MIRAGE syndrome is a rare, autosomal dominant condition caused by changes in the SAMD9 gene. People with this condition may experience a range of symp...

Mirizzi syndrome is a rare condition that happens as a complication of cholelithiasis (gallstone disease). It occurs when gallstones block or press on...

Mismatch repair cancer syndrome is a rare childhood cancer predisposition disorder that increases the risk of developing various malignancies at an ea...

Mismatch repair cancer syndrome 1 is an autosomal recessive condition caused by pathogenic variants in the MLH1 gene, which is vital for repairing DNA...

Mismatch repair cancer syndrome 4 is an inherited condition that increases the risk of developing several types of cancer during childhood. This condi...

Mitchell syndrome is a rare peroxisomal disorder. People with this condition experience episodes where the protective covering of nerve fibers in the...

MIT family translocation renal cell carcinoma is a rare subtype of kidney cancer. It is characterized by genetic changes, specifically rearrangements...

Mitochondrial complex 2 deficiency, nuclear type 2 is a disorder that primarily affects the nervous system and growth, leading to significant neurolog...