Hyperbilirubinemia, Hereditary
"Hyperbilirubinemia, Hereditary" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus,
MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure,
which enables searching at various levels of specificity.
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.
| Descriptor ID |
D006933
|
| MeSH Number(s) |
C16.320.565.300 C18.452.648.300
|
| Concept/Terms |
Hyperbilirubinemia, Hereditary- Hyperbilirubinemia, Hereditary
- Hereditary Hyperbilirubinemia
- Hereditary Hyperbilirubinemias
- Hyperbilirubinemias, Hereditary
Rotor Syndrome- Rotor Syndrome
- Syndrome, Rotor
- Hyperbilirubinemia, Rotor Type
- Rotor Type Hyperbilirubinemia
|
Below are MeSH descriptors whose meaning is more general than "Hyperbilirubinemia, Hereditary".
Below are MeSH descriptors whose meaning is more specific than "Hyperbilirubinemia, Hereditary".
This graph shows the total number of publications written about "Hyperbilirubinemia, Hereditary" by people in this website by year, and whether "Hyperbilirubinemia, Hereditary" was a major or minor topic of these publications.
![]()
To see the data from this visualization as text,
click here.
Below are the most recent publications written about "Hyperbilirubinemia, Hereditary" by people in Profiles.
-
Excess lipofuscin accumulation in constitutional hepatic dysfunction (Gilbert's syndrome). Light and electron microscopic observations. Arch Pathol. 1971 Jan; 91(1):41-7.
-
Formation, transport, metabolism and excretion of bilirubin. N Engl J Med. 1969 Jun 12; 280(24):1339-45.
-
Chronic nonhemolytic unconjugated hyperbilirubinemia with glucuronyl transferase deficiency: evidence for genetic heterogeneity. Trans Assoc Am Physicians. 1968; 81:66-75.