Retinal disordersGene: CTSD
CTSD rated as Green as has a relevant phenotype to be included on the panel following discussion in Genomics England Clinical Team Meeting, 7th October 2019.
Created: 7 Oct 2019, 4:05 p.m. | Last Modified: 7 Oct 2019, 4:05 p.m.
Panel Version: 1.175
Mode of inheritance
BIALLELIC, autosomal or pseudoautosomal
Ceroid lipofuscinosis, neuronal, 10, 610127
overlapping phenotype - CLN
Created: 30 Aug 2019, 2:12 p.m. | Last Modified: 30 Aug 2019, 2:12 p.m.
Panel Version: 1.159
Phenotypes for gene: CTSD were changed from Eye Disorders to Eye Disorders; Ceroid lipofuscinosis, neuronal, 10, 610127
Mode of inheritance for gene: CTSD was changed from to BIALLELIC, autosomal or pseudoautosomal
Gene: ctsd has been classified as Green List (High Evidence).
Source NHS GMS was added to CTSD.
CTSD was added to Posterior segment abnormalitiespanel. Sources: Expert Review Red
CTSD was created by ellenmcdonagh