DISEASES

Disease-gene associations mined from literature

Human genes for hereditary spastic paraplegia 49

Hereditary spastic paraplegia 49 [DOID:0110801]

A hereditary spastic paraplegia that has_material_basis_in mutation in the TECPR2 gene on chromosome 14q32.

Synonyms:  hereditary spastic paraplegia 49,  DOID:0110801,  familial spastic paraplegia 49,  SPG49,  autosomal recessive spastic paraplegia 49 ...