 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
- von Hippel-Lindau Syndrome
- Syndrome, von Hippel-Lindau
- von Hippel Lindau Syndrome
- Lindau Disease
- Lindau's Disease
- Lindau's Diseases
- Lindaus Disease
- Cerebelloretinal Angiomatosis, Familial
- Angiomatoses, Familial Cerebelloretinal
- Angiomatosis, Familial Cerebelloretinal
- Cerebelloretinal Angiomatoses, Familial
- Familial Cerebelloretinal Angiomatoses
- Familial Cerebelloretinal Angiomatosis
- Hippel-Lindau Disease
- Hippel Lindau Disease
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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 UAMS Profiles by year, and whether "von Hippel-Lindau Disease" was a major or minor topic of these publications.
To see the data from this visualization as text, click here.
| Year | Major Topic | Minor Topic | Total |
|---|
| 2017 | 1 | 0 | 1 |
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Below are the most recent publications written about "von Hippel-Lindau Disease" by people in Profiles over the past ten years.
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Pichardo-Rojas PS, Tos SM, Mantziaris G, Shaaban A, Nabeel AM, Reda WA, Tawadros SR, AbdelKarim K, El-Shehaby AMN, Emad RM, Wei Z, McKendrick LM, Niranjan A, Lunsford LD, Peker S, Samanci Y, Liscak R, May J, Mathieu D, Lee CC, Yang HC, Dono A, Blanco AI, Esquenazi Y, Moreno NM, ?lvarez RM, Picozzi P, Franzini A, Tripathi M, Sumi T, Uzuka T, Kano H, Bailey D, Zacharia BE, Cifarelli CP, Cifarelli DT, Hack JD, Speckter H, Lazo E, Warnick RE, Schoenhals JE, Palmer JD, Xu Z, Sheehan JP. Safety and effectiveness of stereotactic radiosurgery for larger hemangioblastomas (>2cc): A multi-center retrospective study. PLoS One. 2026; 21(4):e0337000.
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Bellairs JA, Gluth MB. A histopathological connection between a fatal endolymphatic sac tumour and von Hippel-Lindau disease from 1960. J Laryngol Otol. 2018 Jan; 132(1):75-78.
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