Retinal disordersGene: LZTFL1
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, 8:04 a.m.
Source NHS GMS was added to LZTFL1. Rating Changed from Green List (high evidence) to Green List (high evidence)
Phenotypes for LZTFL1 were set to Eye Disorders; Bardet-Biedl syndrome 17
Mode of inheritance for LZTFL1 was changed to BIALLELIC, autosomal or pseudoautosomal
LZTFL1 was added to Posterior segment abnormalitiespanel. Sources: Expert Review Green
LZTFL1 was created by ellenmcdonagh