Term Name: | hereditary spastic paraplegia 29 |
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Synonyms: | autosomal dominant spastic paraplegia 29, SPG29 |
Definition: | A hereditary spastic paraplegia that has_material_basis_in variation in the chromosome region 1p31.1-p21.1. |
Ontology: | Human Disease [DOID:0110780] ( DOID:0110780 ) |