Lynch syndrome
Term · Oncology and biomedicine · MLC-T-ONC-005056
An inherited disorder that increases the risk of developing colorectal cancer, endometrial cancer, ovarian cancer, and many other types of cancer, such as cancers of the stomach, small intestine, pancreas, bile duct, urinary tract, and brain, often before age 50. Lynch syndrome is caused by mutations (changes) in genes that affect DNA mismatch repair, a process that fixes mistakes that occur when DNA is copied. These genes are MLH1, MSH2, MSH6, PMS2, and EPCAM. Also called hereditary nonpolyposis colorectal cancer and HNPCC.
| Identifier | MLC-T-ONC-005056 |
|---|---|
| Field | Oncology and biomedicine |
| Synonyms | hereditary nonpolyposis colorectal cancer; HNPCC |
| References | NCI Dictionary of Cancer Terms |
Record as JSON
{
"id": "MLC-T-ONC-005056",
"term": "Lynch syndrome",
"field": "Oncology and biomedicine",
"definition": "An inherited disorder that increases the risk of developing colorectal cancer, endometrial cancer, ovarian cancer, and many other types of cancer, such as cancers of the stomach, small intestine, pancreas, bile duct, urinary tract, and brain, often before age 50. Lynch syndrome is caused by mutations (changes) in genes that affect DNA mismatch repair, a process that fixes mistakes that occur when DNA is copied. These genes are MLH1, MSH2, MSH6, PMS2, and EPCAM. Also called hereditary nonpolyposis colorectal cancer and HNPCC.",
"synonyms": [
"hereditary nonpolyposis colorectal cancer",
"HNPCC"
],
"references": [
"NCI Dictionary of Cancer Terms"
],
"url": "https://mlchart.com/terminology/oncology/lynch-syndrome/"
}
Record 10,491 of 17,717 in Oncology and biomedicine terminology (MLC-0111). Request the full dataset.