Directory
Giant cell myocarditis
Giant cell myocarditis is a rare but serious inflammatory disease of the heart characterized by the proliferation of giant cell...
Giant axonal neuropathy
Giant axonal neuropathy (GAN) is a rare inherited disorder characterized by axonal degeneration and demyelination.
Giant hamartoma of the mammary gland
Giant hamartoma of the breast is a rare benign tumor characterized by proliferation of various types of tissue...
Giant congenital melanocytic nevus
Giant congenital melanocytic nevus (GCMN) is a developmental abnormality of melanocytes characterized by the formation of large...
Giant congenital nevus
Giant congenital nevus (GCN) is a skin lesion that results from hyperplasia of melanocytes, often...
Giant papillary conjunctivitis
Giant papillary conjunctivitis (GPC) is a chronic inflammatory disease of the conjunctiva characterized by the formation of large...
Gingivostomatitis
Gingivostomatitis is an inflammatory disease of the oral cavity that affects both the gums and the mucous membrane. Clinically, it is p...
Glaucoma
Glaucoma is a group of progressive diseases characterized by increased intraocular pressure, which can lead to...
Glioblastoma
Glioblastoma is a malignant tumor arising from glial cells of the central nervous system, characterized by aggressive ...
Glioma
Gliomas are malignant tumors that arise from glial cells, which support and protect neurons in the central nervous system.
Gliomatosis cerebri
Gliomatosis cerebri is a rare and serious disease associated with the formation of multiple gliomas, which are...
Gliosarcoma
Gliosarcoma is a rare malignant tumor originating from glial cells in the brain. It is a combination of...
Glycine encephalopathy
Glycine encephalopathy (GE) is a rare inherited disorder that belongs to a group of metabolic disorders initiated by abnormal...
Glomerulonephritis
Glomerulonephritis is a kidney disease characterized by inflammation of the glomeruli (small filtering units) in the kidneys. It can occur...
Glossitis
Glossitis is an inflammatory disease of the tongue, characterized by changes in its structure and surface, which can manifest itself in the form of...
Glossodynia
Glossodynia is a complex and often poorly understood condition characterized by persistent or intermittent pain, discomfort, or...
Glutaric acidemia type 1
Glutaric acidemia type 1 (GA1) is a rare inherited metabolic disorder caused by a deficiency of the enzyme glutaryl-C...
Glutaric acidemia type 2
Glutaric acidemia type 2 (GA-2) is a rare inherited metabolic disorder caused by a deficiency of a specific...
Glucagonoma
Glucagonoma is a rare endocrine tumor process characterized by hypersecretion of glucagon, which leads to the development of r...
Gonococcal arthritis
Gonococcal arthritis, also known as gonorrheal arthritis, is an infectious disease caused by the bacterium Neisseria gonorrhoea...
Gonococcal conjunctivitis
Gonococcal conjunctivitis is an acute infectious disease of the eye caused by the bacterium Neisseria gonorrhoeae, best known as...
Wegener's granulomatosis
Wegener's granulomatosis (WG) is a rare but serious autoimmune disease characterized by systemic inflammation, p...
Granulomatous hypophysitis
Granulomatous hypophysitis (GH) is a rare inflammatory disorder characterized by the formation of granulomas in the...
Gumma
Gumma is a specific pathological process, the essence of which lies in the formation of gummatous lesions, characterized by not...
GABA transaminase deficiency
GABA transaminase (GABA-T) deficiency is a rare genetic disorder that results in abnormal gamma-aminobutyric acid metabolism...
GTP cyclohydrolase 1 deficiency
GTP cyclohydrolase 1 (GCH1) deficiency is a rare inherited disorder associated with a disorder of neurotransmitter metabolism that...
Galactose epimerase deficiency
Galactose epimerase deficiency is a rare genetic disorder that belongs to a group of inherited disorders of carbohydrate metabolism. E...
Galactokinase deficiency
Galactokinase deficiency is a rare inherited disorder caused by a deficiency of the enzyme galactokinase, which is responsible for...
Glyceraldehyde-3-phosphate dehydrogenase deficiency
Glyceraldehyde-3-phosphate dehydrogenase (GAPDH) deficiency is a rare inherited disorder that belongs to a group of metabolic disorders called glyceraldehyde-3-phosphate dehydrogenase (GAPDH).
Glutamate decarboxylase deficiency
Glutamate decarboxylase (GDC) deficiency is a neurological disorder associated with a deficiency of the enzyme glutamate decarboxylase...
