Retinal disorders
Gene: CTSDEnsemblGeneIds (GRCh38): ENSG00000117984
EnsemblGeneIds (GRCh37): ENSG00000117984
OMIM: 116840, Gene2Phenotype
CTSD is in 12 panels
2 reviews
Catherine Snow (Genomics England)
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
Phenotypes
Ceroid lipofuscinosis, neuronal, 10, 610127
Gavin Arno (UCL Institute of Ophthalmology/Moorfields Eye Hospital)
overlapping phenotype - CLNCreated: 30 Aug 2019, 2:12 p.m. | Last Modified: 30 Aug 2019, 2:12 p.m.
Panel Version: 1.159
Details
- Mode of Inheritance
- BIALLELIC, autosomal or pseudoautosomal
- Sources
-
- Expert Review Green
- NHS GMS
- Phenotypes
-
- Eye Disorders
- Ceroid lipofuscinosis, neuronal, 10, 610127
- OMIM
- 116840
- Clinvar variants
- Variants in CTSD
- Penetrance
- Complete
- Panels with this gene
-
- Structural eye disease
- Early onset or syndromic epilepsy
- Fetal anomalies
- Glaucoma (developmental)
- Undiagnosed metabolic disorders
- Lysosomal storage disorder
- Intellectual disability
- Childhood onset dystonia, chorea or related movement disorder
- Likely inborn error of metabolism
- Retinal disorders
- DDG2P
- Neuronal ceroid lipofuscinosis
History Filter Activity
Set Phenotypes
Catherine Snow (Genomics England)Phenotypes for gene: CTSD were changed from Eye Disorders to Eye Disorders; Ceroid lipofuscinosis, neuronal, 10, 610127
Set mode of inheritance
Catherine Snow (Genomics England)Mode of inheritance for gene: CTSD was changed from to BIALLELIC, autosomal or pseudoautosomal
Entity classified by Genomics England curator
Catherine Snow (Genomics England)Gene: ctsd has been classified as Green List (High Evidence).
Added New Source
Ivone Leong (Genomics England Curator)Source NHS GMS was added to CTSD.
Added New Source
Ellen McDonagh (Genomics England Curator)CTSD was added to Posterior segment abnormalitiespanel. Sources: Expert Review Red
Created
Ellen McDonagh (Genomics England Curator)CTSD was created by ellenmcdonagh