163950.2

Country

Lebanon

HPO Terms

Intellectual disability; Global developmental delay; Abnormal heart morphology; Cryptorchidism; Low-set ears
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Sex

Male

Parental Consanguinity

No

Subject Variants

Variant NameAllele CountAllele FrequencyAssociated DiseaseAssociated Gene
NM_002834.5:c.1510A>G1
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