601631.1.5

Country

Lebanon

HPO Terms

;

Subject Variants

Variant NameAllele CountAllele FrequencyAssociated DiseaseAssociated Gene
NM_001453.3:c.379C>T1

Remarks

Mother of 601631.1.1

Related Subjects

Subject IdCountryHPO TermsSexFamily HistoryParental ConsanguinityRemarks
601631.1.1LebanonPrimary congenital glaucoma; Aniridia; Ventricular septal defectFemaleYesYes
601631.1.2LebanonPrimary congenital glaucoma; AniridiaMaleYesYesSibling of 601631.1.1
601631.1.3LebanonPrimary congenital glaucoma; Aniridia; Congestive heart failure; ventricular septal defect;FemaleYesYesSibling of 601631.1.1
601631.1.4Lebanon;MaleFather of 601631.1.1
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