosome Xq22.2.
Ontology: Human Disease [DOID:0110773]   ( DOID:0110773 )

Relationships
is a type of: hereditary spastic paraplegia X-linked recessive disease