ST3GAL4 gene related symptoms and diseases
All the information presented here about the ST3GAL4 gene and its related diseases, symptoms, and test panels has been aggregated from the following public sources: OMIM,NCBIGENE,HGNC, Mendelian Rare Disease Search Engine.
Table of contents:
Top 5 symptoms and clinical features associated to ST3GAL4 gene
| Symptoms // Phenotype | % Cases |
|---|---|
| Intellectual disability | Very Common - Between 80% and 100% cases |
| Intellectual disability, severe | Very Common - Between 80% and 100% cases |
| Syndactyly | Very Common - Between 80% and 100% cases |
| Midface retrusion | Very Common - Between 80% and 100% cases |
| Short foot | Very Common - Between 80% and 100% cases |
Other less frequent symptoms and clinical features
Patients with ST3GAL4 gene alterations may also develop some of the following symptoms and phenotypes:Commonly - More than 50% cases
- Exotropia
- Short toe
- Short chin
- Short 5th finger
- Alternating exotropia
Rare diseases associated to ST3GAL4 gene
Here you will find a list of rare diseases related to the ST3GAL4. You can also use our tool to get a more accurate diagnosis based on your current symptoms.
MENTAL RETARDATION, AUTOSOMAL DOMINANT 4; MRD4
Most common symptoms of MENTAL RETARDATION, AUTOSOMAL DOMINANT 4; MRD4
- Intellectual disability
- Intellectual disability, severe
- Syndactyly
- Midface retrusion
- Short foot
More info about MENTAL RETARDATION, AUTOSOMAL DOMINANT 4; MRD4
Search interest in ST3GAL4
Potential gene panels for ST3GAL4 gene
ST3GAL4 Panel
United States.
By Fulgent Genetics Fulgent Genetics
This panel specifically test the ST3GAL4 gene.
More info about this panel United States.
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