18
Apr
Lichen sclerosus
Lichen sclerosus (lichen sclerosus) is a chronic inflammatory skin disease characterized by impaired...
Directory
18
Apr
Nodules in the lungs
Lung nodules, also known as pulmonary nodules, are localized growths in the lung tissue that may be...
18
Apr
Lump in the abdomen
A lump in the abdomen is a clinical manifestation that may indicate various pathologies, including tumors,...
18
Apr
leukodystrophy
Leukodystrophy is a group of hereditary diseases associated with impaired myelination of nerve fibers. These diseases...
18
Apr
leukoplakia
Leukoplakia is a chronic disease characterized by excessive growth of squamous epithelium of the mucous membrane, most often the oral cavity...
18
Apr
leukocytosis
Leukocytosis is a condition characterized by an increase in the level of leukocytes (white blood cells) in the blood. This phenomenon usually occurs with...
18
Apr
listeriosis
Listeriosis is an infectious disease caused by the bacterium Listeria monocytogenes. This gram-negative bacterium belongs to the family...
18
Apr
MPI-CDG
MPI-CDG (angiopathy), also known as MPI-civil disgroupation, is a rare genetic disorder related to...
18
Apr
Mittelschmerz
Mittelschmerz, or mid-term pain, is a phenomenon that occurs in women during ovulation, when the egg is released...
18
Apr
Meige's disease
Meige's disease, or osteomalaxia, is characterized by a metabolic disorder in bone tissue, which leads to its softening and increased...
18
Apr
Antenatal exposure to methimazole
Methimazole is an antihyperthyroid drug used to treat hyperthyroidism, particularly Graves' disease. The drug reduces ...
18
Apr
Mitral valve atresia
Mitral atresia is a rare congenital heart defect in which the mitral valve is either absent or anatomically defective.
18
Apr
Muscle atrophy
Muscle atrophy is a pathological process characterized by a decrease in the volume of muscle tissue, which can lead to weakness, decreased...
18
Apr
Middle East Respiratory Syndrome (MERS)
Middle East respiratory syndrome (MERS) is an acute viral disease caused by the MERS-CoV coronavirus. The disease is charac...
18
Apr
Marchiafava Bignami disease
Marchiafava Bignami disease (or beta-thalassemia) is an inherited disorder characterized by a defect in the synthesis of protein...
18
Apr
Menetrier's disease
Menetrier's disease (or Menetrier's disease) is a rare but serious disorder of the stomach characterized by hypertrophy of the gastric mucosa...
18
Apr
Menkes disease
Menkes disease, or Menkes syndrome, is a rare inherited disorder characterized by a disorder of copper metabolism in...
18
Apr
Meniere's disease
Meniere's disease is a chronic, relapsing disorder of the inner ear characterized by attacks of vertigo, hearing loss, and...
18
Apr
Mikulicz's disease
Mikulicz disease, also known as Mikulicz's disease or lymphomatous edema, is a rare disorder characterized by...
18
Apr
Milroy's disease
Milroy disease, also known as hereditary lymphedema, refers to a group of disorders characterized by impaired lymphatic drainage,...
18
Apr
Mondor's disease
Mondor's disease, or Mondor's syndrome, is a rare condition characterized by inflammation of the veins under the skin in the chest area...
18
Apr
Microvillous inclusion disease
Microvillous inclusion disease (MVID) is a genetic disorder characterized by abnormal development of microvilli and loss of normal...
18
Apr
Minimal change disease
Minimal change disease (MCD) is one of the most common diseases leading to nephrotic syndrome...
18
Apr
Maple Syrup Urine Disease
Maple syrup urine disease (MSUD) is a rare inherited disorder that affects the urine of...
18
Apr
Moyamoya disease
Moyamoya disease is a rare inherited disorder characterized by progressive dysfunction of the respiratory and cardiovascular systems.
18
Apr
Major Depression
Major depression, also known as depressive disorder, is a complex mental illness characterized by...
18
Apr
Congenital myotonia
Congenital myotonia is a rare hereditary disorder characterized by dysfunction of skeletal muscles, manifested by...
18
Apr
Congenital hypotrichosis of Maria Unna
Maria Unna's congenital hypotrichosis is a rare genetic disorder that causes a lack of hair on the body and head. This condition...
18
Apr
Mycosis fungoides
Mycosis fungoides (graft-versus-host disease, GvHD) is a complex disease that is the body's immune response to transp...
18
Apr
Double upper lip
Double upper lip, also known as duplication or hypertrophy of the upper lip, is an anomaly characterized by...