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(HPO:0000510) | Rod-cone dystrophy | 266 / 7739 | ||||
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(HPO:0001756) | Vestibular hypofunction | 3 / 7739 | ||||
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(HPO:0008527) | Congenital sensorineural hearing impairment | 165 / 7739 | ||||
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(OMIM) | Hearing loss, profound congenital sensorineural | 3 / 7739 | ||||
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(OMIM) | Progressive retinitis pigmentosa | 4 / 7739 | ||||
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(OMIM) | Retinitis pigmentosa, sector type (in some patients) | 1 / 7739 | ||||
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(HPO:0000007) | Autosomal recessive inheritance | 2538 / 7739 |