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VHL syndrome

Term · Oncology and biomedicine · MLC-T-ONC-009229

A rare, inherited disorder that causes tumors and cysts to grow in certain parts of the body, including the brain, spinal cord, eyes, inner ear, adrenal glands, pancreas, kidney, and reproductive tract. The tumors are usually benign (not cancer), but some may be malignant (cancer). Patients with VHL syndrome have an increased risk of certain types of cancer, especially kidney cancer and pancreatic cancer. The signs and symptoms of VHL syndrome usually do not appear until young adulthood. It is caused by a mutation (change) in the VHL gene. Also called VHL disease, von Hippel-Lindau disease, and von Hippel-Lindau syndrome.

Table 1. Record
IdentifierMLC-T-ONC-009229
FieldOncology and biomedicine
SynonymsVHL disease; von Hippel-Lindau disease; von Hippel-Lindau syndrome
ReferencesNCI Dictionary of Cancer Terms
Record as JSON
{
  "id": "MLC-T-ONC-009229",
  "term": "VHL syndrome",
  "field": "Oncology and biomedicine",
  "definition": "A rare, inherited disorder that causes tumors and cysts to grow in certain parts of the body, including the brain, spinal cord, eyes, inner ear, adrenal glands, pancreas, kidney, and reproductive tract. The tumors are usually benign (not cancer), but some may be malignant (cancer). Patients with VHL syndrome have an increased risk of certain types of cancer, especially kidney cancer and pancreatic cancer. The signs and symptoms of VHL syndrome usually do not appear until young adulthood. It is caused by a mutation (change) in the VHL gene. Also called VHL disease, von Hippel-Lindau disease, and von Hippel-Lindau syndrome.",
  "synonyms": [
    "VHL disease",
    "von Hippel-Lindau disease",
    "von Hippel-Lindau syndrome"
  ],
  "references": [
    "NCI Dictionary of Cancer Terms"
  ],
  "url": "https://mlchart.com/terminology/oncology/vhl-syndrome/"
}

Record 17,217 of 17,721 in Oncology and biomedicine terminology (MLC-0111). Request the full dataset.