615009.1

Country

United Arab Emirates

HPO Terms

Global developmental delay; Seizure; Intellectual disability; Abnormal heart morphology
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Sex

Male

Family History

No

Parental Consanguinity

Yes

Subject Variants

Variant NameAllele CountAllele FrequencyAssociated DiseaseAssociated Gene
NM_018026.3:c.607C>T1

Remarks

de novo mutation

Related Subjects

Subject IdCountryHPO TermsSexFamily HistoryParental ConsanguinityRemarks
615009.2United Arab EmiratesGlobal developmental delayFemaleNoNode novo mutation
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