Maxillary sinus neoplasm is a condition affecting the sinus within the facial region and can present as either a benign tumor, such as Schneiderian pa...

Maxillary sinus squamous cell carcinoma is a malignant tumor arising from the mucosal epithelial surface of the maxillary sinus in the head and neck r...

MAX-related tumor predisposition is an inherited condition caused by changes in the MAX gene. It is characterized by an increased risk of developing s...

Mayer-Rokitansky-Küster-Hauser (MRKH) syndrome type 1 is a rare condition where the uterus and two-thirds of the vagina are not present. This conditio...

Mayer-Rokitansky-Küster-Hauser syndrome type 2 is a rare condition present from birth in which people do not develop a uterus and the upper two-thirds...

May-Thurner syndrome is a condition where there is compression of the iliac vein. This compression reduces blood flow in the vein and in the left lowe...

Mazabraud syndrome is a rare bone condition that occurs when fibrous dysplasia, an abnormal growth of bone tissue, is seen together with intramuscular...

McCune-Albright syndrome (MAS) is a complex condition that primarily affects the bones, skin, and endocrine systems. It is classically defined by the...

MCD diffuse large B-cell lymphoma is a type of lymphoma that is categorized as MCD by the LymphGen algorithm. This categorization is based on several...

McDonough syndrome is a rare condition that includes several birth-related issues. People with this syndrome show differences in the shape and appeara...

McKusick-Kaufman syndrome is a very rare genetic developmental disorder. It is most often seen in the neonatal period and is characterized by malforma...

McLeod neuroacanthocytosis syndrome is a rare disorder that affects the brain and blood cells. It is part of a group of conditions known as neuroacant...

Meacham syndrome is a rare condition that affects several parts of the body. It is characterized by malformations that occur during development. Peopl...

Meckel diverticulum cancer is a type of cancer that occurs in a Meckel's diverticulum. A Meckel's diverticulum is a small pouch in the wall of the sma...

Meckel syndrome is a rare, lethal genetic disorder that causes multiple birth defects. People with this condition often have a combination of brain ma...

Meckel syndrome 13, also known as Meckel syndrome type 13 or MKS13, is a rare condition. Information about its overall characteristics is limited, but...

Meckel syndrome, type 1 is a rare genetic disorder that is caused by mutations in the MKS1 gene. It is also known by several other names including MKS...

Meckel syndrome, type 10 is a rare form of Meckel syndrome that is caused by a mutation in the B9D2 gene. This condition is part of a group of disorde...