NAA15 gene related symptoms and diseases

All the information presented here about the NAA15 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.

Top 5 symptoms and clinical features associated to NAA15 gene

Symptoms // Phenotype % Cases
Intellectual disability Very Common - Between 80% and 100% cases
Atrial septal defect Very Common - Between 80% and 100% cases
Mutism Very Common - Between 80% and 100% cases
Autistic behavior Very Common - Between 80% and 100% cases
Aggressive behavior Very Common - Between 80% and 100% cases

Other less frequent symptoms and clinical features

Patients with NAA15 gene alterations may also develop some of the following symptoms and phenotypes:
  • Commonly - More than 50% cases

  • Autism
  • Hyperactivity
  • Abnormal heart morphology
  • Motor delay
  • Seizures
  • Delayed speech and language development
  • Feeding difficulties
  • Abnormal facial shape

And 5 more phenotypes, you can get all of them using our tools for rare diseases.

Mendelian

Accelerate your rare disease diagnosis with us

Learn more

Rare diseases associated to NAA15 gene

Here you will find a list of rare diseases related to the NAA15. You can also use our tool to get a more accurate diagnosis based on your current symptoms.


MENTAL RETARDATION, AUTOSOMAL DOMINANT 50; MRD50


Most common symptoms of MENTAL RETARDATION, AUTOSOMAL DOMINANT 50; MRD50

  • Intellectual disability
  • Seizures
  • Global developmental delay
  • Short stature
  • Generalized hypotonia


More info about MENTAL RETARDATION, AUTOSOMAL DOMINANT 50; MRD50

SOURCES: OMIM


Potential gene panels for NAA15 gene

Autism Spectrum Disorders Sequencing Panel with CNV Detection Panel

United States.

By PreventionGenetics PreventionGenetics Autism Spectrum Disorders Sequencing Panel with CNV Detection that also includes the following genes: SCN1A SCN2A SGSH BRAF SLC6A1 SLC9A6 SPAST CDKL5 STXBP1 SYN2

More info about this panel

Congenital Heart Defects Panel Panel

Germany.

By CeGaT GmbH Congenital Heart Defects Panel that also includes the following genes: SEMA3E TBX1 TBX20 TBX3 TBX5 TFAP2B TLL1 ZIC3 ACTC1 CRELD1

More info about this panel

NAA15 Panel

United States.

By Fulgent Genetics Fulgent Genetics

This panel specifically test the NAA15 gene.

More info about this panel

Congenital Structural Heart Disease Panel Panel

Finland.

By Blueprint Genetics Congenital Structural Heart Disease Panel that also includes the following genes: BMPR2 SOS2 TBX1 TBX20 TBX5 TFAP2B TLL1 ZIC3 ACTA2 ACTB

More info about this panel


If you liked this article maybe you will also find interesting the following in-depth articles about other rare diseases, like NTF3

Need help with a diagnosis?

Learn more about how to achieve it with Mendelian


Learn more