TACSTD2 gene related symptoms and diseases
All the information presented here about the TACSTD2 gene and its related diseases, symptoms, and test panels has been aggregated from the following public sources: HGNC,OMIM,ORPHANET,NCBIGENE, Mendelian Rare Disease Search Engine.
Top 5 symptoms and clinical features associated to TACSTD2 gene
| Symptoms // Phenotype | % Cases |
|---|---|
| Cataract | Very Common - Between 80% and 100% cases |
| Visual impairment | Very Common - Between 80% and 100% cases |
| Blindness | Very Common - Between 80% and 100% cases |
| Reduced visual acuity | Very Common - Between 80% and 100% cases |
| Photophobia | Very Common - Between 80% and 100% cases |
Other less frequent symptoms and clinical features
Patients with TACSTD2 gene alterations may also develop some of the following symptoms and phenotypes:Commonly - More than 50% cases
- Corneal dystrophy
- Blurred vision
- Amyloidosis
- Lattice corneal dystrophy
Rare diseases associated to TACSTD2 gene
Here you will find a list of rare diseases related to the TACSTD2. You can also use our tool to get a more accurate diagnosis based on your current symptoms.
GELATINOUS DROP-LIKE CORNEAL DYSTROPHY
Alternate names
GELATINOUS DROP-LIKE CORNEAL DYSTROPHY Is also known as gdcd, amyloidosis, corneal, corneal dystrophy, lattice type iii, amyloid corneal dystrophy, japanese type, lattice corneal dystrophy, type iii, subepithelial amyloidosis of the cornea, primary familial amyloidosis of the cornea, cdgdl
Description
Gelatinous drop-like corneal dystrophy (GDCD) is a form of superficial corneal dystrophy characterized by multiple prominent milky-white gelatinous nodules beneath the corneal epithelium, and marked visual impairment.
Most common symptoms of GELATINOUS DROP-LIKE CORNEAL DYSTROPHY
- Cataract
- Visual impairment
- Blindness
- Reduced visual acuity
- Photophobia
More info about GELATINOUS DROP-LIKE CORNEAL DYSTROPHY
Search interest in TACSTD2
Potential gene panels for TACSTD2 gene
TACSTD2 Panel
Germany.
By Institute for Human Genetics University Clinic Freiburg
This panel specifically test the TACSTD2 gene.
More info about this panel Germany.
Hereditary amyloidosis (NGS panel of 19 genes) Panel
Portugal.
By CGC Genetics Hereditary amyloidosis (NGS panel of 19 genes) that also includes the following genes: TACSTD2 TGFBI TNFRSF1A TTR NLRP3 IL31RA CST3 F10 FGA GSN
More info about this panel Portugal.
Hereditary amyloidosis (NGS panel of 19 genes) Panel
Portugal.
By CGC Genetics Hereditary amyloidosis (NGS panel of 19 genes) that also includes the following genes: TACSTD2 TGFBI TNFRSF1A TTR NLRP3 IL31RA CST3 F10 FGA GSN
More info about this panel Portugal.
Corneal Dystrophies Sequencing Panel with CNV Detection Panel
United States.
By PreventionGenetics PreventionGenetics Corneal Dystrophies Sequencing Panel with CNV Detection that also includes the following genes: TACSTD2 TCF4 ZEB1 TGFBI VSX1 OVOL2 SLC4A11 COL8A2 CYP4V2 ZNF469
More info about this panel United States.
Gelatinous Drop-Like Corneal Dystrophy (GDLD) via TACSTD2 Gene Sequencing with CNV Detection Panel
United States.
By PreventionGenetics PreventionGenetics
This panel specifically test the TACSTD2 gene.
More info about this panel United States.
Eye Diseases - panels Panel
Germany.
By MGZ Medical Genetics Center Eye Diseases - panels that also includes the following genes: BFSP1 BFSP2 SALL2 BMP4 BMP7 SHH SIX3 SIX6 FOXL2 SOX2
More info about this panel Germany.
Corneal Dystrophy Panel
Estonia.
By Asper Biogene Asper Biogene LLC Corneal Dystrophy that also includes the following genes: SOD1 TACSTD2 TCF4 ZEB1 TGFBI VSX1 SLC4A11 COL17A1 COL8A2 CYP4V2
More info about this panel Estonia.
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.
TACSTD2 Panel
United States.
By Fulgent Genetics Fulgent Genetics
This panel specifically test the TACSTD2 gene.
More info about this panel United States.
Corneal Dystrophy Panel Panel
Finland.
By Blueprint Genetics Corneal Dystrophy Panel that also includes the following genes: TACSTD2 TCF4 ZEB1 TGFBI OVOL2 SLC4A11 COL17A1 COL5A1 COL8A2 CYP4V2
More info about this panel Finland.
AMYLOIDOSIS HEREDITARY NGS PANEL Panel
Spain.
By Laboratorio de Genetica Clinica SL AMYLOIDOSIS HEREDITARY NGS PANEL that also includes the following genes: TACSTD2 TGFBI TNFRSF1A TTR NLRP3 IL31RA CST3 F10 FGA GSN
More info about this panel Spain.
Corneal Dystrophy , Panel Massive Sequencing (NGS) 18 Genes Panel
Spain.
By Reference Laboratory Genetics Corneal Dystrophy , Panel Massive Sequencing (NGS) 18 Genes that also includes the following genes: TACSTD2 TCF4 ZEB1 TGFBI VSX1 SLC4A11 COL5A1 COL8A2 CYP4V2 ZNF469
More info about this panel Spain.
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