Telangiectasia, Hereditary Hemorrhagic
"Telangiectasia, Hereditary Hemorrhagic" 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 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.
Descriptor ID |
D013683
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MeSH Number(s) |
C14.907.454.900 C14.907.823.780 C15.378.463.515.900 C16.131.240.850.968
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Concept/Terms |
Telangiectasia, Hereditary Hemorrhagic- Telangiectasia, Hereditary Hemorrhagic
- Hemorrhagic Telangiectasia, Hereditary
- Rendu-Osler-Weber
- Rendu Osler Weber
- Telangiectasia, Hereditary Hemorrhagic, of Rendu, Osler, and Weber
- Telangiectasia, Hereditary Hemorrhagic, Type 1
- Osler-Rendu Disease
- Osler Rendu Disease
- Osler-Rendu-Weber Disease
- Osler Rendu Weber Disease
- Hereditary Hemorrhagic Telangiectasia
- Osler's Disease
- Disease, Osler's
- Osler Disease
- Osler-Weber-Rendu Syndrome
- Osler Weber Rendu Syndrome
- Weber-Osler
- Weber Osler
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Below are MeSH descriptors whose meaning is more general than "Telangiectasia, Hereditary Hemorrhagic".
Below are MeSH descriptors whose meaning is more specific than "Telangiectasia, Hereditary Hemorrhagic".
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