1. Mendelian
  2. Rare Disease Genes
  3. DLG3-AS1

DLG3-AS1 gene related symptoms and diseases

All the information presented here about the DLG3-AS1 gene and its related diseases, symptoms, and test panels has been aggregated from the following public sources: HGNC,NCBIGENE, Mendelian Rare Disease Search Engine.

Table of contents:

Top 5 symptoms and clinical features associated to DLG3-AS1 gene

Symptoms // Phenotype % Cases
Intellectual disability Very Common - Between 80% and 100% cases
Seizures Very Common - Between 80% and 100% cases
Global developmental delay Very Common - Between 80% and 100% cases
Generalized hypotonia Very Common - Between 80% and 100% cases
Strabismus Very Common - Between 80% and 100% cases

Other less frequent symptoms and clinical features

Patients with DLG3-AS1 gene alterations may also develop some of the following symptoms and phenotypes:

  • Commonly - More than 50% cases

  • High palate
  • Delayed speech and language development
  • Intellectual disability, severe
  • Behavioral abnormality
  • Upslanted palpebral fissure
  • Narrow chest
  • Enuresis

Rare diseases associated to DLG3-AS1 gene

Here you will find a list of rare diseases related to the DLG3-AS1. You can also use our tool to get a more accurate diagnosis based on your current symptoms.


MENTAL RETARDATION, X-LINKED 90; MRX90

Most common symptoms of MENTAL RETARDATION, X-LINKED 90; MRX90

  • Intellectual disability
  • Seizures
  • Global developmental delay
  • Generalized hypotonia
  • Strabismus


More info about MENTAL RETARDATION, X-LINKED 90; MRX90

SOURCES: OMIM



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