SLC30A8 gene related symptoms and diseases
All the information presented here about the SLC30A8 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.
Top 5 symptoms and clinical features associated to SLC30A8 gene
Symptoms // Phenotype | % Cases |
---|---|
Diabetes mellitus | Very Common - Between 80% and 100% cases |
Type II diabetes mellitus | Very Common - Between 80% and 100% cases |
Insulin resistance | Very Common - Between 80% and 100% cases |
Type I diabetes mellitus | Very Common - Between 80% and 100% cases |
Hyperinsulinemia | Very Common - Between 80% and 100% cases |
Other less frequent symptoms and clinical features
Patients with SLC30A8 gene alterations may also develop some of the following symptoms and phenotypes:Commonly - More than 50% cases
- Hyperglycemia
- Glucose intolerance
- Fasting hyperinsulinemia
- Decreased waist to hip ratio
Rare diseases associated to SLC30A8 gene
Here you will find a list of rare diseases related to the SLC30A8. You can also use our tool to get a more accurate diagnosis based on your current symptoms.
DIABETES MELLITUS, NONINSULIN-DEPENDENT; NIDDM
Alternate names
DIABETES MELLITUS, NONINSULIN-DEPENDENT; NIDDM Is also known as noninsulin-dependent diabetes mellitus, maturity-onset diabetes, diabetes mellitus, type ii, t2d
Most common symptoms of DIABETES MELLITUS, NONINSULIN-DEPENDENT; NIDDM
- Diabetes mellitus
- Type II diabetes mellitus
- Insulin resistance
- Type I diabetes mellitus
- Hyperinsulinemia
More info about DIABETES MELLITUS, NONINSULIN-DEPENDENT; NIDDM
Search interest in SLC30A8
Potential gene panels for SLC30A8 gene
SLC30A8 Panel
By Fulgent Genetics Fulgent Genetics
This panel specifically test the SLC30A8 gene.
More info about this panelIf you liked this article maybe you will also find interesting the following in-depth articles about other rare diseases, like PRPH EBF3 CALM2 UVSSA HCN1 ACP2 KRT71