List of MeSH codes (C16)

List of MeSH Codes (C16) refers to a comprehensive index of MeSH (Medical Subject Headings) codes that are specifically categorized under the section C16, which deals with congenital, hereditary, and neonatal diseases and abnormalities. These codes are crucial for the organization, retrieval, and analysis of biomedical and health-related information. MeSH is a highly structured and controlled vocabulary used by the National Library of Medicine (NLM) to index articles for the PubMed database and other resources.

Overview

The C16 category encompasses a wide range of conditions and disorders that are present at birth or develop during the neonatal period. These can include genetic diseases, congenital abnormalities, inborn errors of metabolism, and other conditions that affect newborns. The classification under this category aids researchers, clinicians, and students in locating relevant literature and resources efficiently.

Structure of MeSH Codes (C16)

MeSH codes under category C16 are divided into several subcategories to cover the broad spectrum of congenital, hereditary, and neonatal diseases and abnormalities. Each subcategory is assigned a unique identifier, which helps in the precise indexing of medical subjects. Some of the notable subcategories include:

- C16.131 - Congenital Abnormalities - C16.320 - Genetic Diseases, Inborn - C16.614 - Infant, Newborn, Diseases - C16.131.939 - Vascular Malformations

Importance of MeSH Codes

MeSH codes play a vital role in the field of medical research and healthcare information management. They allow for the standardized classification of medical literature, making it easier to search for and retrieve specific information. The use of MeSH codes enhances the accuracy and efficiency of literature searches, which is essential for evidence-based medicine, research, and education.

Accessing MeSH Codes

MeSH codes can be accessed through the National Library of Medicine's website or directly through the PubMed search interface. Researchers and healthcare professionals can use these codes to refine their literature searches, ensuring that they retrieve the most relevant and specific information for their needs.

Conclusion

The List of MeSH Codes (C16) is an essential resource for anyone involved in the study or treatment of congenital, hereditary, and neonatal diseases and abnormalities. By providing a structured and comprehensive classification system, MeSH codes facilitate the efficient retrieval and analysis of biomedical information, contributing to advancements in medical research and patient care.