PLEKHG1 gene related symptoms and diseases

All the information presented here about the PLEKHG1 gene and its related diseases, symptoms, and test panels has been aggregated from the following public sources: HGNC,NCBIGENE, Mendelian Rare Disease Search Engine.

Top 5 symptoms and clinical features associated to PLEKHG1 gene

Symptoms // Phenotype	% Cases
Intellectual disability	Very Common - Between 80% and 100% cases
Increased mean corpuscular volume	Very Common - Between 80% and 100% cases
Leukocytosis	Very Common - Between 80% and 100% cases
Osteomyelitis	Very Common - Between 80% and 100% cases
Microcytic anemia	Very Common - Between 80% and 100% cases

Other less frequent symptoms and clinical features

Patients with PLEKHG1 gene alterations may also develop some of the following symptoms and phenotypes:

• Commonly - More than 50% cases

• Myeloid leukemia
• Wheezing
• Iron deficiency anemia
• Poor appetite
• Aseptic necrosis
• Reticulocytosis
• Thrombocytosis
• Abnormality of the vasculature

And 57 more phenotypes, you can get all of them using our tools for rare diseases.

Rare diseases associated to PLEKHG1 gene

Here you will find a list of rare diseases related to the PLEKHG1. You can also use our tool to get a more accurate diagnosis based on your current symptoms.

Search interest in PLEKHG1

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