Directory
Glucose-6-phosphate translocase deficiency
Glucose-6-phosphate translocase deficiency, also known as Fabry disease, is a rare inherited disorder caused by...
Glucose-6-phosphate dehydrogenase deficiency
Glucose-6-phosphate dehydrogenase (G6PD) deficiency is an inherited disorder that occurs when an enzyme that plays a role in the body's metabolism is malfunctioning.
Glucose phosphate isomerase deficiency
Glucose phosphate isomerase deficiency (GPI) is a rare, inherited disorder of carbohydrate metabolism that results in...
Growth Hormone Deficiency (GHD)
Growth hormone deficiency (GHD) is an endocrine disorder characterized by insufficient production of growth hormone (GH), which plays a role in...
Guanidinoacetate methyltransferase deficiency
Guanidinoacetate methyltransferase (GAMT) deficiency is a rare, inherited metabolic disorder that results in...
Glucose-galactose malabsorption deficiency
Glucose-galactose malabsorption deficiency is a rare, inherited disorder characterized by impaired absorption of glucose and...
Glucose transporter deficiency
Glucose transport deficiency (GTI) is a rare inherited disorder that involves abnormal metabolism of the...
Greenberg's dysplasia
Greenberg's Dysplasia is a rare inherited disorder characterized by abnormalities in the development of...
Gastrointestinal bleeding
Gastrointestinal bleeding (GIB) is a pathological condition characterized by loss of blood from any part of the stomach...
Gastrointestinal fistula
A gastrointestinal fistula is an abnormal communication between different parts of the intestine or between the intestine and other ...
Gallbladder disease
Gallbladder disease is a group of disorders associated with the functional state and structure of this organ, the response...
Giardia infection
Giardia infection, caused by the protozoan Giardia lamblia, is one of the most common infectious diseases...
Gallstones
Gallstones, also known as cholelithiasis, are hard lumps that form in the gallbladder from stagnant...
Guttate psoriasis
Guttate psoriasis, also known as psoriasis vulgaris or type III, is a form of chronic inflammatory psoriasis that occurs in the...
Ganglion cyst
A ganglion cyst is a benign, fluid-filled sac that forms in the joint area.
Granuloma annulare
Granuloma annulare is a chronic inflammatory disorder characterized by the formation of painless, reddish-brown...
Gastric lymphoma
Gastric lymphoma is a malignant neoplasm arising from the lymphoid tissue of the gastric wall. It is rare, but with...
Gastric motility disorder
Gastric motility disorder is a complex syndrome characterized by a decrease or change in the motor activity of the stomach...
Glossopharyngeal neuralgia
Glossopharyngeal neuralgia is a syndrome characterized by acute, paroxysmal pain in the area or perioral...
Tumor of the eardrum
A tumor of the eardrum is an abnormal growth of tissue located in the area of the eardrum, which can...
Germ cell tumor
Germ cell tumors (hemigendromas) are a group of rare tumors that originate from immature germ cells. These are...
Tumor of the jugular glomus
A jugular glomus tumor (glomus tumor) is a rare, benign tumor that arises from specialized cells that...
Osteodysplastic geroderma
Osteodysplastic geroderma is a rare genetic disorder characterized by abnormal structure and function of the connective tissue...
Perforation of the gastrointestinal tract
Gastrointestinal (GI) perforation is a serious medical condition characterized by the formation of a hole in the gastrointestinal tract...
Gastroesophageal junction cancer
Gastroesophageal junction cancer (GEJC) is a malignant neoplasm that occurs at the junction of the esophagus and stomach.
Gallbladder cancer
Gallbladder cancer is a malignant neoplasm that arises from the epithelial cells of the gallbladder mucosa. This...
Graft-versus-host disease (GVHD)
Graft-versus-host disease (GVHD) is a serious complication that can occur following allogeneic transplantation of...
GAPO syndrome
Hypoplasia of the Adeno-Parathyroid Sensory Glands (HAPS) syndrome is a rare genetic disorder characterized by a lack of...
HEMS syndrome
HEMSS (hemihyperesthesia with myelopathy and spinal stenosis) syndrome is a rare neurological disorder characterized by...
Gardner's syndrome
Gardner syndrome (GS) is a genetic disorder that belongs to the group of hereditary polyposis syndromes. It is characterized by...
