Leber congenital amaurosis 17

Leber congenital amaurosis 17 is an autosomal recessive disorder caused by mutations of the GDF6 gene.

Systematic

Leber congenital amaurosis
	Leber congenital amaurosis 01
	Leber congenital amaurosis 02
	Leber congenital amaurosis 03
	Leber congenital amaurosis 04
	Leber congenital amaurosis 05
	Leber congenital amaurosis 06
	Leber congenital amaurosis 07
	Leber congenital amaurosis 08
	Leber congenital amaurosis 09
	Leber congenital amaurosis 10
	Leber congenital amaurosis 11
	Leber congenital amaurosis 12
	Leber congenital amaurosis 13
	Leber congenital amaurosis 14
	Leber congenital amaurosis 15
	Leber congenital amaurosis 16
	Leber congenital amaurosis 17
		GDF6
	Leber congenital amaurosis 18

References:

1.	Asai-Coakwell M et al. (2013) Contribution of growth differentiation factor 6-dependent cell survival to early-onset retinal dystrophies.

2.	OMIM.ORG article Omim 615360

Update: June 23, 2025

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