201910.35.3

Lebanon

Congenital adrenal hyperplasia; ; ; ;

Female

Yes

Variant Name	Allele Count	Allele Frequency	Associated Disease	Associated Gene
NM_001128590.3:c.754G>T	2		Adrenal Hyperplasia, Congenital, due to 21-Hydroxylase Deficiency

Related Subjects

Subject Id	Country	HPO Terms	Sex	Family History	Parental Consanguinity	Remarks
201910.35.1	Lebanon	Asymptomatic; ; ; ; ;	Male		Yes	Brother of 201910.35.3
201910.35.2	Lebanon	Asymptomatic; ; ; ; ;	Male		Yes	Brother of 201910.35.3