Summary

46 Corticosteroid-binding globulin deficiency is a genetic disorder characterized by extreme tiredness (fatigue), particularly after physical exertion, and low blood pressure (hypotension). corticosteroid-binding globulin (cbg) is a protein primarily produced in the liver that attaches to cortisol, a hormone with numerous functions, including maintaining blood sugar levels, protecting the body from stress, and suppressing inflammation. when cortisol is needed in the body, cbg delivers the cortisol where it is needed and releases it. signs and symptoms of cbg deficiency vary. while some individuals may experience no symptoms, others are found to have a fatty liver and chronic pain. some people with cbg deficiency also have chronic fatigue syndrome. cgb deficiency is caused by mutationsin the serpina6 gene. the serpina6 gene is commonly also referred to as the cbg gene. both autosomal dominantand autosomal recessiveinheritance have been reported. while there is still no cure, treatment options will depend on the type and severity of symptoms present and may involve several specialists

All SNPs

Disease Hierarchy

Disease Interacts with Genes

Disease Interacts with Substances

Processes Associated With Trait

Symptoms Associated With Trait