Term Name: hereditary spastic paraplegia 19
Synonyms: autosomal dominant spastic paraplegia 19, autosomal dominant spastic paraplegia type 19, SPG19
Definition: A hereditary spastic paraplegia that has_material_basis_in variation in the chromosome region 9q.
Ontology: Human Disease [DOID:0110772]   ( DOID:0110772 )

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