von Hippel-Lindau Disease
"von Hippel-Lindau Disease" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus,
MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure,
which enables searching at various levels of specificity.
An autosomal dominant disorder caused by mutations in a tumor suppressor gene. This syndrome is characterized by abnormal growth of small blood vessels leading to a host of neoplasms. They include HEMANGIOBLASTOMA in the RETINA; CEREBELLUM; and SPINAL CORD; PHEOCHROMOCYTOMA; pancreatic tumors; and renal cell carcinoma (see CARCINOMA, RENAL CELL). Common clinical signs include HYPERTENSION and neurological dysfunctions.
| Descriptor ID |
D006623
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| MeSH Number(s) |
C10.562.925 C14.907.077.925
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| Concept/Terms |
von Hippel-Lindau Disease- von Hippel-Lindau Disease
- von Hippel Lindau Disease
- Familial Cerebello-Retinal Angiomatosis
- Angiomatoses, Familial Cerebello-Retinal
- Angiomatosis, Familial Cerebello-Retinal
- Cerebello-Retinal Angiomatoses, Familial
- Cerebello-Retinal Angiomatosis, Familial
- Familial Cerebello Retinal Angiomatosis
- Familial Cerebello-Retinal Angiomatoses
- Hippel-Lindau Disease
- Hippel Lindau Disease
- Lindau Disease
- von Hippel-Lindau Syndrome
- Syndrome, von Hippel-Lindau
- von Hippel Lindau Syndrome
- Angiomatosis Retinae
- Retinae, Angiomatosis
- VHL Syndrome
- Syndrome, VHL
- Syndromes, VHL
- VHL Syndromes
- Cerebelloretinal Angiomatosis, Familial
- Angiomatoses, Familial Cerebelloretinal
- Angiomatosis, Familial Cerebelloretinal
- Cerebelloretinal Angiomatoses, Familial
- Familial Cerebelloretinal Angiomatoses
- Familial Cerebelloretinal Angiomatosis
- Lindau's Disease
- Lindau's Diseases
- Lindaus Disease
|
Below are MeSH descriptors whose meaning is more general than "von Hippel-Lindau Disease".
Below are MeSH descriptors whose meaning is more specific than "von Hippel-Lindau Disease".
This graph shows the total number of publications written about "von Hippel-Lindau Disease" by people in this website by year, and whether "von Hippel-Lindau Disease" was a major or minor topic of these publications.
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| Year | Major Topic | Minor Topic | Total |
|---|
| 1998 | 1 | 0 | 1 |
| 2007 | 1 | 0 | 1 |
| 2009 | 1 | 0 | 1 |
| 2013 | 1 | 0 | 1 |
| 2017 | 1 | 0 | 1 |
| 2021 | 1 | 0 | 1 |
| 2023 | 2 | 0 | 2 |
| 2024 | 1 | 0 | 1 |
| 2025 | 1 | 0 | 1 |
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Below are the most recent publications written about "von Hippel-Lindau Disease" by people in Profiles.
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Update on Surveillance in Von Hippel-Lindau Disease. Clin Cancer Res. 2025 Jun 13; 31(12):2271-2277.
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A Cerebellar Tumor-to-Tumor Metastasis in a Patient With Von Hippel-Lindau Disease. Appl Immunohistochem Mol Morphol. 2024 May-Jun 01; 32(5):244-248.
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Neurocutaneous Disorders in Pregnancy. Obstet Gynecol Surv. 2023 Oct; 78(10):606-619.
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Guidelines for surveillance of patients with von Hippel-Lindau disease: Consensus statement of the International VHL Surveillance Guidelines Consortium and VHL Alliance. Cancer. 2023 10 01; 129(19):2927-2940.
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Therapeutically actionable signaling node to rescue AURKA driven loss of primary cilia in VHL-deficient cells. Sci Rep. 2021 05 17; 11(1):10461.
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Von Hippel-Lindau and Hereditary Pheochromocytoma/Paraganglioma Syndromes: Clinical Features, Genetics, and Surveillance Recommendations in Childhood. Clin Cancer Res. 2017 Jun 15; 23(12):e68-e75.
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The utility of cortical-sparing adrenalectomy in pheochromocytomas associated with genetic syndromes. J Pediatr Surg. 2013 Jun; 48(6):1422-5.
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Cystic renal neoplasms and renal neoplasms associated with cystic renal diseases in adults: cross-sectional imaging findings. J Comput Assist Tomogr. 2012 Nov-Dec; 36(6):659-68.
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Pancreatic endocrine neoplasms: a current update on genetics and imaging. Br J Radiol. 2012 Jun; 85(1014):682-96.
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Increased mobilisation of circulating endothelial progenitors in von Hippel-Lindau disease and renal cell carcinoma. Br J Cancer. 2011 Jun 28; 105(1):112-7.