600974.3.2

Country

Morocco

HPO Terms

Hearing impairment
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Sex

Male

Family History

Yes

Parental Consanguinity

No

Subject Variants

Variant NameAllele CountAllele FrequencyAssociated DiseaseAssociated Gene
NM_138691.2:c.1939T>C2

Remarks

Brother of 600974.3.1

Related Subjects

Subject IdCountryHPO TermsSexFamily HistoryParental ConsanguinityRemarks
600974.3.1MoroccoHearing impairmentFemaleYesNo
600974.3.3MoroccoMaleYesNoUnaffected father of 600974.3.1
600974.3.4MoroccoFemaleYesNoUnaffected mother of 600974.3.1
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