Lipoid Proteinosis of Urbach and Wiethe
"Lipoid Proteinosis of Urbach and Wiethe" 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 recessive disorder characterized by glassy degenerative thickening (hyalinosis) of SKIN; MUCOSA; and certain VISCERA. This disorder is caused by mutation in the extracellular matrix protein 1 gene (ECM1). Clinical features include hoarseness and skin eruption due to widespread deposition of HYALIN.
| Descriptor ID |
D008065
|
| MeSH Number(s) |
C08.618.490.500 C16.320.850.595
|
| Concept/Terms |
Lipoid Proteinosis of Urbach and Wiethe- Lipoid Proteinosis of Urbach and Wiethe
- Lipoidproteinosis
- Urbach-Wiethe Syndrome
- Urbach-Wiethe Disease
- Urbach Wiethe Disease
- Urbach-Wiethe Lipoid Proteinosis
- Lipoid Proteinosis, Urbach-Wiethe
- Urbach Wiethe Lipoid Proteinosis
- Hyalinosis Cutis et Mucosae
- Lipoproteinosis
|
Below are MeSH descriptors whose meaning is more general than "Lipoid Proteinosis of Urbach and Wiethe".
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