HLX-AS1 gene related symptoms and diseases

All the information presented here about the HLX-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.

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

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

Search interest in HLX-AS1

If you liked this article maybe you will also find interesting the following in-depth articles about other rare diseases, like DSG2-AS1