617781.5

Country

Saudi Arabia

HPO Terms

Visual impairment; Nystagmus; Oculodigital reflex; Global developmental delay; Short finger; Hypotonia;
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Sex

Female

Family History

No

Parental Consanguinity

Yes

Subject Variants

Variant NameAllele CountAllele FrequencyAssociated DiseaseAssociated Gene
NM_014714.4:c.1990G>A2
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