LMO1 gene related symptoms and diseases
All the information presented here about the LMO1 gene and its related diseases, symptoms, and test panels has been aggregated from the following public sources: OMIM,NCBIGENE,HGNC,ORPHANET, Mendelian Rare Disease Search Engine.
Top 5 symptoms and clinical features associated to LMO1 gene
| Symptoms // Phenotype | % Cases |
|---|---|
| Ataxia | Very Common - Between 80% and 100% cases |
| Spinal cord compression | Very Common - Between 80% and 100% cases |
| Elevated urinary homovanillic acid | Very Common - Between 80% and 100% cases |
| Elevated urinary catecholamines | Very Common - Between 80% and 100% cases |
| Elevated urinary dopamine | Very Common - Between 80% and 100% cases |
Other less frequent symptoms and clinical features
Patients with LMO1 gene alterations may also develop some of the following symptoms and phenotypes:Commonly - More than 50% cases
- Abdominal mass
- Opsoclonus
- Adrenal calcification
- Ganglioneuroblastoma
- Horner syndrome
- Neoplasm of the nervous system
- Ganglioneuroma
- Paraganglioma
And 17 more phenotypes, you can get all of them using our tools for rare diseases.
Rare diseases associated to LMO1 gene
Here you will find a list of rare diseases related to the LMO1. You can also use our tool to get a more accurate diagnosis based on your current symptoms.
NEUROBLASTOMA
Description
Neuroblastoma is a malignant tumor of neural crest cells, the cells that give rise to the sympathetic nervous system, which is observed in children.
Most common symptoms of NEUROBLASTOMA
- Ataxia
- Neoplasm
- Failure to thrive
- Pain
- Anemia
More info about NEUROBLASTOMA
Search interest in LMO1
Potential gene panels for LMO1 gene
LMO1 Panel
United States.
By Fulgent Genetics Fulgent Genetics
This panel specifically test the LMO1 gene.
More info about this panel United States.
Hemato-oncology chromosomal microarray Panel
United States.
By Pittsburgh Cytogenetics Laboratory University of Pittsburgh Medical Center Hemato-oncology chromosomal microarray that also includes the following genes: BLM BRAF BRCA1 BRCA2 SMARCB1 KDM5C SMO ABI1 SSX1 SSX2
More info about this panel United States.
NeoTYPE® Discovery Profile for Solid Tumors Panel
United States.
By NeoGenomics Laboratories NeoGenomics Laboratories, Inc. NeoTYPE® Discovery Profile for Solid Tumors that also includes the following genes: BCL6 ROS1 RUNX1 BLM SDHA SDHB SDHC SDHD SF3B1 FOXL2
More info about this panel United States.
Caris MI TumorSeek 592-Gene NGS Panel Panel
United States.
By Caris Life Sciences Caris MI TumorSeek 592-Gene NGS Panel that also includes the following genes: BCL6 BCL7A BCL9 BCR ROS1 RPL10 RPL22 RPL5 RPN1 RUNX1
More info about this panel United States.
Tempus xT assay Panel
United States.
By Tempus Labs, Inc. Tempus xT assay that also includes the following genes: BCL6 RIT1 BCL7A BCR ROS1 RPL5 RPS15 RPS6KB1 RUNX1 RXRA
More info about this panel United States.
Tempus xO assay Panel
United States.
By Tempus Labs, Inc. Tempus xO assay that also includes the following genes: BCL6 RHEB RIPK1 RIPK2 RIPK3 RIT1 BCL7A BCL9 BCR ROBO2
More info about this panel United States.
If you liked this article maybe you will also find interesting the following in-depth articles about other rare diseases, like KCNH1 MMAB MLXIPL STAT2 IRS2 NF1 HLA-C