MeSH Browser

MeSH Supplementary: Pancreatic Agenesis, Congenital
Unique ID: C564908
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C564908
Entry Term(s): Pancreatic Hypoplasia, Congenital
Registry Number: 0
Heading Mapped to: Pancreas / *abnormalities; Pancreatic Diseases / *congenital
Frequency: 15
Date of Entry: 2012/11/05
Revision Date: 2013/11/06

Pancreatic Agenesis, Congenital MeSH Supplementary Concept Data 2024