TNRC6B gene related symptoms and diseases
All the information presented here about the TNRC6B gene and its related diseases, symptoms, and test panels has been aggregated from the following public sources: OMIM,NCBIGENE,HGNC, Mendelian Rare Disease Search Engine.
Top 5 symptoms and clinical features associated to TNRC6B gene
Symptoms // Phenotype | % Cases |
---|---|
Neoplasm | Very Common - Between 80% and 100% cases |
Alopecia of scalp | Very Common - Between 80% and 100% cases |
Enlarged ovaries | Very Common - Between 80% and 100% cases |
Conjunctival hyperemia | Very Common - Between 80% and 100% cases |
Hypopnea | Very Common - Between 80% and 100% cases |
Other less frequent symptoms and clinical features
Patients with TNRC6B gene alterations may also develop some of the following symptoms and phenotypes:Commonly - More than 50% cases
- Frontal balding
- Enlarged polycystic ovaries
- Prostate cancer
- Menstrual irregularities
- Abnormality of the ovary
- Adrenal hyperplasia
- Prolactin excess
- Increased reactive oxygen species production
And 19 more phenotypes, you can get all of them using our tools for rare diseases.
Rare diseases associated to TNRC6B gene
Here you will find a list of rare diseases related to the TNRC6B. 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
Search interest in TNRC6B
Potential gene panels for TNRC6B gene
Autism Spectrum Disorders Sequencing Panel with CNV Detection Panel
By PreventionGenetics PreventionGenetics Autism Spectrum Disorders Sequencing Panel with CNV Detection that also includes the following genes: SCN1A SCN2A SGSH BRAF SLC6A1 SLC9A6 SPAST CDKL5 STXBP1 SYN2
More info about this panelTNRC6B Panel
By Fulgent Genetics Fulgent Genetics
This panel specifically test the TNRC6B gene.
More info about this panelIf you liked this article maybe you will also find interesting the following in-depth articles about other rare diseases, like SPECC1L VAMP1 BMPR1B SYNE2 EBP HNRNPH2 MMAA