Moderate hypophosphatasia is a rare condition that impairs the mineralization of bone and teeth, leading to defective bone formation and premature los...

Moderately severe hemophilia A is a blood clotting disorder characterized by a deficiency in factor VIII, which leads to abnormal bleeding even after...

Moderately severe hemophilia B is characterized by a deficiency in factor IX, leading to abnormal bleeding, particularly after minor injuries or surgi...

Moderate multiminicore disease with hand involvement is a condition that appears to affect skeletal muscle function, with a particular emphasis on the...

Moebius syndrome-axonal neuropathy-hypogonadotropic hypogonadism syndrome is a rare condition that brings together features of Moebius syndrome and ad...

MOGS-congenital disorder of glycosylation (MOGS-CDG) is a type of congenital disorder affecting N-linked glycosylation, a process that helps form prot...

Mollaret’s meningitis is a rare clinical disorder characterized by at least three episodes of meningitis. People with this condition often experience...

MOMO syndrome is a very rare genetic condition that leads to overgrowth and obesity. People with this syndrome may have a large head (macrocephaly), h...

Monoclonal gammopathy is a condition defined by the abnormal presence of a single type of immunoglobulin in the blood or urine. It is not known to be...

Monoclonal gammopathy of uncertain significance (MGUS) is a condition characterized by the presence of an abnormal monoclonal protein in the blood wit...

Monoclonal mast cell activation syndrome, also known as primary MCAS, is a condition characterized by the abnormal activation and clonal expansion of...

Monoclonal paraproteinemia disease is a hematologic condition characterized by the presence of excessive amounts of a single type of immunoglobulin in...

Monocytic leukemia is a malignant cancer of the blood that arises from cells of the immune system, specifically those in the monocytic lineage. The co...

Monogenic alpha thalassemia spectrum is an inherited blood condition resulting from a monogenomic modification. Although the precise genetic details h...