Night Blindness, Congenital Stationary, Autosomal Dominant 3; Csnbad3
Genes related to Night Blindness, Congenital Stationary, Autosomal Dominant 3; Csnbad3
- GNAT1
Clinical Features
Phenotypes and symptoms related to Night Blindness, Congenital Stationary, Autosomal Dominant 3; Csnbad3
- Blindness
- Rod-cone dystrophy
- Retinopathy
- Nyctalopia
- Constriction of peripheral visual field
- Congenital stationary night blindness
Incidence and onset information
— Currently we don't have prevalence information about this disease (Not enough data available about incidence and published cases.)— No data available about the known clinical features onset.
Alternative names
Night Blindness, Congenital Stationary, Autosomal Dominant 3; Csnbad3 Is also known as night blindness, congenital stationary, nougaret type.
Researches and researchers
Currently, we don't have any information about doctors, researches or researchers related to this disease. Please contact us if you would like to appear here.Night Blindness, Congenital Stationary, Autosomal Dominant 3; Csnbad3 Recommended genes panels
Panel Name, Specifity and genes Tested/covered |
---|
MitoMet®Plus aCGH Analysis.
By Baylor Miraca Genetics Laboratories (United States).
RGS9, RHO, GRK1, RLBP1, RNASEL, BCS1L, RP1, RP2, RP9, RPE65, RPGR, RPL35A, MRPL3, RPS14, RS1, SAG, SARDH, SCO2, SCP2, SDHB , (...)
View the complete list with 612 more genes
Specificity
1 %
Genes
100 % |
Congenital Stationary Night Blindness Panel.
By Greenwood Genetic Center Diagnostic Laboratories Greenwood Genetic Center (United States).
RHO, GRK1, SAG, SLC24A1, CABP4, CACNA1F, LRIT3, GPR179, GNAT1, GNB3, GRM6, TRPM1, NYX, PDE6B, RDH5
Specificity
7 %
Genes
100 % |
GNAT1.
By Institute for Human Genetics University Clinic Freiburg (Germany).
GNAT1
Specificity
100 %
Genes
100 % |
Night blindness, congenital stationary 3, AD (sequence analysis of GNAT1 gene).
By CGC Genetics (Portugal).
GNAT1
Specificity
100 %
Genes
100 % |
Night blindness, congenital stationary (NGS panel of 13 genes).
By CGC Genetics (Portugal).
RHO, GRK1, SAG, SLC24A1, CACNA1F, LRIT3, GPR179, GNAT1, GNB3, GRM6, TRPM1, NYX, PDE6B
Specificity
8 %
Genes
100 % |
Night blindness, congenital stationary (NGS panel of 13 genes).
By CGC Genetics (Portugal).
RHO, GRK1, SAG, SLC24A1, CACNA1F, LRIT3, GPR179, GNAT1, GNB3, GRM6, TRPM1, NYX, PDE6B
Specificity
8 %
Genes
100 % |
Congenital Stationary Night Blindness Sequencing Panel with CNV Detection.
By PreventionGenetics PreventionGenetics (United States).
RHO, GRK1, RPE65, SAG, SLC24A1, CABP4, CACNA1F, CHM, CACNA2D4, LRIT3, GPR179, GNAT1, GRM6, TRPM1, NYX, PDE6B, RDH5
Specificity
6 %
Genes
100 % |
Comprehensive Inherited Retinal Dystrophies (includes RPGR ORF15) Sequencing Panel with CNV Detection.
By PreventionGenetics PreventionGenetics (United States).
RGS9, RHO, GRK1, RLBP1, ROM1, RP1, RP2, RP9, RPE65, RPGR, RS1, CNNM4, SAG, SDCCAG8, SEMA4A, SLC24A1, SLC4A7, SPP2, PLK4, TEAD1 , (...)
View the complete list with 286 more genes
Specificity
1 %
Genes
100 % |
You can get up to 20 more panels with our dedicated tool
Learn moreSources and references
You can check the following sources for additional information.
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