Hyperbilirubinemia, Hereditary [familiární hyperbilirubinemie]
- Terms
-
hyperbilirubinémie dědičná
hyperbilirubinemie Rotorova typu
hyperbilirubinémie Rotorova typu
Rotorův syndrom
-
Hyperbilirubinemia, Rotor Type
Rotor Syndrome
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.
- Annotation
- do not use /congen & do not coord with INFANT, NEWBORN, DISEASES
- DUI
- D006933 MeSH Browser
- CUI
- M0010812
- History note
- 65
- Public note
- 65
Allowable subheadings
- BL
- blood 2
- CF
- cerebrospinal fluid
- CI
- chemically induced
- CL
- classification 3
- CO
- complications 2
- DI
- diagnosis 15
- DG
- diagnostic imaging
- DH
- diet therapy
- DT
- drug therapy 2
- EC
- economics
- EM
- embryology
- EN
- enzymology
- EP
- epidemiology
- EH
- ethnology
- ET
- etiology 7
- GE
- genetics 16
- HI
- history
- IM
- immunology
- ME
- metabolism 2
- MI
- microbiology
- MO
- mortality
- NU
- nursing
- PS
- parasitology
- PA
- pathology 3
- PP
- physiopathology 2
- PC
- prevention & control
- PX
- psychology
- RT
- radiotherapy
- RH
- rehabilitation
- SU
- surgery
- TH
- therapy 2
- UR
- urine 1
- VE
- veterinary
- VI
- virology
Hyperbilirubinemia, Conjugated, Type III Disease MeSH Browser
Hyperbilirubinemia, Shunt Disease MeSH Browser
Hyperbilirubinemia, Transient Familial Neonatal Disease MeSH Browser