1. Mendelian
  2. Rare Disease Genes
  3. FMR3

FMR3 gene related symptoms and diseases

All the information presented here about the FMR3 gene and its related diseases, symptoms, and test panels has been aggregated from the following public sources: HGNC,ORPHANET,NCBIGENE, Mendelian Rare Disease Search Engine.

Table of contents:

Top 5 symptoms and clinical features associated to FMR3 gene

Symptoms // Phenotype % Cases
Intellectual disability Very Common - Between 80% and 100% cases
Aggressive behavior Very Common - Between 80% and 100% cases
Agitation Very Common - Between 80% and 100% cases
Obsessive-compulsive behavior Very Common - Between 80% and 100% cases
Impulsivity Very Common - Between 80% and 100% cases

Other less frequent symptoms and clinical features

Patients with FMR3 gene alterations may also develop some of the following symptoms and phenotypes:

  • Commonly - More than 50% cases

  • Prominent nasal bridge
  • Attention deficit hyperactivity disorder
  • Autistic behavior
  • Intellectual disability, moderate
  • Hyperactivity
  • Global developmental delay
  • Abnormality of metabolism/homeostasis
  • Intellectual disability, mild

And 6 more phenotypes, you can get all of them using our tools for rare diseases.

Rare diseases associated to FMR3 gene

Here you will find a list of rare diseases related to the FMR3. You can also use our tool to get a more accurate diagnosis based on your current symptoms.


FRAXE INTELLECTUAL DISABILITY

Alternate names

FRAXE INTELLECTUAL DISABILITY Is also known as fraxe mental retardation syndrome, intellectual disability associated with fragile site fraxe

Description

FRAXE is a form of nonsyndromic X-linked mental retardation (NS-XLMR) characterized by mild intellectual deficit. FRAXE is the most common form of NS-XLMR.

Most common symptoms of FRAXE INTELLECTUAL DISABILITY

  • Intellectual disability
  • Global developmental delay
  • Short stature
  • Microcephaly
  • Delayed speech and language development


More info about FRAXE INTELLECTUAL DISABILITY

SOURCES: ORPHANET OMIM



If you liked this article maybe you will also find interesting the following in-depth articles about other rare diseases, like ABCD4 BBS4 IGKC KCNQ1OT1 EXT2 ABCG2