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(HPO:0001756) | Vestibular hypofunction | rare [HPO:skoehler] | 3 / 7739 | |||
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(OMIM) | Deafness, congenital nonprogressive sensorineural symmetric, moderate | 1 / 7739 | ||||
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(HPO:0000007) | Autosomal recessive inheritance | 2538 / 7739 | ||||
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(HPO:0000365) | Hearing impairment | 539 / 7739 |