MeSH Browser

MeSH Heading: Telangiectasia, Hereditary Hemorrhagic
Tree Number(s): C14.907.454.900; C14.907.823.780; C15.378.463.515.900; C16.131.240.850.968
Unique ID: D013683
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/D013683
Scope Note: An autosomal dominant vascular anomaly characterized by telangiectases of the skin and mucous membranes and by recurrent gastrointestinal bleeding. This disorder is caused by mutations of a gene (on chromosome 9q3) which encodes endoglin, a membrane glycoprotein that binds TRANSFORMING GROWTH FACTOR BETA.
Entry Term(s): Hereditary Hemorrhagic Telangiectasia; Osler's Disease; Osler-Rendu Disease; Osler-Rendu-Weber Disease; Osler-Weber-Rendu Syndrome; Rendu-Osler-Weber Disease; Telangiectasia, Hereditary Hemorrhagic, Type 1; Telangiectasia, Hereditary Hemorrhagic, of Rendu, Osler, and Weber; Weber-Osler Disease; Weber-Osler Syndrome
NLM Classification #: WG 700
Public MeSH Note: 1968; for OSLER-RENDU DISEASE see ANGIOMATOSIS 1963-1967
History Note: 1968(1966); for OSLER-RENDU DISEASE use ANGIOMATOSIS 1963-1967
Date Established: 1968/01/01
Date of Entry: 1999/01/01
Revision Date: 2019/05/17

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)

Cardiovascular Diseases [C14]
- Vascular Diseases [C14.907]
  - Hemostatic Disorders [C14.907.454]

Cardiovascular Diseases [C14]
- Vascular Diseases [C14.907]
  - Telangiectasis [C14.907.823]

Hemic and Lymphatic Diseases [C15]
- Hematologic Diseases [C15.378]
  - Hemorrhagic Disorders [C15.378.463]
    - Hemostatic Disorders [C15.378.463.515]

Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16]
- Congenital Abnormalities [C16.131]
  - Cardiovascular Abnormalities [C16.131.240]
    - Vascular Malformations [C16.131.240.850]

Telangiectasia, Hereditary Hemorrhagic Preferred

Concept UI: M0021123
Scope Note: An autosomal dominant vascular anomaly characterized by telangiectases of the skin and mucous membranes and by recurrent gastrointestinal bleeding. This disorder is caused by mutations of a gene (on chromosome 9q3) which encodes endoglin, a membrane glycoprotein that binds TRANSFORMING GROWTH FACTOR BETA.
Terms: Telangiectasia, Hereditary Hemorrhagic Preferred Term
Term UI T040224
Date01/01/1999
LexicalTag NON
ThesaurusID; Telangiectasia, Hereditary Hemorrhagic, of Rendu, Osler, and Weber
Term UI T781718
Date12/06/2010
LexicalTag EPO
ThesaurusID; Rendu-Osler-Weber Disease
Term UI T000956382
Date04/30/2019
LexicalTag EPO
ThesaurusID NLM (2020); Osler-Weber-Rendu Syndrome
Term UI T752650
Date06/11/2009
LexicalTag EPO
ThesaurusID; Hereditary Hemorrhagic Telangiectasia
Term UI T841598
Date04/18/2013
LexicalTag NON
ThesaurusID GHR (2014); Osler's Disease
Term UI T841599
Date04/18/2013
LexicalTag EPO
ThesaurusID GHR (2014); Weber-Osler Syndrome
Term UI T000956383
Date04/30/2019
LexicalTag EPO
ThesaurusID NLM (2020); Osler-Rendu Disease
Term UI T040223
Date03/30/1974
LexicalTag EPO
ThesaurusID; Weber-Osler Disease
Term UI T000956381
Date04/30/2019
LexicalTag EPO
ThesaurusID NLM (2020); Osler-Rendu-Weber Disease
Term UI T680057
Date08/23/2006
LexicalTag EPO
ThesaurusID

Telangiectasia, Hereditary Hemorrhagic, Type 1 Narrower

Telangiectasia, Hereditary Hemorrhagic MeSH Descriptor Data 2024