607200.1.1

Country

Oman

HPO Terms

Congenital hypothyroidism
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Sex

Male

Parental Consanguinity

Yes

Subject Variants

Variant NameAllele CountAllele FrequencyAssociated DiseaseAssociated Gene
NM_001363711.1:c.3082_3085delinsGCTTCCT2

Related Subjects

Subject IdCountryHPO TermsSexFamily HistoryParental ConsanguinityRemarks
607200.1.2OmanMale
607200.1.3OmanMale
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