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

SOURCES: MESH ORPHANET OMIM


Potential gene panels for TEAD1 gene

MitoMet®Plus aCGH Analysis Panel

United States.

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 panel
United States.

Comprehensive Inherited Retinal Dystrophies (includes RPGR ORF15) Sequencing Panel with CNV Detection Panel

United States.

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 panel
United States.

Sveinsson choreoretinal atrophy Panel

Germany.

By Centogene AG - the Rare Disease Company

This panel specifically test the TEAD1 gene.

More info about this panel
Germany.

Eye diseases comprehensive panel Panel

Estonia.

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 panel
Estonia.

Retinal Dystrophy Panel Panel

United States.

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 panel
United States.

MVL Vision Panel Panel

United States.

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 panel
United States.

TEAD1 Panel

United States.

By Fulgent Genetics Fulgent Genetics

This panel specifically test the TEAD1 gene.

More info about this panel
United States.

Retinal Dystrophy Panel Panel

Finland.

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 panel
Finland.

Tempus xO assay Panel

United States.

By Tempus Labs, Inc. Tempus xO assay that also includes the following genes: BCL6 RHEB RIPK1 RIPK2 RIPK3 RIT1 BCL7A BCL9 BCR ROBO2

More info about this panel
United States.

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