Mismatch repair cancer syndrome 2

MONDO:0030840

An autosomal recessive constitutional mismatch repair deficiency syndrome caused by pathogenic variants in the MSH2 mismatch repair gene. It is characterized by a high risk of many different types of childhood cancers, including hematological malignancies, brain tumors, intestinal polyposis, and colon cancer.

Also known as: MMRCS2, MSH2-related constitutional mismatch repair deficiency syndrome, mismatch repair cancer syndrome 2

26 clinical trials for this condition and its sub-types.

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