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Hyperbilirubinemia, Hereditary MeSH Descriptor Data 2021


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
Public MeSH Note
65
History Note
65
Date Established
1965/01/01
Date of Entry
1999/01/01
Revision Date
2012/07/03
Hyperbilirubinemia, Hereditary Preferred
Rotor Syndrome Narrower
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