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A medulloblastoma is a brain tumor located in the cerebellum, the part of the brain that controls complex motor functions.

Meningioma is a slow-growing and usually non-cancerous tumor that originates in the meninges, the membrane layer covering the brain and spinal cord.

Multisystem inflammatory syndrome in children (MIS-C), also called pediatric multi-system inflammatory syndrome temporally related to SARS CoV-2 (PMIS or PIMS-TS), is a potentially serious illness in children that appears to...

Mucopolysarcharidosis type IVA (MPS IVA), also known as Morquio syndrome type A, is a rare, inherited disorder in which genetic variations disrupt the normal activity of lysosomes in human cells.

Mucopolysarcharidosis type VII (MPS VII), also known as Sly syndrome, is a rare, inherited disorder in which genetic variations disrupt the normal activity of lysosomes in human cells.

Mucolipidosis I (ML I), or sialidosis, is a rare, inherited disorder in which genetic variations disrupt the normal activity of lysosomes in human cells.

Mucolipidosis II (ML II), or I-cell disease, is a rare, inherited disorder in which genetic variations disrupt the normal activity of lysosomes in human cells.

Midaortic syndrome is a very rare condition in which part of the aorta that runs through the chest and abdomen narrows.

A milk allergy is an abnormal response of the body to the proteins found in cows’ milk.

Mitral valve stenosis happens when the mitral valve is too narrow, causing blood to back up in the heart’s left atrium.