TP73 gene related symptoms and diseases
All the information presented here about the TP73 gene and its related diseases, symptoms, and test panels has been aggregated from the following public sources: HGNC,ORPHANET,OMIM,NCBIGENE, Mendelian Rare Disease Search Engine.
Top 5 symptoms and clinical features associated to TP73 gene
Symptoms // Phenotype | % Cases |
---|---|
Neoplasm | Very Common - Between 80% and 100% cases |
Carcinoma | Very Common - Between 80% and 100% cases |
Subcutaneous nodule | Very Common - Between 80% and 100% cases |
Neoplasm of the lung | Very Common - Between 80% and 100% cases |
Retinoblastoma | Very Common - Between 80% and 100% cases |
Other less frequent symptoms and clinical features
Patients with TP73 gene alterations may also develop some of the following symptoms and phenotypes:Commonly - More than 50% cases
- Small cell lung carcinoma
Rare diseases associated to TP73 gene
Here you will find a list of rare diseases related to the TP73. You can also use our tool to get a more accurate diagnosis based on your current symptoms.
SMALL CELL LUNG CANCER
Alternate names
SMALL CELL LUNG CANCER Is also known as sclc, sccl, sclc1
Description
Small cell lung cancer (SCLC) is a highly aggressive malignant neoplasm, accounting for 10-15% of lung cancer cases, characterized byrapid growth, and early metastasis. SCLC usually manifests as a large hilar mass with bulky mediastinal lymphadenopathy presenting clinically with chest pain, persistent cough, dyspnea, wheezing, hoarseness, hemoptysis, loss of appetite, weight loss, and neurological and endocrine paraneoplastic syndromes. SCLC is primarily reported in elderly people with a history of long-term tobacco exposure.
Most common symptoms of SMALL CELL LUNG CANCER
- Neoplasm
- Carcinoma
- Subcutaneous nodule
- Neoplasm of the lung
- Retinoblastoma
More info about SMALL CELL LUNG CANCER
Search interest in TP73
Potential gene panels for TP73 gene
TP73 Panel
By Fulgent Genetics Fulgent Genetics
This panel specifically test the TP73 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 HLX-AS1 CHD7 BPGM DBH FH KDM1A MYO1E