Human genes for hereditary spastic paraplegia 9A
Hereditary spastic paraplegia 9A [DOID:0110824]
A hereditary spastic paraplegia that has_material_basis_in autosomal dominant heterozygous mutation in the ALDH18A1 gene on chromosome 10q24.
Synonyms: hereditary spastic paraplegia 9A, DOID:0110824, familial spastic paraplegia 9A, AD-SPG9A, autosomal dominant complex spastic paraplegia type 9A ...