Medical Subject Headings

Last uploaded: November 5, 2019
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Preferred Name

Crigler-Najjar Syndrome
Synonyms

Crigler Najjar Syndrome, Type I
Definitions

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.
ID

http://purl.bioontology.org/ontology/MESH/D003414
altLabel

Crigler Najjar Syndrome, Type I

Familial Nonhemolytic Unconjugated Hyperbilirubinemia

Crigler-Najjar Syndrome, Type I

Crigler-Najar Syndrome

Crigler Najjar Syndrome

Crigler Najar Syndrome

Hereditary Unconjugated Hyperbilirubinemia

Crigler Najjar Syndrome, Type 1
AQL

BL CF CI CL CO DG DH DI DT EC EH EM EN EP ET GE HI IM ME MI MO NU PA PC PP PS PX RH RT SU TH UR VE VI
cui

C0010324
DC

1
definition

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.
DX

19910101
HN

91(75); was see under HYPERBILIRUBINEMIA, HEREDITARY 1975-90
Inverse of AQ

http://purl.bioontology.org/ontology/MESH/Q000401

http://purl.bioontology.org/ontology/MESH/Q000150

http://purl.bioontology.org/ontology/MESH/Q000188

http://purl.bioontology.org/ontology/MESH/Q000517

http://purl.bioontology.org/ontology/MESH/Q000201

http://purl.bioontology.org/ontology/MESH/Q000145

http://purl.bioontology.org/ontology/MESH/Q000503

http://purl.bioontology.org/ontology/MESH/Q000453

http://purl.bioontology.org/ontology/MESH/Q000208

http://purl.bioontology.org/ontology/MESH/Q000134

http://purl.bioontology.org/ontology/MESH/Q000821

http://purl.bioontology.org/ontology/MESH/Q000382

http://purl.bioontology.org/ontology/MESH/Q000601

http://purl.bioontology.org/ontology/MESH/Q000235

http://purl.bioontology.org/ontology/MESH/Q000523

http://purl.bioontology.org/ontology/MESH/Q000276

http://purl.bioontology.org/ontology/MESH/Q000191

http://purl.bioontology.org/ontology/MESH/Q000652

http://purl.bioontology.org/ontology/MESH/Q000662

http://purl.bioontology.org/ontology/MESH/Q000628

http://purl.bioontology.org/ontology/MESH/Q000196

http://purl.bioontology.org/ontology/MESH/Q000534

http://purl.bioontology.org/ontology/MESH/Q000266

http://purl.bioontology.org/ontology/MESH/Q000532

http://purl.bioontology.org/ontology/MESH/Q000139

http://purl.bioontology.org/ontology/MESH/Q000378

http://purl.bioontology.org/ontology/MESH/Q000175

http://purl.bioontology.org/ontology/MESH/Q000000981

http://purl.bioontology.org/ontology/MESH/Q000097

http://purl.bioontology.org/ontology/MESH/Q000473

http://purl.bioontology.org/ontology/MESH/Q000451

http://purl.bioontology.org/ontology/MESH/Q000209

http://purl.bioontology.org/ontology/MESH/Q000178

http://purl.bioontology.org/ontology/MESH/Q000469
Inverse of SIB

http://purl.bioontology.org/ontology/MESH/D007566

http://purl.bioontology.org/ontology/MESH/D005878
Machine permutation

91; was see under HYPERBILIRUBINEMIA, HEREDITARY 1975-90
Mapped from

http://purl.bioontology.org/ontology/MESH/C536213
MDA

19990101
MMR

20130708
MN

C16.320.565.300.281

C18.452.648.300.281
notation

D003414
OL

use HYPERBILIRUBINEMIA, HEREDITARY to search CRIGLER-NAJJAR SYNDROME 1966-74
prefLabel

Crigler-Najjar Syndrome
TERMUI

T839574

T009939

T811473

T841217

T841216

T841215

T009940
TH

NLM (1975)

UNK (19XX)

NLM (2014)

ORD (2010)

OMIM (2013)

GHR (2014)
tui

T047
subClassOf

http://purl.bioontology.org/ontology/MESH/D006933
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