"Prolidase Deficiency" 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.
Rare autosomal recessive disorder of metabolism due to mutations in the prolidase gene. It is characterized by recurrent lower extremity skin ulcers, recurrent infections, and FACIES, often with INTELLECTUAL DISABILITY.
| Descriptor ID |
D056732
|
| MeSH Number(s) |
C16.131.077.735 C16.131.831.720 C16.320.565.100.794 C16.320.850.746
|
| Concept/Terms |
Prolidase Deficiency- Prolidase Deficiency
- Deficiencies, Prolidase
- Deficiency, Prolidase
- Prolidase Deficiencies
- Imidodipeptidase Deficiency
- Deficiencies, Imidodipeptidase
- Deficiency, Imidodipeptidase
- Imidodipeptidase Deficiencies
- Hyperimidodipeptiduria
- Hyperimidodipeptidurias
|
Below are MeSH descriptors whose meaning is more general than "Prolidase Deficiency".
Below are MeSH descriptors whose meaning is more specific than "Prolidase Deficiency".
This graph shows the total number of publications written about "Prolidase Deficiency" by people in this website by year, and whether "Prolidase Deficiency" 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 |
|---|
| 2017 | 1 | 0 | 1 |
To return to the timeline, click here.
Below are the most recent publications written about "Prolidase Deficiency" by people in Profiles.
-
Hyperbaric oxygen therapy in the management of severe leg ulcers from prolidase deficiency. BMJ Case Rep. 2017 Jan 06; 2017.