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Hyperbilirubinemia, Hereditary MeSH Descriptor Data 2026


MeSH Heading
Hyperbilirubinemia, Hereditary
Tree Number(s)
C16.320.565.300
C18.452.648.300
Unique ID
D006933
RDF Unique Identifier
http://id.nlm.nih.gov/mesh/D006933
Annotation
do not use /‌congen & do not coord with INFANT, NEWBORN, DISEASES
Scope Note
Inborn errors of bilirubin metabolism resulting in excessive amounts of bilirubin in the circulating blood, either because of increased bilirubin production or because of delayed clearance of bilirubin from the blood.
Entry Term(s)
Hyperbilirubinemia, Rotor Type
Rotor Syndrome
NLM Classification #
QU 265
Public MeSH Note
65
History Note
65
Date Introduced
1965/01/01
Last Updated
2012/07/03
Hyperbilirubinemia, Hereditary Preferred
Rotor Syndrome Narrower
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