615510.1

Country

United Arab Emirates

HPO Terms

Episodic vomiting; Achalasia; Global developmental delay; Failure to thrive; Short stature; Generalized hypotonia; Strabismus; Alacrima; Abnormal facial shape
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Sex

Male

Family History

No

Parental Consanguinity

Yes

Subject Variants

Variant NameAllele CountAllele FrequencyAssociated DiseaseAssociated Gene
NM_013335.4:c.922G>A2
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