Disease Directory

Mononen-Karnes-Senac syndrome is a rare condition that affects the skeleton. This syndrome is mainly characterized by abnormalities in the hands and f...

Mooren ulcer, also known as Mooren's ulcer, is recognized as a rare condition. This disease is catalogued by international resources such as Orphanet...

Morgagni-Stewart-Morel syndrome is a condition where there is a thickening of the inner table of the frontal bone. This thickening is sometimes associ...

Morimoto-Ryu-Malicdan neuromuscular syndrome is a rare disorder that has been associated with the RFC4 gene. It is categorized as a neuromuscular cond...

Morquio syndrome C, also known as Morquio syndrome type C or Nonkeratosulfate-Excreting type, is a rare condition that has been cataloged in genetic d...

Morvan syndrome is a rare and life-threatening acquired neurological disease. It is marked by a mix of symptoms affecting the central nervous system,...

Mounier-Kuhn syndrome, also known as idiopathic tracheobronchomegaly, is a congenital disorder where the trachea and the main bronchi are markedly enl...

Mowat-Wilson syndrome is a multisystem genetic condition that combines distinctive facial features with significant developmental and neurological cha...

Mowat-Wilson syndrome due to a ZEB2 point mutation is a rare genetic condition. It is also known as Hirschsprung disease and intellectual disability d...

Mowat-Wilson syndrome due to monosomy 2q22 is a rare condition that has been described with several different names, including Hirschsprung disease an...

Moyamoya disease is a rare intracranial arteriopathy characterized by progressive narrowing of the arteries at the base of the brain. This vascular co...

Moyamoya disease 2 is a rare form of Moyamoya disease in which changes occur in the blood vessels of the brain. This condition is caused by a mutation...

Moyamoya disease 5 is a rare form of Moyamoya disease that is uniquely linked to a mutation in the ACTA2 gene. This subtype is defined by its genetic...

Moyamoya disease with early-onset achalasia is an exceedingly rare neurological disorder that has been reported in only a few families. It is inherite...

Moynahan syndrome is a rare inherited condition that affects various parts of the body. It is defined as a Mendelian condition, meaning it is passed d...

Muckle-Wells syndrome is an intermediate form of a group of disorders known as cryopyrin-associated periodic syndromes (CAPS). People with this condit...

Muenke syndrome is a type of craniosynostosis where the bones in the skull fuse sooner than usual. This early fusion typically affects the coronal sut...

Muir-Torre syndrome is a hereditary condition that is considered a variant of hereditary nonpolyposis colon cancer (HNPCC). It is characterized by the...

Mycobacterium xenopi infection is a disease caused by an infection with the bacterium Mycobacterium xenopi. This condition is identified when people d...

Mycoplasma encephalitis is a rare brain infection caused by the bacterium Mycoplasma pneumoniae. It is marked by an acute onset of neurological signs...