Term Name: hereditary spastic paraplegia 75
Synonyms: autosomal recessive spastic paraplegia 75, autosomal recessive spastic paraplegia type 75, SPG75
Definition: A hereditary spastic paraplegia that has_material_basis_in mutation in the MAG gene on chromosome 19q13.
Ontology: Human Disease [DOID:0110820]   ( DOID:0110820 )

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