MeSH Browser

MeSH Supplementary: Hyperinsulinism, autosomal recessive
Unique ID: C538567
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C538567
Registry Number: 0
Heading Mapped to: *Nesidioblastosis
Frequency: 1
Note: Persistent hyperinsulinemic hypoglycemia of infancy due to focal adenomatous hyperplasia
Date of Entry: 2010/08/25
Revision Date: 2012/08/24

Hyperinsulinism, autosomal recessive MeSH Supplementary Concept Data 2024