NTN1 gene related symptoms and diseases
All the information presented here about the NTN1 gene and its related diseases, symptoms, and test panels has been aggregated from the following public sources: HGNC,ORPHANET,NCBIGENE,OMIM, Mendelian Rare Disease Search Engine.
Top 5 symptoms and clinical features associated to NTN1 gene
| Symptoms // Phenotype | % Cases |
|---|---|
| Pain | Very Common - Between 80% and 100% cases |
| Intellectual disability, mild | Very Common - Between 80% and 100% cases |
| Agenesis of corpus callosum | Very Common - Between 80% and 100% cases |
| Myalgia | Very Common - Between 80% and 100% cases |
| Abnormality of movement | Very Common - Between 80% and 100% cases |
Other less frequent symptoms and clinical features
Patients with NTN1 gene alterations may also develop some of the following symptoms and phenotypes:Commonly - More than 50% cases
- Specific learning disability
- Clumsiness
- Situs inversus totalis
- Hypogonadotrophic hypogonadism
- Cerebral palsy
- Easy fatigability
- Fused cervical vertebrae
- Poor fine motor coordination
And 3 more phenotypes, you can get all of them using our tools for rare diseases.
Rare diseases associated to NTN1 gene
Here you will find a list of rare diseases related to the NTN1. You can also use our tool to get a more accurate diagnosis based on your current symptoms.
FAMILIAL CONGENITAL MIRROR MOVEMENTS
Alternate names
FAMILIAL CONGENITAL MIRROR MOVEMENTS Is also known as hereditary congenital controlateral synkinesia, isolated congenital controlateral synkinesia, hereditary congenital mirror movements, isolated congenital mirror movements, familial congenital controlateral synkinesia
Most common symptoms of FAMILIAL CONGENITAL MIRROR MOVEMENTS
- Pain
- Intellectual disability, mild
- Agenesis of corpus callosum
- Myalgia
- Abnormality of movement
More info about FAMILIAL CONGENITAL MIRROR MOVEMENTS
Search interest in NTN1
Potential gene panels for NTN1 gene
NTN1 Panel
United States.
By Fulgent Genetics Fulgent Genetics
This panel specifically test the NTN1 gene.
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 DLX5 AICDA NUP155 TUBB3 ACSF3 AKR1C1 MYBPC1