FBXO11 gene related symptoms and diseases
All the information presented here about the FBXO11 gene and its related diseases, symptoms, and test panels has been aggregated from the following public sources: HGNC,NCBIGENE,OMIM, Mendelian Rare Disease Search Engine.
Top 5 symptoms and clinical features associated to FBXO11 gene
Symptoms // Phenotype | % Cases |
---|---|
Intellectual disability | Very Common - Between 80% and 100% cases |
Short foot | Very Common - Between 80% and 100% cases |
Deeply set eye | Very Common - Between 80% and 100% cases |
Microtia | Very Common - Between 80% and 100% cases |
Hypermetropia | Very Common - Between 80% and 100% cases |
Other less frequent symptoms and clinical features
Patients with FBXO11 gene alterations may also develop some of the following symptoms and phenotypes:Commonly - More than 50% cases
- Long face
- Downturned corners of mouth
- Thick vermilion border
- Small hand
- Everted lower lip vermilion
- Tapered finger
- High forehead
- Epileptic encephalopathy
And 31 more phenotypes, you can get all of them using our tools for rare diseases.
Rare diseases associated to FBXO11 gene
Here you will find a list of rare diseases related to the FBXO11. You can also use our tool to get a more accurate diagnosis based on your current symptoms.
INTELLECTUAL DEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES AND BEHAVIORAL ABNORMALITIES; IDDFBA
Most common symptoms of INTELLECTUAL DEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES AND BEHAVIORAL ABNORMALITIES; IDDFBA
- Intellectual disability
- Seizures
- Global developmental delay
- Short stature
- Generalized hypotonia
More info about INTELLECTUAL DEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES AND BEHAVIORAL ABNORMALITIES; IDDFBA
SOURCES: OMIM
Search interest in FBXO11
Potential gene panels for FBXO11 gene
FBXO11 Panel
By Fulgent Genetics Fulgent Genetics
This panel specifically test the FBXO11 gene.
More info about this panelFoundationOne® Heme Panel
By Foundation Medicine, Inc. FoundationOne® Heme that also includes the following genes: BCL6 BCL7A ROS1 RUNX1 BLM SDHA SDHB SDHC SDHD SF3B1
More info about this panelCaris MI TumorSeek 592-Gene NGS Panel Panel
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 panelProvidence Personalized Medicine Panel - Solid Tumor Panel
By Providence Regional Laboratories Providence Health and Services Providence Personalized Medicine Panel - Solid Tumor that also includes the following genes: BCR ROS1 RUNX1 SDHA SDHB SDHC SDHD SF3B1 SRSF2 FOXL2
More info about this panelTempus xT assay Panel
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 panelTempus xO assay Panel
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 panelIf you liked this article maybe you will also find interesting the following in-depth articles about other rare diseases, like BMPR1B ABCD4 SALL2 SLC20A2 RPS17