HNPCC
Term · Oncology and biomedicine · MLC-T-ONC-003939
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. HNPCC 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 Lynch syndrome.
| Identifier | MLC-T-ONC-003939 |
|---|---|
| Field | Oncology and biomedicine |
| Expansions | hereditary nonpolyposis colorectal cancer; Lynch syndrome |
| References | NCI Dictionary of Cancer Terms |
Record as JSON
{
"id": "MLC-T-ONC-003939",
"term": "HNPCC",
"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. HNPCC 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 Lynch syndrome.",
"expansions": [
"hereditary nonpolyposis colorectal cancer",
"Lynch syndrome"
],
"references": [
"NCI Dictionary of Cancer Terms"
],
"url": "https://mlchart.com/terminology/oncology/hnpcc/"
}
Record 8,585 of 17,721 in Oncology and biomedicine terminology (MLC-0111). Request the full dataset.