Prolidase Deficiency

"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.

MeSH information

Definition | Details | More General Concepts | Related Concepts | More Specific Concepts

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

Below are MeSH descriptors whose meaning is more general than "Prolidase Deficiency".

Diseases [C]
Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16]
Congenital Abnormalities [C16.131]
Abnormalities, Multiple [C16.131.077]
Prolidase Deficiency [C16.131.077.735]
Skin Abnormalities [C16.131.831]
Prolidase Deficiency [C16.131.831.720]
Genetic Diseases, Inborn [C16.320]
Metabolism, Inborn Errors [C16.320.565]
Amino Acid Metabolism, Inborn Errors [C16.320.565.100]
Prolidase Deficiency [C16.320.565.100.794]
Skin Diseases, Genetic [C16.320.850]
Prolidase Deficiency [C16.320.850.746]

Below are MeSH descriptors whose meaning is related to "Prolidase Deficiency".

Below are MeSH descriptors whose meaning is more specific than "Prolidase Deficiency".

publications

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This graph shows the total number of publications written about "Prolidase Deficiency" by people in Harvard Catalyst Profiles by year, and whether "Prolidase Deficiency" was a major or minor topic of these publication.

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