HAGH gene related symptoms and diseases

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

Top 5 symptoms and clinical features associated to HAGH gene

Symptoms // Phenotype % Cases
Elliptocytosis Very Common - Between 80% and 100% cases
Glyoxalase deficiency Very Common - Between 80% and 100% cases

Rare diseases associated to HAGH gene

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


HYDROXYACYL GLUTATHIONE HYDROLASE DEFICIENCY


Alternate names

HYDROXYACYL GLUTATHIONE HYDROLASE DEFICIENCY Is also known as glyoxalase ii deficiency

Most common symptoms of HYDROXYACYL GLUTATHIONE HYDROLASE DEFICIENCY

  • Elliptocytosis
  • Glyoxalase deficiency


More info about HYDROXYACYL GLUTATHIONE HYDROLASE DEFICIENCY

SOURCES: OMIM MESH


Potential gene panels for HAGH gene

MitoMet®Plus aCGH Analysis Panel

United States.

By Baylor Miraca Genetics Laboratories MitoMet®Plus aCGH Analysis that also includes the following genes: RGS9 RHO GRK1 RLBP1 RNASEL BCS1L RP1 RP2 RP9 RPE65

More info about this panel

HAGH Panel

United States.

By Fulgent Genetics Fulgent Genetics

This panel specifically test the HAGH gene.

More info about this panel


If you liked this article maybe you will also find interesting the following in-depth articles about other rare diseases, like BMP15 GCKR

Need help with a diagnosis?

Learn more about how to achieve it with Mendelian


Learn more