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 ...