von Hippel-Lindau Disease [von Hippelova-Lindauova nemoc]
- Terms
-
angiomatosis retinae
Hippel-Lindauova choroba
Hippelova-Lindauova nemoc
Lindauova nemoc
retinální angiomatóza
VHL
von Hippelova-Lindauova choroba
von Hippelův-Lindauův syndrom
-
Angiomatosis Retinae
Cerebelloretinal Angiomatosis, Familial
Familial Cerebello-Retinal Angiomatosis
Hippel-Lindau Disease
Lindau Disease
Lindau's Disease
VHL Syndrome
von Hippel-Lindau Syndrome
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.
- DUI
- D006623 MeSH Browser
- CUI
- M0010373
- History note
- 2008 (1975)
- Public note
- 2008; see HIPPEL-LINDAU DISEASE 1991-2007; see ANGIOMATOSIS 1975-1990
Allowable subheadings
- BL
- blood 1
- CF
- cerebrospinal fluid
- CI
- chemically induced
- CL
- classification 2
- CO
- complications 7
- DI
- diagnosis 24
- DG
- diagnostic imaging 1
- DH
- diet therapy
- DT
- drug therapy
- EC
- economics
- EM
- embryology
- EN
- enzymology
- EP
- epidemiology 2
- EH
- ethnology
- ET
- etiology 5
- GE
- genetics 22
- HI
- history
- IM
- immunology
- ME
- metabolism
- MI
- microbiology
- MO
- mortality
- NU
- nursing
- PS
- parasitology
- PA
- pathology 10
- PP
- physiopathology 2
- PC
- prevention & control 1
- PX
- psychology
- RT
- radiotherapy
- RH
- rehabilitation
- SU
- surgery 4
- TH
- therapy 6
- UR
- urine
- VE
- veterinary
- VI
- virology