hereditary nonpolyposis colorectal cancer
Term · Oncology and biomedicine · MLC-T-ONC-003848
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. Hereditary nonpolyposis colorectal cancer 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 HNPCC and Lynch syndrome.
| Identifier | MLC-T-ONC-003848 |
|---|---|
| Field | Oncology and biomedicine |
| Synonyms | HNPCC; Lynch syndrome |
| References | NCI Dictionary of Cancer Terms |
Record as JSON
{
"id": "MLC-T-ONC-003848",
"term": "hereditary nonpolyposis colorectal cancer",
"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. Hereditary nonpolyposis colorectal cancer 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 HNPCC and Lynch syndrome.",
"synonyms": [
"HNPCC",
"Lynch syndrome"
],
"references": [
"NCI Dictionary of Cancer Terms"
],
"url": "https://mlchart.com/terminology/oncology/hereditary-nonpolyposis-colorectal-cancer/"
}
Record 8,450 of 17,721 in Oncology and biomedicine terminology (MLC-0111). Request the full dataset.