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BAP1 tumor predisposition syndrome

Term · Oncology and biomedicine · MLC-T-ONC-000910

A rare inherited disorder that is caused by mutations (changes) in the BAP1 gene. Having this mutation increases the risk of developing certain types of cancerous tumors of the skin, eye, kidney, and mesothelium (the tissue that lines the chest and abdomen). The cancers tend to develop at an early age, are often fast-growing, and are more likely to spread to other parts of the body. Benign (not cancer) tumors of the skin may also occur. Not all people who have a mutation in the BAP1 gene will develop tumors.

Table 1. Record
IdentifierMLC-T-ONC-000910
FieldOncology and biomedicine
ReferencesNCI Dictionary of Cancer Terms
Record as JSON
{
  "id": "MLC-T-ONC-000910",
  "term": "BAP1 tumor predisposition syndrome",
  "field": "Oncology and biomedicine",
  "definition": "A rare inherited disorder that is caused by mutations (changes) in the BAP1 gene. Having this mutation increases the risk of developing certain types of cancerous tumors of the skin, eye, kidney, and mesothelium (the tissue that lines the chest and abdomen). The cancers tend to develop at an early age, are often fast-growing, and are more likely to spread to other parts of the body. Benign (not cancer) tumors of the skin may also occur. Not all people who have a mutation in the BAP1 gene will develop tumors.",
  "references": [
    "NCI Dictionary of Cancer Terms"
  ],
  "url": "https://mlchart.com/terminology/oncology/bap1-tumor-predisposition-syndrome/"
}

Record 3,275 of 17,717 in Oncology and biomedicine terminology (MLC-0111). Request the full dataset.