DISEASES

Disease-gene associations mined from literature

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,  FAHN,  SPG35 ...