Explore 10,888+ rare diseases with trusted, clear information
Medical professionals review and validate information.
Expert Stewards stand behind their work.
Patients and families contribute real-world insights.
Showing 1,641-1,660 of 15,964 diseases
MONDO:0957477
MYT1L-related developmental delay-intellectual disability-obesity syndrome is a rare condition listed in Orphanet (Orphanet:647799). The name of the c...
MONDO:0007182
Machado-Joseph disease, also known as spinocerebellar ataxia type 3 (SCA3), is a rare neurodegenerative disorder. It is the most common subtype of typ...
MONDO:0017174
Machado-Joseph disease type 1 is a rare and often severe subtype of Machado-Joseph disease, which is also known as spinocerebellar ataxia type 3 or SC...
MONDO:0017175
Machado-Joseph disease type 2 is a subtype of Machado-Joseph disease (SCA3/MJD) that is known for its intermediate severity. People with this conditio...
MONDO:0017176
Machado-Joseph disease type 3 is a subtype of Machado-Joseph disease (also known as SCA3 or Machado type) that tends to be milder compared to other su...
MONDO:0042964
Machado-Joseph disease type 4 is a rare subtype of Machado-Joseph disease, also known as the azorean disease or type iv. This condition is marked by P...
MONDO:0018154
Madelung deformity is a condition that affects the wrist. It is characterized by abnormalities in the bones of the forearm, mainly involving shortened...
MONDO:0017557
Information about overview is currently limited for this condition.
MONDO:0017556
Madelung deformity, unilateral is a rare condition that affects the wrist. The current medical literature provides limited details about its exact def...
MONDO:0015307
Madras motor neuron disease (MMND) is a rare condition that primarily affects the nerves controlling the muscles of the limbs and several cranial nerv...
MONDO:0013808
Maffucci syndrome is a very rare genetic bone and skin disorder. It is characterized by the presence of multiple enchondromas, which are benign cartil...
MONDO:0012316
Majeed syndrome is a rare genetic multisystemic disorder characterized by three main features: chronic recurrent multifocal osteomyelitis, congenital...
MONDO:0013885
Malan overgrowth syndrome is a rare multisystem genetic disorder characterized by distinctive facial features, macrocephaly, and overgrowth in infancy...
MONDO:0020959
Mansonella ozzardi infection is an illness caused by a parasite called Mansonella ozzardi. This condition is classified as a parasitic infection and f...
MONDO:0859147
Marbach-Rustad progeroid syndrome is a rare condition that has been noted to show signs of premature aging in affected individuals. It is also known b...
MONDO:0859214
Marbach-Schaaf neurodevelopmental syndrome is a condition that primarily affects neurological development and function. It is associated with pathogen...
MONDO:0016429
Marburg acute multiple sclerosis is a rare and aggressive variant of multiple sclerosis. It is characterized by a rapidly progressive course and featu...
MONDO:0020500
Marburg hemorrhagic fever is a severe viral illness caused by the Marburg virus. People with this condition often start with a high fever and a genera...
MONDO:0016370
Marchiafava-Bignami disease is a rare neurological condition that mainly affects people with a history of severe, chronic alcoholism. It is characteri...
MONDO:0009564
Marden-Walker syndrome is a malformation syndrome that affects several parts of the body. People with this condition often have a mask-like face with...