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 ) |