Myeloperoxidase deficiency is a rare genetic disorder affecting the immune system, primarily impacting the function of neutrophils. It is caused by ch...

Myelophthisic anemia is an aplastic anemia characterized by the replacement of normal bone marrow tissue with fibrotic tissue, tumors, or granulomas,...

Myeloproliferative disease, autosomal recessive is a condition characterized by abnormal proliferation in blood cell production. The precise underlyin...

Myeloproliferative disorder, chronic, with eosinophilia is a condition involving the abnormal proliferation of blood cell lineages, with a particular...

Myeloproliferative neoplasm is a clonal hematopoietic stem cell disorder in which one or more blood cell lineages are produced in excess in the bone m...

Myeloproliferative neoplasm, unclassifiable is a type of blood cancer that falls under the broad category of myeloproliferative neoplasms, where the c...

MYH10-related neurodevelopmental disorder with congenital anomalies is a rare genetic condition that affects brain development and may present with va...

MYH7-related skeletal myopathy is a rare autosomal dominant condition that primarily affects the muscles of the hands, feet, and neck. It is character...

Myhre syndrome is a multisystem connective tissue disorder that primarily affects growth, musculature, and the skeletal system. It is characterized by...

Myiasis is an infestation of human tissue by fly larvae, most commonly occurring in tropical climates. The condition typically affects the skin, parti...

Information about overview is currently limited for this condition.

Myocarditis is an inflammatory condition affecting the heart muscle, often resulting in symptoms such as chest pain, abnormal heart rhythms, or shortn...

Myoclonic cerebellar dyssynergia is a rare condition that mostly affects adults in their third decade of life or later. It is marked by a gradual loss...

Myoclonic dystonia 11 is a movement disorder characterized by a combination of involuntary muscle contractions and sudden jerking movements. It is cau...

Myoclonic dystonia 15 is a movement disorder characterized by involuntary muscle jerks and abnormal posturing, with a material basis in variation in t...

Myoclonic dystonia 26 is a neurological condition characterized primarily by involuntary muscle jerks (myoclonus) and sustained muscle contractions (d...

Myoclonic encephalopathy in non-progressive disorder is a group of epilepsies characterized by the early onset of seizures, often beginning from the f...

Myoclonic epilepsy is a group of epilepsy syndromes in which myoclonic seizures are a prominent clinical feature. It affects the nervous system and is...