600791.6.1

Country

United Arab Emirates

HPO Terms

Sensorineural hearing impairment
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Sex

Male

Family History

Yes

Parental Consanguinity

Yes

Subject Variants

Variant NameAllele CountAllele FrequencyAssociated DiseaseAssociated Gene
NM_000441.2:c.716T>A2

Remarks

Patient from 'family 3' in the publication

References

Related Subjects

Subject IdCountryHPO TermsSexFamily HistoryParental ConsanguinityRemarks
600791.6.2United Arab EmiratesSensorineural hearing impairmentMaleYesNoFather of 600791.6.1
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