KRT3 gene related symptoms and diseases
All the information presented here about the KRT3 gene and its related diseases, symptoms, and test panels has been aggregated from the following public sources: NCBIGENE,OMIM,HGNC,ORPHANET, Mendelian Rare Disease Search Engine.
Top 5 symptoms and clinical features associated to KRT3 gene
| Symptoms // Phenotype | % Cases |
|---|---|
| Neoplasm | Uncommon - Between 30% and 50% cases |
| Corneal opacity | Uncommon - Between 30% and 50% cases |
| Frontal balding | Uncommon - Between 30% and 50% cases |
| Hypopnea | Uncommon - Between 30% and 50% cases |
| Conjunctival hyperemia | Uncommon - Between 30% and 50% cases |
Other less frequent symptoms and clinical features
Patients with KRT3 gene alterations may also develop some of the following symptoms and phenotypes:Not very common - Between 30% and 50% cases
- Enlarged ovaries
- Beta-cell dysfunction
- Pain
- Reduced visual acuity
- Photophobia
- Scarring
- Astigmatism
- Prostate cancer
And 35 more phenotypes, you can get all of them using our tools for rare diseases.
Rare diseases associated to KRT3 gene
Here you will find a list of rare diseases related to the KRT3. You can also use our tool to get a more accurate diagnosis based on your current symptoms.
POLYCYSTIC OVARY SYNDROME 1; PCOS1
Alternate names
POLYCYSTIC OVARY SYNDROME 1; PCOS1 Is also known as pco, pco1, hyperandrogenemia, stein-leventhal syndrome, pcos
Description
a health problem that can affect a woman's menstrual cycle, fertility, hormones, insulin production, heart, blood vessels, and appearance
Most common symptoms of POLYCYSTIC OVARY SYNDROME 1; PCOS1
- Neoplasm
- Abnormality of metabolism/homeostasis
- Obesity
- Diabetes mellitus
- Apnea
More info about POLYCYSTIC OVARY SYNDROME 1; PCOS1
MEESMANN CORNEAL DYSTROPHY
Alternate names
MEESMANN CORNEAL DYSTROPHY Is also known as mecd, juvenile hereditary epithelial dystrophy of meesmann, meesmann corneal dystrophy, corneal dystrophy, meesmann epithelial, corneal dystrophy, juvenile epithelial, of meesmann
Description
Meesmann corneal dystrophy (MECD) is a rare form of superficial corneal dystrophy characterized by distinct tiny bubble-like, round-to-oval punctate bilateral opacities in the central corneal epithelium, and to a lesser extent in the peripheral cornea, with little impact on vision.
Most common symptoms of MEESMANN CORNEAL DYSTROPHY
- Pain
- Reduced visual acuity
- Photophobia
- Scarring
- Corneal opacity
More info about MEESMANN CORNEAL DYSTROPHY
Search interest in KRT3
Potential gene panels for KRT3 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.
KRT3 Panel
Germany.
By Institute for Human Genetics University Clinic Freiburg
This panel specifically test the KRT3 gene.
More info about this panel Germany.
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.
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.
Meesmann corneal dystrophy: KRT3 gene sequence analysis Panel
Spain.
By GENETAQ Molecular Genetics Centre and Diagnosis of Rare Diseases
This panel specifically test the KRT3 gene.
More info about this panel Spain.
KRT3 Panel
United States.
By Fulgent Genetics Fulgent Genetics
This panel specifically test the KRT3 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.
Meesmann Corneal Distrophy , Sequencing KRT3 Gene Panel
Spain.
By Reference Laboratory Genetics
This panel specifically test the KRT3 gene.
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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