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

SOURCES: OMIM ORPHANET


Potential gene panels for SLC30A8 gene

SLC30A8 Panel

United States.

By Fulgent Genetics Fulgent Genetics

This panel specifically test the SLC30A8 gene.

More info about this panel
United States.

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