DISEASES

Disease-gene associations mined from literature

Human genes for hereditary spastic paraplegia 18

Hereditary spastic paraplegia 18 [DOID:0110771]

A hereditary spastic paraplegia that has_material_basis_in mutation in the ERLIN2 gene on chromosome 8p11.

Synonyms:  hereditary spastic paraplegia 18,  DOID:0110771,  familial spastic paraplegia 18,  IDMDC,  SPG18 ...