236792.3.1

Country

Lebanon

HPO Terms

Global developmental delay; Hypothyroidism
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Sex

Male

Family History

Yes

Parental Consanguinity

Yes

Subject Variants

Variant NameAllele CountAllele FrequencyAssociated DiseaseAssociated Gene
NM_024884.2:c.164G>A1NA
NM_024884.2:c.1115delT1NA

Remarks

Patient from family 'F6' in the publication

Related Subjects

Subject IdCountryHPO TermsSexFamily HistoryParental ConsanguinityRemarks
236792.3.2LebanonGlobal developmental delay; HypothyroidismFemaleYesYesPatient from family 'F6' in the publication, sister of 236792.3.1
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