Directory
Monomelic amyotrophy
Monomelic amyotrophy, also known as Benedict's syndrome, is a rare neurological disorder characterized by...
Mononeuritis multiplex
Mononeuritis multiplex is a pathological condition in which inflammation of several peripheral nerves occurs...
Mononucleosis
Mononucleosis is a viral disease caused by the Epstein-Barr virus (EBV), a member of the herpesvirus family. The main charac...
Male pseudohermaphroditism with gynecomastia
Male pseudohermaphroditism with gynecomastia is a rare endocrine disorder in which men exhibit signs of...
Mucolipidosis 3
Mucolipidosis 3, also known as Cornell disease, is a group of rare inherited metabolic disorders characterized by...
Mucolipidosis type 4
Mucolipidosis type 4 (ML4) is a rare inherited disorder that belongs to a group of mucolipidoses, which are...
Mucopolysaccharidosis type 1 (MPS I, Hurler syndrome)
Mucopolysaccharidosis type 1 (MPS I), also known as Hurler syndrome, is a rare inherited disorder that is related to...
Mucopolysaccharidosis type 2 (MPS II, Hunter syndrome)
Mucopolysaccharidosis type 2 (MPS II, Hunter syndrome) is a hereditary disease caused by a deficiency of a specific...
Mucopolysaccharidosis type 3 (MPS III, Sanfilippo syndrome)
Mucopolysaccharidosis type 3, also known as Sanfilippo syndrome, is a rare genetic disorder that affects the g...
Mucopolysaccharidosis type 4 (MPS IV, Morquio syndrome)
Mucopolysaccharidosis type 4 (MPS IV), also known as Morquio syndrome, is a rare genetic disorder that is related to ...
Mucopolysaccharidosis type 3B (MPS IIIB, Sanfilippo syndrome B)
Mucopolysaccharidosis type 3B (MPS IIIB, Sanfilippo syndrome B) is an inherited metabolic disorder related to ...
Mucopolysaccharidosis type 3A (MPS IIIA, Sanfilippo A syndrome)
Mucopolysaccharidosis type 3A (MPS IIIA), also known as Sanfilippo A syndrome, is an inherited metabolic disorder that...
Mucopolysaccharidosis type 4A (MPS IVA, Morquio syndrome type A)
Mucopolysaccharidosis type 4A (MPS IVA), also known as Morquio syndrome type A, is a rare inherited disorder that...
Mucopolysaccharidosis type 6 (MPS VI, Maroteaux-Lamy syndrome)
Mucopolysaccharidosis type 6 (MPS VI), also known as Maroteaux-Lamy syndrome, is a rare genetic disorder that is related to...
Mucopolysaccharidosis type 7 (MPS VII, Sly syndrome)
Mucopolysaccharidosis type 7 (MPS VII), also known as Sly syndrome, is a rare genetic disorder characterized by a deficiency of...
Mucopolysaccharidoses (MPS)
Mucopolysaccharidoses (MPS) are a group of rare hereditary diseases caused by metabolic disorders of mucopolysaccharides...
Mucormycosis
Mucormycosis (mucormycosis) is a serious and potentially life-threatening infection caused by fungi of the genus Mucor. These fungi...
Mulibrey Dwarfism
Mulibrey Dwarfism, or pituitary dwarfism, is a rare endocrine disorder associated with a deficiency of growth hormones...
Multisystem inflammatory syndrome in children (MIS-C)
Multisystem inflammatory syndrome in children (MIS-C) is a rare but potentially serious condition that involves...
Multifocal motor neuropathy
Multifocal motor neuropathy (MMN) is a rare disorder of the peripheral nervous system characterized by symme...
Multifocal atrial tachycardia
Multifocal atrial tachycardia (MAT) is a rare but clinically significant condition characterized by a high heart rate...
Multifocal fibrosclerosis
Multifocal fibrosclerosis (MFS) is a rare disease characterized by multiple fibrotic changes in different areas of the body.
Multicentric reticulohistiocytosis
Multicentric reticulohistiocytosis (MRH) is a rare hematological disorder characterized by proliferation of reticulohistiocyt...
Muscle invasive bladder cancer
Muscle-invasive bladder cancer (MIBC) is one of the most aggressive forms of bladder surface cancer, characterized by...
Muscle contracture Ehlers-Danlos syndrome (mcEDS)
Muscle contracture Ehlers-Danlos syndrome (mcEDS) is a rare inherited disorder of connective tissue characterized by...
Muscle spasms
Muscle spasms are involuntary and often painful contractions of muscles that occur as a result of a variety of ...
Müllerian aplasia
Müllerian aplasia, also known as Müller syndrome, is a congenital disorder that belongs to a group of developmental anomalies...
Morton's neuroma
Morton's neuroma is a benign tumor that occurs in the area of the interdigital nerves of the foot, most often between the th...
Malnutrition
Malnutrition is a condition in which there is a deficiency of nutrients needed to maintain normal functioning of the body.
Monkey pox
Monkeypox is a viral disease caused by the monkeypox virus, a member of the Orthopoxvirus family. Pathogen...
