DISEASES

Disease-gene associations mined from literature

Human genes for hereditary spastic paraplegia 32

Hereditary spastic paraplegia 32 [DOID:0110783]

A hereditary spastic paraplegia that has_material_basis_in variation in the chromosome region 14q12-q21.

Synonyms:  hereditary spastic paraplegia 32,  DOID:0110783,  familial spastic paraplegia 32,  SPG32,  autosomal recessive spastic paraplegia 32 ...