Directory
Follicular lymphoma
Follicular lymphoma (FL) is one of the most common forms of non-Hodgkin's lymphoma, which is characterized by slow...
Follicular ichthyosis
Follicular ichthyosis, also known as ichthyosis, is a group of inherited skin disorders characterized by abnormal...
Follicular thyroid cancer
Follicular thyroid cancer (FTCC) is a malignant tumor that originates from the cells of the thyroid follicles...
Friedrich Ataxia
Friedrich ataxia is an inherited neurodegenerative disorder characterized by progressive loss of motor coordination...
Frontometaphyseal dysplasia
Frontometaphyseal dysplasia is a rare genetic disorder characterized by skeletal developmental abnormalities, characteristic changes...
Frontonasal dysplasia, Klippel-Feil syndrome
Frontonasal dysplasia and Klippel-Feil syndrome are conditions characterized by developmental abnormalities of the craniofacial ...
Fucosidosis
Fucosidosis is a rare genetic disorder belonging to the group of lysosomal storage diseases associated with the absence or reduction of...
Frequent or urgent urination
Urinary frequency or urgency is a condition characterized by increased frequency of urination, which is accompanied by either...
Ectodermal dysplasia of the face
Facial ectodermal dysplasia is a group of congenital syndromes characterized by abnormalities in tissue development, pro...
Ulcers of the female genital organs
Female genital ulcers are deep lesions of the tissues of the external and internal genital organs in women that can...
Adenocarcinoma of the gallbladder
Gallbladder adenocarcinoma is a malignant neoplasm that arises from the cells of the glandular epithelium lining the...
Allergy to grass
Grass allergy, or hay fever, is one of the types of allergic reactions that occur when interacting with allergens, ...
Aldosteronism responsive to glucocorticoid treatment
Aldosteronism is an endocrine disorder caused by hypersecretion of aldosterone, a mineralocorticoid hormone produced...
Goldenhar's disease
Goldenhar disease, also known as oral-oculo-vertebral dysplasia syndrome, is a rare genetic disorder...
Gorham's disease
Gorham's disease (or "Gorham's syndrome") is a rare and complex disorder characterized by the progressive destruction of ...
Gaucher disease
Gaucher disease is an inherited metabolic disorder that involves abnormal lipid metabolism. This disease is caused by...
Gaucher disease type 1
Gaucher disease type 1 (BG-1) is a genetic disorder characterized by a deficiency of the enzyme glucocerebrosidase,...
Gaucher disease type 2
Gaucher disease type 2 (BG2) is a rare inherited disorder that belongs to the group of lysosomal storage diseases caused by de...
Gaucher disease type 3
Gaucher disease type 3, or the neurogenerative form of the disease, is a rare inherited disorder associated with a defective...
Graves' disease
Graves' disease (or toxic goiter, diffuse toxic goiter) is an autoimmune disease characterized by hyperf...
Grover's disease
Grover's disease, also known as acanthosis gravidarum, is a rare skin disorder characterized by episodic flare-ups of...
Glycogen storage disease type 5
Glycogen storage disease type 5 (Glycogen storage disease 5) is a rare inherited metabolic disorder associated with the accumulation of g...
Glycogen storage disease type 0
Glycogen storage disease type 0 is a rare, inherited metabolic disorder caused by a deficiency of enzymes...
Glycogen storage disease type 13
Glycogen storage disease type 13 (GSD-13) is a rare inherited disorder characterized by a metabolic disorder...
Glycogen storage disease type 3
Glycogen storage disease type 3 (Cori disease) is a genetic disorder characterized by a deficiency of the enzyme glycogen...
Glycogen storage disease type 6
Glycogen storage disease type 6, also known as Eppler disease or glycogen storage disease type 6, is a rare inherited...
Glycogen storage disease type 7
Glycogen storage disease type 7, also known as phospholirosine glycogen storage disease, is a rare inherited disorder related to...
Glycogen storage disease type 9
Glycogen storage disease type 9 is a rare metabolic disorder that involves defective glycogen metabolism in the...
Rotational atrophy of the choroid and retina
Rotational choroidal-retinal atrophy (ROCRA) is a rare, progressive degenerative disorder characterized by...
Galactosemia
Galactosemia is a hereditary metabolic disease associated with a violation of the metabolism of galactose, sucrose and lactose in the body. ...
