261600.9

Country

Lebanon

HPO Terms

Hyperphenylalaninemia; Severe global developmental delay; Seizure; Nausea; Vomiting
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Sex

Unknown

Family History

No

Parental Consanguinity

Yes

Subject Variants

Variant NameAllele CountAllele FrequencyAssociated DiseaseAssociated Gene
NM_000277.3:c.1066-11G>A2
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