615905.1

Country

Saudi Arabia

HPO Terms

Microcephaly; Seizure; Hypotonia; Severe global developmental delay
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Sex

Male

Family History

Yes

Parental Consanguinity

Yes

Subject Variants

Variant NameAllele CountAllele FrequencyAssociated DiseaseAssociated Gene
NM_177550.5:c.1227dup2
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