OGT gene related symptoms and diseases

All the information presented here about the OGT gene and its related diseases, symptoms, and test panels has been aggregated from the following public sources: HGNC,OMIM,NCBIGENE, Mendelian Rare Disease Search Engine.

Top 5 symptoms and clinical features associated to OGT gene

Symptoms // Phenotype % Cases
Intellectual disability Very Common - Between 80% and 100% cases
Wide nose Very Common - Between 80% and 100% cases
Slender finger Very Common - Between 80% and 100% cases
High hypermetropia Very Common - Between 80% and 100% cases
Supernumerary nipple Very Common - Between 80% and 100% cases

Other less frequent symptoms and clinical features

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

  • Spastic diplegia
  • Drooling
  • Bicuspid aortic valve
  • Finger clinodactyly
  • Amblyopia
  • Open mouth
  • Narrow forehead
  • Decreased testicular size

And 16 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 OGT gene

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


MENTAL RETARDATION, X-LINKED 106; MRX106


Most common symptoms of MENTAL RETARDATION, X-LINKED 106; MRX106

  • Intellectual disability
  • Global developmental delay
  • Generalized hypotonia
  • Microcephaly
  • Hypertelorism


More info about MENTAL RETARDATION, X-LINKED 106; MRX106

SOURCES: OMIM


Potential gene panels for OGT gene

NGS XLID Panel Panel

United States.

By Greenwood Genetic Center Diagnostic Laboratories Greenwood Genetic Center NGS XLID Panel that also includes the following genes: RPL10 RPS6KA3 SLC16A2 SLC9A6 SMC1A KDM5C SMS SOX3 CDKL5 SYN1

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 NR1I2 ZNF711 ANK1 KCNT1 CLCN1 CYP3A4

Need help with a diagnosis?

Learn more about how to achieve it with Mendelian


Learn more