RB1CC1 gene related symptoms and diseases
All the information presented here about the RB1CC1 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 RB1CC1 gene
Symptoms // Phenotype | % Cases |
---|---|
Neoplasm | Very Common - Between 80% and 100% cases |
Pain | Very Common - Between 80% and 100% cases |
Carcinoma | Very Common - Between 80% and 100% cases |
Gynecomastia | Very Common - Between 80% and 100% cases |
Breast carcinoma | Very Common - Between 80% and 100% cases |
Other less frequent symptoms and clinical features
Patients with RB1CC1 gene alterations may also develop some of the following symptoms and phenotypes:Commonly - More than 50% cases
- Sarcoma
- Ovarian neoplasm
- Prostate cancer
- Retinoblastoma
- Neoplasm of the breast
- Soft tissue sarcoma
- Endometrial carcinoma
Rare diseases associated to RB1CC1 gene
Here you will find a list of rare diseases related to the RB1CC1. You can also use our tool to get a more accurate diagnosis based on your current symptoms.
BREAST CANCER
Alternate names
BREAST CANCER Is also known as breast cancer, familial
Description
Breast cancer (referring to mammary carcinoma, not mammary sarcoma) is histopathologically and almost certainly etiologically and genetically heterogeneous. Important genetic factors have been indicated by familial occurrence and bilateral involvement.
Most common symptoms of BREAST CANCER
- Neoplasm
- Pain
- Carcinoma
- Gynecomastia
- Breast carcinoma
More info about BREAST CANCER
Search interest in RB1CC1
Potential gene panels for RB1CC1 gene
RB1CC1 Panel
By Fulgent Genetics Fulgent Genetics
This panel specifically test the RB1CC1 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 MYLK IQSEC2 HFE MAP3K7 HLA-DQB1 NPRL3 GBA