613835.6.2

Syria

Macular atrophy; Foveal atrophy

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Male

Yes

Yes

Variant Name	Allele Count	Allele Frequency	Associated Disease	Associated Gene
NM_201253.3:c.2555T>C	2		Leber Congenital Amaurosis 8

Sibling of 613835.6.1

Related Subjects

Subject Id	Country	HPO Terms	Sex	Family History	Parental Consanguinity	Remarks
613835.6.1	Syria	Retinal dystrophy; Rod-cone dystrophy	Female	Yes	Yes

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