Medical Subject Headings

Last uploaded: November 5, 2019
Preferred Name

Hyperbilirubinemia, Hereditary

Synonyms

Rotor Type Hyperbilirubinemia

Definitions

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.

ID

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

altLabel

Rotor Type Hyperbilirubinemia

Hereditary Hyperbilirubinemia

Syndrome, Rotor

Hyperbilirubinemia, Rotor Type

Hyperbilirubinemias, Hereditary

Hereditary Hyperbilirubinemias

Rotor Syndrome

AN

do not use /congen & do not coord with INFANT, NEWBORN, DISEASES

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

C0220991

C0020435

DC

1

definition

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.

DX

19650101

HN

65

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/D011371

http://purl.bioontology.org/ontology/MESH/D016464

http://purl.bioontology.org/ontology/MESH/D002239

http://purl.bioontology.org/ontology/MESH/D015499

http://purl.bioontology.org/ontology/MESH/D020157

http://purl.bioontology.org/ontology/MESH/D011686

http://purl.bioontology.org/ontology/MESH/D008664

http://purl.bioontology.org/ontology/MESH/D028226

http://purl.bioontology.org/ontology/MESH/D043202

http://purl.bioontology.org/ontology/MESH/D020739

http://purl.bioontology.org/ontology/MESH/D030401

http://purl.bioontology.org/ontology/MESH/D000592

http://purl.bioontology.org/ontology/MESH/D008052

http://purl.bioontology.org/ontology/MESH/D018901

Machine permutation

65

Mapped from

http://purl.bioontology.org/ontology/MESH/C562692

http://purl.bioontology.org/ontology/MESH/C562451

http://purl.bioontology.org/ontology/MESH/C562885

MDA

19990101

MMR

20120703

MN

C18.452.648.300

C16.320.565.300

notation

D006933

prefLabel

Hyperbilirubinemia, Hereditary

TERMUI

T020851

T020852

T753435

TH

NLM (1998)

NLM (1965)

NLM (2010)

ORD (2010)

OMIM (2013)

tui

T047

subClassOf

http://purl.bioontology.org/ontology/MESH/D008661

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http://purl.bioontology.org/ontology/ICD10CM/E80.6 International Classification of Diseases, Version 10 - Clinical Modification CUI
http://purl.bioontology.org/ontology/OMIM/237450 Online Mendelian Inheritance in Man CUI