601536.8.1

Country

Saudi Arabia

HPO Terms

Hearing impairment; Global developmental delay; Seizure; Tetralogy of Fallot; Low-set ears; Hypertrichosis; Talipes equinovarus
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Sex

Male

Family History

Yes

Parental Consanguinity

Yes

Subject Variants

Variant NameAllele CountAllele FrequencyAssociated DiseaseAssociated Gene
NM_005522.5:c.175dup2

Remarks

'Patient C1' in the publication

Related Subjects

Subject IdCountryHPO TermsSexFamily HistoryParental ConsanguinityRemarks
601536.8.2Saudi ArabiaHearing impairment; Talipes equinovarus; Global developmental delay; Ventricular septal defectFemaleYesYesSister of 601538.8.1
601536.8.3Saudi ArabiaCongestive heart failure; Ventricular septal defectFemaleYesYesSister of 601538.8.1
601536.8.4Saudi ArabiaVentricular septal defectMaleYesYesBrother of 601538.8.1
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