620747.1.1

Egypt

Intellectual disability, mild

Male

Yes

Yes

Variant Name	Allele Count	Allele Frequency	Associated Disease	Associated Gene
NM_001013663.2:c.365G>A	2		Neurodevelopmental Disorder with Early-Onset Parkinsonism and Behavioral Abnormalities

Authors classified this gene variant as a "moderately confident" novel candidate for neurodevelopmental disorders.

Related Subjects

Subject Id	Country	HPO Terms	Sex	Family History	Parental Consanguinity	Remarks
620747.1.2	Egypt	Intellectual disability, mild	Male	Yes	Yes	Relative of 620747.1.1