Structured Summary
Abstract
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.
MeSH Record
Classification
Related Concepts
Knowledge Graph
Drag nodes to rearrange; hover to trace links; click a node to open its page.
MeSH Record
Synonyms
9 entry terms
- Hyperimidodipeptiduria
- Imidodipeptidase Deficiency
- Deficiencies, Imidodipeptidase
- Deficiencies, Prolidase
- Deficiency, Imidodipeptidase
- Deficiency, Prolidase
- Hyperimidodipeptidurias
- Imidodipeptidase Deficiencies
- Prolidase Deficiencies
MeSH Record
Aspects Covered
34 allowable subheadings
Indexed with the subheadings blood, cerebrospinal fluid, chemically induced, classification, complications, diagnosis, diagnostic imaging, diet therapy, drug therapy, economics, embryology, enzymology, epidemiology, ethnology, etiology, genetics, history, immunology, metabolism, microbiology, mortality, nursing, parasitology, pathology, physiopathology, prevention & control, psychology, radiotherapy, rehabilitation, surgery, therapy, urine, veterinary, virology.
MeSH Record
History Note
2010
MeSH Record
Previous Indexing
- Dipeptidases (1972-2009)
MeSH Hierarchy
Tree Numbers
AMA Style
References
- National Library of Medicine. Prolidase Deficiency. Medical Subject Headings (MeSH). 2026. Unique ID D056732. http://id.nlm.nih.gov/mesh/2026/D056732
- Prolidase Deficiency. In: Wikipedia. https://en.wikipedia.org/wiki/Prolidase_deficiency
- Prolidase Deficiency. In: Wikidata. https://www.wikidata.org/wiki/Q7249599