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.

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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

SOURCES: ORPHANET OMIM


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


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