275900.2

Country

Oman

HPO Terms

Global developmental delay; Microcephaly; Failure to thrive; Ataxia; Dysarthria; Strabismus
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Sex

Unknown

Family History

Yes

Parental Consanguinity

Yes

Subject Variants

Variant NameAllele CountAllele FrequencyAssociated DiseaseAssociated Gene
NM_015087.5:c.1450dup2
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