Glucocorticoid-induced osteoporosis is a condition in which prolonged use of glucocorticoid medications leads to weakened bones and an increased risk...

Glucocorticoid-remediable aldosteronism, also known as familial hyperaldosteronism type I, is a heritable form of primary aldosteronism that primarily...

Glucocorticoid resistance is an endocrine condition characterized by an impaired response to cortisol despite elevated hormone levels. It is caused by...

Glucose-galactose malabsorption (GGM), also known as SGLT1 deficiency, is a very rare genetic metabolic disorder affecting the gastrointestinal system...

Glucose intolerance is a condition characterized by the inability to properly regulate blood glucose levels, resulting in episodes of elevated blood s...

Glucose transport disorder is an inherited metabolic condition that arises from disruptions in the cellular transport of glucose. Genetic studies have...

GLUT1 deficiency syndrome is a condition that affects the brain, known to cause seizures and other neurological issues. It occurs because of impaired...

Glutamate pyruvate transaminase 2 deficiency, also known as GPT2 deficiency, is an ultra-rare neurodevelopmental disorder that primarily affects brain...

Glutaminase deficiency is a condition that primarily affects the brain and respiratory systems. It is caused by mutations in the GLS gene, which disru...

Glutaric acidemia type 3 is a peroxisomal metabolic disorder caused by deficient activity of the enzyme glutaryl-CoA oxidase, which is encoded by the...

Glutaryl-CoA dehydrogenase deficiency is an autosomal recessive neurometabolic disorder that primarily affects the brain, with characteristic episodes...

Glutathione synthetase deficiency with 5-oxoprolinuria is an inherited metabolic disorder that affects the body’s ability to produce the antioxidant g...

Glutathione synthetase deficiency without 5-oxoprolinuria is an inherited metabolic condition that primarily affects the red blood cells and other tis...