Retinal disordersGene: ADAM9
This gene is on the Manchester Genetic Retinal Degeneration Conditions panel (covers known genes for isolated progessive retinal degeneration, Leber congenital amaurosis, macular dystrophy, achromatopsia, congenital stationary night blindness as well as the two most common causes of syndromic blindess Usher and Bardet-Biedl syndromes and additional syndromes including Joubert, Senior-Loken, and Cohen syndrome.
Created: 2 Jun 2016, 8:03 a.m.
Comment on mode of inheritance: Confirmed on OMIM.
Created: 15 Mar 2016, 9:04 a.m.
Source NHS GMS was added to ADAM9. Rating Changed from Green List (high evidence) to Green List (high evidence)
This gene has been classified as Green List (High Evidence).
Mode of inheritance for ADAM9 was changed to BIALLELIC, autosomal or pseudoautosomal
Model of inheritance for gene ADAM9 was set to BIALLELIC, autosomal or pseudoautosomal
ADAM9 was created by ellenmcdonagh
ADAM9 was added to Posterior segment abnormalitiespanel. Sources: Expert Review Green