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
Search interest in HAGH
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 United States.
HAGH Panel
United States.
By Fulgent Genetics Fulgent Genetics
This panel specifically test the HAGH gene.
More info about this panel United States.
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