DISEASES

Disease-gene associations mined from literature

Human genes for hereditary spastic paraplegia 76

Hereditary spastic paraplegia 76 [DOID:0110821]

A hereditary spastic paraplegia that has_material_basis_in mutation in the CAPN1 gene on chromosome 11q13.

Synonyms:  hereditary spastic paraplegia 76,  DOID:0110821,  familial spastic paraplegia 76,  SPG76,  autosomal recessive spastic paraplegia 76