MLchartDataset catalogue

AFAP

Term · Oncology and biomedicine · MLC-T-ONC-000303

A rare, inherited disorder in which multiple polyps (abnormal growths) form on the inner walls of the colon and rectum. People with AFAP usually develop fewer than 100 polyps. Benign (not cancer) tumors may also occur in the stomach, small intestine, bone, skin, and soft tissue. People with AFAP have a very high risk of developing colorectal cancer and may also be at risk of developing cancers of the stomach, small intestine, liver, and breast. AFAP is caused by mutations (changes) in the APC gene that are inherited in an autosomal dominant manner. It is a type of hereditary cancer syndrome. Also called attenuated familial adenomatous polyposis.

Table 1. Record
IdentifierMLC-T-ONC-000303
FieldOncology and biomedicine
Expansionsattenuated familial adenomatous polyposis
ReferencesNCI Dictionary of Cancer Terms
Record as JSON
{
  "id": "MLC-T-ONC-000303",
  "term": "AFAP",
  "field": "Oncology and biomedicine",
  "definition": "A rare, inherited disorder in which multiple polyps (abnormal growths) form on the inner walls of the colon and rectum. People with AFAP usually develop fewer than 100 polyps. Benign (not cancer) tumors may also occur in the stomach, small intestine, bone, skin, and soft tissue. People with AFAP have a very high risk of developing colorectal cancer and may also be at risk of developing cancers of the stomach, small intestine, liver, and breast. AFAP is caused by mutations (changes) in the APC gene that are inherited in an autosomal dominant manner. It is a type of hereditary cancer syndrome. Also called attenuated familial adenomatous polyposis.",
  "expansions": [
    "attenuated familial adenomatous polyposis"
  ],
  "references": [
    "NCI Dictionary of Cancer Terms"
  ],
  "url": "https://mlchart.com/terminology/oncology/afap/"
}

Record 516 of 17,717 in Oncology and biomedicine terminology (MLC-0111). Request the full dataset.