Glycogen Storage Disease Type III
"Glycogen Storage Disease Type III" 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 metabolic disorder due to deficient expression of amylo-1,6-glucosidase (one part of the glycogen debranching enzyme system). The clinical course of the disease is similar to that of glycogen storage disease type I, but milder. Massive hepatomegaly, which is present in young children, diminishes and occasionally disappears with age. Levels of glycogen with short outer branches are elevated in muscle, liver, and erythrocytes. Six subgroups have been identified, with subgroups Type IIIa and Type IIIb being the most prevalent.
Descriptor ID |
D006010
|
MeSH Number(s) |
C16.320.565.202.449.520 C18.452.648.202.449.520
|
Concept/Terms |
Glycogen Storage Disease Type III- Glycogen Storage Disease Type III
- Cori Disease
- Disease, Cori
- Cori's Disease
- Coris Disease
- Disease, Cori's
- Debrancher Deficiency
- Debrancher Deficiencies
- Deficiencies, Debrancher
- Deficiency, Debrancher
- Limit Dextrinosis
- Dextrinoses, Limit
- Dextrinosis, Limit
- Limit Dextrinoses
- Glycogen Debrancher Deficiency
- Debrancher Deficiencies, Glycogen
- Debrancher Deficiency, Glycogen
- Deficiencies, Glycogen Debrancher
- Deficiency, Glycogen Debrancher
- Glycogen Debrancher Deficiencies
- Glycogen Debranching Enzyme Deficiency
- Glycogen Storage Disease III
- Glycogen Storage Disease Type 3
- Glycogenosis 3
- Glycogenosis 3s
- Amylo-1,6-Glucosidase Deficiency
- Amylo 1,6 Glucosidase Deficiency
- Amylo-1,6-Glucosidase Deficiencies
- Deficiencies, Amylo-1,6-Glucosidase
- Deficiency, Amylo-1,6-Glucosidase
- Forbes Disease
- Disease, Forbes
|
Below are MeSH descriptors whose meaning is more general than "Glycogen Storage Disease Type III".
Below are MeSH descriptors whose meaning is more specific than "Glycogen Storage Disease Type III".
This graph shows the total number of publications written about "Glycogen Storage Disease Type III" by people in UAMS Profiles by year, and whether "Glycogen Storage Disease Type III" was a major or minor topic of these publications.
To see the data from this visualization as text, click here.
Year | Major Topic | Minor Topic | Total |
---|
2010 | 1 | 0 | 1 |
To return to the timeline, click here.
Below are the most recent publications written about "Glycogen Storage Disease Type III" by people in Profiles over the past ten years.
|
People People who have written about this concept. _
Similar Concepts
People who have written about this concept.
_
Top Journals
Top journals in which articles about this concept have been published.
|