Term Name: hereditary spastic paraplegia 23
Synonyms: Lison syndrome, Spastic paraparesis-vitiligo-premature graying-characteristic facies syndrome, spastic paraplegia 23, spastic paraplegia with pigmentary abnormalities, SPG23
Definition: A hereditary spastic paraplegia that has_material_basis_in variation in the chromosome region 1q24-q32.
Ontology: Human Disease [DOID:0110774]   ( DOID:0110774 )

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