Human genes for hereditary spastic paraplegia 5A
Hereditary spastic paraplegia 5A [DOID:0110810]
A hereditary spastic paraplegia that is characterized by progressive muscle weakness and paraplegia and has_material_basis_in mutation in the CYP7B1 gene on chromosome 8q12.
Synonyms: hereditary spastic paraplegia 5A, DOID:0110810, familial spastic paraplegia 5A, autosomal recessive spastic paraplegia 5A, autosomal recessive spastic paraplegia type 5A ...