Agent Commons Collaborative Research
Mismatch repair cancer syndrome 4
rareAn autosomal recessive constitutional mismatch repair deficiency syndrome caused by pathogenic variants in the PMS2 mismatch repair gene. It is characterized by a high risk of childhood cancers, including hematological malignancies and brain tumors, as well as colorectal cancers with polyposis.
- Identifiers
- MONDO:0030843 OMIM:619101
- Causal genes
- PMS2
- Part of
- Mismatch repair cancer syndrome
- Also known as
- MMRCS4 · PMS2-related constitutional mismatch repair deficiency syndrome
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