MeSH Browser

MeSH Heading: von Hippel-Lindau Disease
Tree Number(s): C10.562.925; C14.907.077.925; C16.131.077.245.750; C16.320.184.750
Unique ID: D006623
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/D006623
Scope Note: 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.
Entry Version: VON HIPPEL LINDAU DIS
Entry Term(s): Angiomatosis Retinae; Cerebelloretinal Angiomatosis, Familial; Familial Cerebello-Retinal Angiomatosis; Hippel-Lindau Disease; Lindau Disease; Lindau's Disease; VHL Syndrome; von Hippel-Lindau Syndrome
NLM Classification #: QS 677
Public MeSH Note: 2008; see HIPPEL-LINDAU DISEASE 1991-2007; see ANGIOMATOSIS 1975-1990
History Note: 2008 (1975)
Date Established: 1991/01/01
Date of Entry: 1999/01/01
Revision Date: 2017/12/14

Allowable Qualifiers: blood (BL)

cerebrospinal fluid (CF)

chemically induced (CI)

classification (CL)

complications (CO)

diagnosis (DI)

diagnostic imaging (DG)

diet therapy (DH)

drug therapy (DT)

economics (EC)

embryology (EM)

enzymology (EN)

epidemiology (EP)

ethnology (EH)

etiology (ET)

genetics (GE)

history (HI)

immunology (IM)

metabolism (ME)

microbiology (MI)

mortality (MO)

nursing (NU)

parasitology (PS)

pathology (PA)

physiopathology (PP)

prevention & control (PC)

psychology (PX)

radiotherapy (RT)

rehabilitation (RH)

surgery (SU)

therapy (TH)

urine (UR)

veterinary (VE)

virology (VI)

Concept UI: M0010373
Scope Note: 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.
Terms: von Hippel-Lindau Disease Preferred Term
Term UI T019933
Date10/24/1994
LexicalTag EPO
ThesaurusID; Familial Cerebello-Retinal Angiomatosis
Term UI T372184
Date11/08/1999
LexicalTag NON
ThesaurusID NLM (2000); Hippel-Lindau Disease
Term UI T019932
Date01/01/1999
LexicalTag EPO
ThesaurusID; VHL Syndrome
Term UI T844128
Date05/14/2013
LexicalTag ABX
ThesaurusID GHR (2014); Lindau's Disease
Term UI T372185
Date11/08/1999
LexicalTag NON
ThesaurusID NLM (2000); von Hippel-Lindau Syndrome
Term UI T372183
Date11/08/1999
LexicalTag EPO
ThesaurusID; Angiomatosis Retinae
Term UI T842671
Date04/18/2013
LexicalTag NON
ThesaurusID GHR (2014); Cerebelloretinal Angiomatosis, Familial
Term UI T372181
Date11/08/1999
LexicalTag NON
ThesaurusID; Lindau Disease
Term UI T372182
Date11/08/1999
LexicalTag EPO
ThesaurusID NLM (2000)

von Hippel-Lindau Disease MeSH Descriptor Data 2023