|
(HPO:0000510) | Rod-cone dystrophy | 266 / 7739 | ||||
|
(HPO:0008527) | Congenital sensorineural hearing impairment | 165 / 7739 | ||||
|
(OMIM) | Hearing loss, congenital sensorineural, moderate-severe | 2 / 7739 | ||||
|
(OMIM) | Progressive retinitis pigmentosa | 4 / 7739 | ||||
|
(HPO:0000007) | Autosomal recessive inheritance | 2538 / 7739 |