1. Mendelian
  2. Rare Disease Genes
  3. GPR88

GPR88 gene related symptoms and diseases

All the information presented here about the GPR88 gene and its related diseases, symptoms, and test panels has been aggregated from the following public sources: NCBIGENE,HGNC,OMIM, Mendelian Rare Disease Search Engine.

Table of contents:

Top 5 symptoms and clinical features associated to GPR88 gene

Symptoms // Phenotype % Cases
Intellectual disability Very Common - Between 80% and 100% cases
Global developmental delay Very Common - Between 80% and 100% cases
Poor speech Very Common - Between 80% and 100% cases
Chorea Very Common - Between 80% and 100% cases
Involuntary movements Very Common - Between 80% and 100% cases

Other less frequent symptoms and clinical features

Patients with GPR88 gene alterations may also develop some of the following symptoms and phenotypes:

  • Commonly - More than 50% cases

  • Dyscalculia
  • Abnormal head movements

Rare diseases associated to GPR88 gene

Here you will find a list of rare diseases related to the GPR88. You can also use our tool to get a more accurate diagnosis based on your current symptoms.


CHOREA, CHILDHOOD-ONSET, WITH PSYCHOMOTOR RETARDATION; COCPMR

Most common symptoms of CHOREA, CHILDHOOD-ONSET, WITH PSYCHOMOTOR RETARDATION; COCPMR

  • Intellectual disability
  • Global developmental delay
  • Poor speech
  • Chorea
  • Involuntary movements


More info about CHOREA, CHILDHOOD-ONSET, WITH PSYCHOMOTOR RETARDATION; COCPMR

SOURCES: OMIM



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