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  2. Rare Disease Genes
  3. FARP2

FARP2 gene related symptoms and diseases

All the information presented here about the FARP2 gene and its related diseases, symptoms, and test panels has been aggregated from the following public sources: OMIM,HGNC,NCBIGENE, Mendelian Rare Disease Search Engine.

Table of contents:

Top 5 symptoms and clinical features associated to FARP2 gene

Symptoms // Phenotype % Cases
Intellectual disability Very Common - Between 80% and 100% cases
Broad nasal tip Very Common - Between 80% and 100% cases
Broad-based gait Very Common - Between 80% and 100% cases
Sparse scalp hair Very Common - Between 80% and 100% cases
Congenital diaphragmatic hernia Very Common - Between 80% and 100% cases

Other less frequent symptoms and clinical features

Patients with FARP2 gene alterations may also develop some of the following symptoms and phenotypes:

  • Commonly - More than 50% cases

  • Narrow forehead
  • Eczema
  • Wide intermamillary distance
  • Underdeveloped nasal alae
  • Short metacarpal
  • Round face
  • Sleep disturbance
  • Short phalanx of finger

And 88 more phenotypes, you can get all of them using our tools for rare diseases.

Rare diseases associated to FARP2 gene

Here you will find a list of rare diseases related to the FARP2. You can also use our tool to get a more accurate diagnosis based on your current symptoms.


2Q37 MICRODELETION SYNDROME

Alternate names

2Q37 MICRODELETION SYNDROME Is also known as albright hereditary osteodystrophy-like syndrome, del(2)(q37), monosomy 2q37-qter, brachydactyly-intellectual disability syndrome, albright hereditary osteodystrophy type 3, brachydactyly-mental retardation syndrome, bdmr, deletion 2q37-qter, deletion 2q37

Description

Deletion 2q37 or monosomy 2q37 is a chromosomal anomaly involving deletion of chromosome band 2q37 and manifests as three major clinical findings: developmental delay, skeletal malformations and facial dysmorphism.

Most common symptoms of 2Q37 MICRODELETION SYNDROME

  • Intellectual disability
  • Seizures
  • Global developmental delay
  • Short stature
  • Generalized hypotonia


More info about 2Q37 MICRODELETION SYNDROME

SOURCES: ORPHANET MESH OMIM


Potential gene panels for FARP2 gene

FARP2 Panel

United States.

By Fulgent Genetics Fulgent Genetics

This panel specifically test the FARP2 gene.

More info about this panel
United States.

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