220290.G.7.3

Country

Palestine

HPO Terms

Profound hearing impairment
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Sex

Unknown

Family History

Yes

Parental Consanguinity

Yes

Subject Variants

Variant NameAllele CountAllele FrequencyAssociated DiseaseAssociated Gene
NM_004004.5:c.35del1NA
NM_004004.5:c.229T>C1NA

Remarks

Unknown number of compound heterozygous patients in a group of 51 affected individuals

Related Subjects

Subject IdCountryHPO TermsSexFamily HistoryParental ConsanguinityRemarks
220290.G.7.1PalestineProfound hearing impairmentUnknownYesYesUnknown number of patients in a group of 51 affected individuals
220290.G.7.2PalestineProfound hearing impairmentUnknownYesYesUnknown number of patients in a group of 51 affected individuals
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