Mixed phenotype acute leukemia, B/myeloid is an aggressive hematologic malignancy characterized by the presence of blasts that express both B-lymphoid...

Mixed teratoma and seminoma is a type of tumor that exhibits features of both teratoma and seminoma, representing a mixed germ cell neoplasm. Although...

Mixed testicular germ cell cancer is a malignant tumor arising from the testis and is characterized by the presence of more than one histologic compon...

Miyoshi muscular dystrophy 1 is a type of muscular dystrophy caused by a mutation in the DYSF gene. This condition is part of a group of disorders ref...

Miyoshi muscular dystrophy 2 is a rare genetic condition that affects the muscles. It is also known by several names, including MMD2, MIYOSHI muscular...

Miyoshi muscular dystrophy 3 is a rare condition with limited detailed definition available through current sources. It is also known by other names s...

Miyoshi myopathy is a type of muscle condition that mainly affects the muscles in the lower legs, particularly the calf muscles such as the gastrocnem...

MKKS-related ciliopathy is a term used to describe any ciliopathy caused by variants in the MKKS gene. Ciliopathies are a group of conditions in which...

MKS1-related ciliopathy is a rare condition caused by changes in the MKS1 gene. This gene is important for the function of cilia, which are small, hai...

MMEP syndrome is a rare congenital condition that affects the development of several parts of the body. It is a syndromic form of split-hand/foot malf...

Currently, MME-related autosomal dominant Charcot Marie Tooth disease type 2 (CMT2) lacks a defined genetic basis, and the inheritance pattern remains...

Mobitz type II atrioventricular block is a cardiac conduction disorder characterized by intermittent failure of atrial electrical impulses to reach th...

Mobius syndrome is a very rare condition that people are born with. It is known for causing complete or partial paralysis of the face, meaning that th...