Crigler-Najjar Syndrome [Criglerův-Najjarův syndrom]
- Terms
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Criglerův-Najjarův syndrom 1. typu
Criglerův-Najjarův syndrom typu I
dědičná nehemolytická hyperbilirubinemie
familiární nehemolytická hyperbilirubinemie
kongenitální nehemolytická hyperbilirubinemie
syndrom Criglerův-Najjarův
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Crigler Najjar Syndrome
Crigler Najjar Syndrome, Type 1
Crigler-Najar Syndrome
Crigler-Najjar Syndrome, Type I
Familial Nonhemolytic Unconjugated Hyperbilirubinemia
Hereditary Unconjugated Hyperbilirubinemia
A familial form of congenital hyperbilirubinemia transmitted as an autosomal recessive trait. It is characterized by icterus and brain damage caused by a glucuronyl transferase deficiency in the liver and faulty bilirubin conjugation.
- DUI
- D003414 MeSH Browser
- CUI
- M0005322
- History note
- 91(75); was see under HYPERBILIRUBINEMIA, HEREDITARY 1975-90
- Online note
- use HYPERBILIRUBINEMIA, HEREDITARY to search CRIGLER-NAJJAR SYNDROME 1966-74
- Public note
- 91; was see under HYPERBILIRUBINEMIA, HEREDITARY 1975-90
Allowable subheadings
- BL
- blood
- CF
- cerebrospinal fluid
- CI
- chemically induced
- CL
- classification 2
- CO
- complications
- DI
- diagnosis 8
- DG
- diagnostic imaging
- DH
- diet therapy
- DT
- drug therapy
- EC
- economics
- EM
- embryology
- EN
- enzymology
- EP
- epidemiology
- EH
- ethnology
- ET
- etiology 2
- GE
- genetics 7
- HI
- history
- IM
- immunology
- ME
- metabolism 3
- MI
- microbiology
- MO
- mortality
- NU
- nursing
- PS
- parasitology
- PA
- pathology 1
- PP
- physiopathology 2
- PC
- prevention & control
- PX
- psychology
- RT
- radiotherapy
- RH
- rehabilitation
- SU
- surgery
- TH
- therapy 7
- UR
- urine
- VE
- veterinary
- VI
- virology
Crigler Najjar syndrome, type 2 Disease MeSH Browser