Mismatch repair cancer syndrome 3

MONDO:0030841

An autosomal recessive constitutional mismatch repair deficiency syndrome caused by pathogenic variants in the MSH6 mismatch repair gene is characterized by a high risk of childhood cancers, including hematological malignancies, brain tumors, and colorectal

Also known as: MMRCS3, MSH6-related constitutional mismatch repair deficiency syndrome, mismatch repair cancer syndrome 3

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

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