612674.1.1

Country

Lebanon

HPO Terms

Sensorineural hearing impairment; Rod-cone dystrophy; Cataract; Ataxia
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Sex

Female

Family History

Yes

Parental Consanguinity

Yes

Subject Variants

Variant NameAllele CountAllele FrequencyAssociated DiseaseAssociated Gene
NM_001042472.3:c.193C>T2

Related Subjects

Subject IdCountryHPO TermsSexFamily HistoryParental ConsanguinityRemarks
612674.1.2LebanonSensorineural hearing impairment; Rod-cone dystrophy; Cataract; AtaxiaMaleYesYesBrother of 612674.1.1
612674.1.3LebanonMaleYesUnaffected father of 612674.1.1
612674.1.4LebanonFemaleYesUnaffected mother of 612674.1.1
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