P2RY11 gene related symptoms and diseases

All the information presented here about the P2RY11 gene and its related diseases, symptoms, and test panels has been aggregated from the following public sources: NCBIGENE,OMIM,ORPHANET,HGNC, Mendelian Rare Disease Search Engine.

Top 5 symptoms and clinical features associated to P2RY11 gene

Symptoms // Phenotype % Cases
Neoplasm Very Common - Between 80% and 100% cases
Brain neoplasm Very Common - Between 80% and 100% cases
Sleep paralysis Very Common - Between 80% and 100% cases
Paroxysmal drowsiness Very Common - Between 80% and 100% cases
Hypnagogic hallucinations Very Common - Between 80% and 100% cases

Other less frequent symptoms and clinical features

Patients with P2RY11 gene alterations may also develop some of the following symptoms and phenotypes:
  • Commonly - More than 50% cases

  • CNS infection
  • Transient global amnesia
  • Abnormal rapid eye movement sleep
  • Narcolepsy
  • Cataplexy
  • Excessive daytime sleepiness
  • Hypersomnia
  • Drowsiness

And 12 more phenotypes, you can get all of them using our tools for rare diseases.


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Rare diseases associated to P2RY11 gene

Here you will find a list of rare diseases related to the P2RY11. You can also use our tool to get a more accurate diagnosis based on your current symptoms.


Alternate names

NARCOLEPSY TYPE 1 Is also known as g√Člineau disease, narcoleptic syndrome 1, narcolepsy-cataplexy


Narcolepsy with cataplexy is a sleep disorder characterized by excessive day-time sleepiness associated with uncontrollable sleep urges and cataplexy (loss of muscle tone often triggered by pleasant emotions).

Most common symptoms of NARCOLEPSY TYPE 1

  • Neoplasm
  • Obesity
  • Hyperactivity
  • Abnormality of the eye
  • Paralysis

More info about NARCOLEPSY TYPE 1


Potential gene panels for P2RY11 gene

P2RY11 Panel

United States.

By Fulgent Genetics Fulgent Genetics

This panel specifically test the P2RY11 gene.

More info about this panel

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