MeSH Browser

MeSH Supplementary: Parotidomegaly, Hereditary Bilateral
Unique ID: C566821
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C566821
Registry Number: 0
Heading Mapped to: Parotid Gland / *abnormalities; *Genetic Diseases, Inborn
Frequency: 0
Date of Entry: 2012/11/05
Revision Date: 2013/11/06

Parotidomegaly, Hereditary Bilateral MeSH Supplementary Concept Data 2024