BRD9 gene related symptoms and diseases
All the information presented here about the BRD9 gene and its related diseases, symptoms, and test panels has been aggregated from the following public sources: HGNC,NCBIGENE, Mendelian Rare Disease Search Engine.
Top 5 symptoms and clinical features associated to BRD9 gene
Symptoms // Phenotype | % Cases |
---|---|
Neoplasm | Very Common - Between 80% and 100% cases |
Lymphadenopathy | Very Common - Between 80% and 100% cases |
Abnormal immunoglobulin level | Very Common - Between 80% and 100% cases |
Abnormal lymphocyte morphology | Very Common - Between 80% and 100% cases |
T-cell lymphoma | Very Common - Between 80% and 100% cases |
Other less frequent symptoms and clinical features
Patients with BRD9 gene alterations may also develop some of the following symptoms and phenotypes:Commonly - More than 50% cases
- Lichenification
- Abnormality of the pleura
- Gangrene
- Irregular hyperpigmentation
- Erythroderma
- Ectropion
- Neoplasm of the skin
- Thickened skin
And 21 more phenotypes, you can get all of them using our tools for rare diseases.
Rare diseases associated to BRD9 gene
Here you will find a list of rare diseases related to the BRD9. You can also use our tool to get a more accurate diagnosis based on your current symptoms.
SÉZARY SYNDROME
Alternate names
SÉZARY SYNDROME Is also known as sÉzary lymphoma
Description
Sézary syndrome (SS) is an aggressive form of cutaneous T-cell lymphoma characterized by a triad of erythroderma, lymphadenopathy and circulating atypical lymphocytes (Sézary cells).
Most common symptoms of SÉZARY SYNDROME
- Neoplasm
- Abnormal facial shape
- Peripheral neuropathy
- Hepatomegaly
- Fever
More info about SÉZARY SYNDROME
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