Human genes for hereditary spastic paraplegia 35
Hereditary spastic paraplegia 35 [DOID:0110786]
A hereditary spastic paraplegia that has_material_basis_in mutation in the FA2H gene on chromosome 16q23.1.
Synonyms: hereditary spastic paraplegia 35, DOID:0110786, familial spastic paraplegia 35, autosomal recessive spastic paraplegia 35, autosomal recessive spastic paraplegia type 35 ...