Disease-gene associations mined from literature

Human genes for retinitis pigmentosa-deafness syndrome

Retinitis pigmentosa-deafness syndrome [DOID:0110829]

An Usher syndrome characterized by retinitis pigmentosa and onset of sensorineural hearing impairment in the teens that has_material_basis_in mutation in the MTTS2 gene in the mitochondrial genome.

Synonyms:  retinitis pigmentosa-deafness syndrome,  DOID:0110829,  retinitis pigmentosadeafness syndrome,  retinitis pigmentosa-deafness disease,  retinitis pigmentosa-deafness disorder ...