219700.6

Country

Lebanon

HPO Terms

Abnormality of the respiratory system; Failure to thrive; Abnormality of the digestive system; Recurrent upper respiratory tract infections; Exocrine pancreatic insufficiency
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Sex

Male

Family History

Yes

Parental Consanguinity

Yes

Subject Variants

Variant NameAllele CountAllele FrequencyAssociated DiseaseAssociated Gene
NM_000492.4:c.1520_1522del2NA

Remarks

Patient from family '245' in the publication
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