DISEASES

Disease-gene associations mined from literature

Human genes for hereditary spastic paraplegia 53

Hereditary spastic paraplegia 53 [DOID:0110805]

A hereditary spastic paraplegia that has_material_basis_in mutation in the VPS37A gene on chromosome 8p22.

Synonyms:  hereditary spastic paraplegia 53,  DOID:0110805,  familial spastic paraplegia 53,  SPG53,  autosomal recessive spastic paraplegia 53 ...