MeSH Browser

MeSH Supplementary: Hyperbilirubinemia, Transient Familial Neonatal
Unique ID: C562692
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C562692
Registry Number: 0
Heading Mapped to: *Hyperbilirubinemia, Hereditary; *Hyperbilirubinemia, Neonatal
Frequency: 2
Date of Entry: 2012/11/05

Hyperbilirubinemia, Transient Familial Neonatal MeSH Supplementary Concept Data 2023