DISEASES

Disease-gene associations mined from literature

Human genes for hereditary spastic paraplegia 63

Hereditary spastic paraplegia 63 [DOID:0110814]

A hereditary spastic paraplegia that has_material_basis_in mutation in the AMPD2 gene on chromosome 1p13.

Synonyms:  hereditary spastic paraplegia 63,  DOID:0110814,  familial spastic paraplegia 63,  autosomal recessive spastic paraplegia 63,  spastic paraplegia 63 ...