TEAD1 gene related symptoms and diseases
All the information presented here about the TEAD1 gene and its related diseases, symptoms, and test panels has been aggregated from the following public sources: ORPHANET,NCBIGENE,HGNC,OMIM, Mendelian Rare Disease Search Engine.
Top 5 symptoms and clinical features associated to TEAD1 gene
Symptoms // Phenotype | % Cases |
---|---|
Myopia | Very Common - Between 80% and 100% cases |
Abnormality of the eye | Very Common - Between 80% and 100% cases |
Astigmatism | Very Common - Between 80% and 100% cases |
Chorioretinal atrophy | Very Common - Between 80% and 100% cases |
Chorioretinal degeneration | Very Common - Between 80% and 100% cases |
Other less frequent symptoms and clinical features
Patients with TEAD1 gene alterations may also develop some of the following symptoms and phenotypes:Commonly - More than 50% cases
- Peripapillary chorioretinal atrophy
Rare diseases associated to TEAD1 gene
Here you will find a list of rare diseases related to the TEAD1. You can also use our tool to get a more accurate diagnosis based on your current symptoms.
HELICOID PERIPAPILLARY CHORIORETINAL DEGENERATION
Alternate names
HELICOID PERIPAPILLARY CHORIORETINAL DEGENERATION Is also known as aa, scra, sveinsson chorioretinal atrophy, atrophia areata, helicoidal peripapillary chorioretinal degeneration, peripapillary chorioretinal degeneration, icelandic type, hpcd
Description
Helicoid peripapillary chorioretinal degeneration is a rare autosomal dominantly inherited chorioretinal degeneration disease, presenting at birth or infancy, characterized by progressive bilateral retinal and choroidal atrophy, appearing as lesions on the optic nerve and peripheral ocular fundus and leading to central vision loss. Congenital anterior polar cataracts are sometimes associated with this disease.
Most common symptoms of HELICOID PERIPAPILLARY CHORIORETINAL DEGENERATION
- Myopia
- Abnormality of the eye
- Astigmatism
- Chorioretinal atrophy
- Chorioretinal degeneration
More info about HELICOID PERIPAPILLARY CHORIORETINAL DEGENERATION
Search interest in TEAD1
Potential gene panels for TEAD1 gene
MitoMet®Plus aCGH Analysis Panel
By Baylor Miraca Genetics Laboratories MitoMet®Plus aCGH Analysis that also includes the following genes: RGS9 RHO GRK1 RLBP1 RNASEL BCS1L RP1 RP2 RP9 RPE65
More info about this panelComprehensive Inherited Retinal Dystrophies (includes RPGR ORF15) Sequencing Panel with CNV Detection Panel
By PreventionGenetics PreventionGenetics Comprehensive Inherited Retinal Dystrophies (includes RPGR ORF15) Sequencing Panel with CNV Detection that also includes the following genes: RGS9 RHO GRK1 RLBP1 ROM1 RP1 RP2 RP9 RPE65 RPGR
More info about this panelSveinsson choreoretinal atrophy Panel
By Centogene AG - the Rare Disease Company
This panel specifically test the TEAD1 gene.
More info about this panelEye diseases comprehensive panel Panel
By Asper Biogene Asper Biogene LLC Eye diseases comprehensive panel that also includes the following genes: RGS9 RHO GRK1 RLBP1 ROM1 RP1 RP2 RP9 RPE65 RPGR
More info about this panelRetinal Dystrophy Panel Panel
By Molecular Vision Laboratory Retinal Dystrophy Panel that also includes the following genes: RGS9 RHO GRK1 RLBP1 ROM1 RP1 RP2 RP9 RPE65 RPGR
More info about this panelMVL Vision Panel Panel
By Molecular Vision Laboratory MVL Vision Panel that also includes the following genes: RGS9 RHO GRK1 RLBP1 ROM1 RP1 RP2 RP9 RPE65 RPGR
More info about this panelTEAD1 Panel
By Fulgent Genetics Fulgent Genetics
This panel specifically test the TEAD1 gene.
More info about this panelRetinal Dystrophy Panel Panel
By Blueprint Genetics Retinal Dystrophy Panel that also includes the following genes: RGS9 RHO RLBP1 ROM1 RP1 RP2 RPE65 RPGR RS1 CNNM4
More info about this panelTempus xO assay Panel
By Tempus Labs, Inc. Tempus xO assay that also includes the following genes: BCL6 RHEB RIPK1 RIPK2 RIPK3 RIT1 BCL7A BCL9 BCR ROBO2
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