type 9 Amaurosis congenita of Leber

Also Known As:

Amaurosis congenita of Leber, type 9; Leber Congenital Amaurosis 9; Leber congenital amaurosis, type 9

Networked: 2 relevant articles (0 outcomes, 0 trials/studies)

1.	Retinal Degeneration

Drugs and Important Biological Agents (IBA) related to type 9 Amaurosis congenita of Leber:

1.	Protein Isoforms (Isoforms)IBA 01/01/2023 - "Mutations in the nuclear-specific isoform, NMNAT1, have been extensively reported as the cause of Leber congenital amaurosis-type 9 (LCA9). "
2.	NAD (NADH)IBA 07/10/2015 - "Leber congenital amaurosis 9 (LCA9) is an autosomal recessive retinal degeneration condition caused by mutations in the NAD(+) biosynthetic enzyme NMNAT1. "
3.	EnzymesIBA 07/10/2015 - "Leber congenital amaurosis 9 (LCA9) is an autosomal recessive retinal degeneration condition caused by mutations in the NAD(+) biosynthetic enzyme NMNAT1. "