242840.6

Country

Oman

HPO Terms

Agenesis of corpus callosum; Cataract; Pallor; Cardiomyopathy; Profound global developmental delay; Failure to thrive; Microcephaly
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Family History

Yes

Parental Consanguinity

Yes

Subject Variants

Variant NameAllele CountAllele FrequencyAssociated DiseaseAssociated Gene
NM_020964.3:c.6084G>A2

Remarks

The patient has a similarly affected sibling
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