614228.1

United Arab Emirates

Intellectual disability, mild; Specific learning disability; Attention deficit hyperactivity disorder; Spasticity; Ataxia; Global developmental delay

Male

Yes

Yes

Variant Name	Allele Count	Allele Frequency	Associated Disease	Associated Gene
NM_001376.4:c.752G>A	1		Charcot-Marie-Tooth Disease, Axonal, Type 2O

Affected father