LACC1 gene related symptoms and diseases
All the information presented here about the LACC1 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 LACC1 gene
Symptoms // Phenotype | % Cases |
---|---|
Visual impairment | Very Common - Between 80% and 100% cases |
Falls | Very Common - Between 80% and 100% cases |
Anterior uveitis | Very Common - Between 80% and 100% cases |
Elevated C-reactive protein level | Very Common - Between 80% and 100% cases |
Juvenile rheumatoid arthritis | Very Common - Between 80% and 100% cases |
Other less frequent symptoms and clinical features
Patients with LACC1 gene alterations may also develop some of the following symptoms and phenotypes:Commonly - More than 50% cases
- Joint swelling
- Uveitis
- Pericarditis
- Elevated erythrocyte sedimentation rate
- Rheumatoid arthritis
- Pleural effusion
- Lymphadenopathy
- Hepatomegaly
And 11 more phenotypes, you can get all of them using our tools for rare diseases.
Rare diseases associated to LACC1 gene
Here you will find a list of rare diseases related to the LACC1. You can also use our tool to get a more accurate diagnosis based on your current symptoms.
SYSTEMIC-ONSET JUVENILE IDIOPATHIC ARTHRITIS
Alternate names
SYSTEMIC-ONSET JUVENILE IDIOPATHIC ARTHRITIS Is also known as systemic-onset jia, systemic juvenile rheumatoid arthritis, still disease, systemic polyarthritis
Description
Systemic-onset juvenile idiopathic arthritis is marked by the severity of the extra-articular manifestations (fever, cutaneous eruptions) and by an equal sex ratio.
Most common symptoms of SYSTEMIC-ONSET JUVENILE IDIOPATHIC ARTHRITIS
- Visual impairment
- Hepatomegaly
- Fever
- Splenomegaly
- Visual loss
More info about SYSTEMIC-ONSET JUVENILE IDIOPATHIC ARTHRITIS
Search interest in LACC1
Potential gene panels for LACC1 gene
LACC1 Panel
By Fulgent Genetics Fulgent Genetics
This panel specifically test the LACC1 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 CTRC RPS6KA3 OTOG ADCY5 PSENEN ATXN7 GNPTAB