Search on: FAMILIAL NONHEMOLYTIC JAUNDICE 
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Descriptor English:   Gilbert Disease 
Descriptor Spanish:   Enfermedad de Gilbert 
Descriptor Portuguese:   Doença de Gilbert 
Synonyms English:   Arias Type Hyperbilirubinemia
Arias Type Hyperbilirubinemias
Constitutional Liver Dysfunction
Disease, Gilbert
Disease, Gilbert's
Familial Nonhemolytic Jaundice
Gilbert Syndrome
Gilbert's Disease
Gilbert's Syndrome
Gilbert-Lereboullet Syndrome
Gilberts Disease
Gilberts Syndrome
Hyperbilirubinemia 1
Hyperbilirubinemia 1s
Hyperbilirubinemia I
Hyperbilirubinemia, Arias Type
Hyperbilirubinemias, Arias Type
Meulengracht Syndrome
Syndrome, Gilbert
Syndrome, Gilbert's
Unconjugated Benign Bilirubinemia  
Tree Number:   C16.320.565.300.528
C18.452.648.300.528
Definition English:   A benign familial disorder, transmitted as an autosomal dominant trait. It is characterized by low-grade chronic hyperbilirubinemia with considerable daily fluctuations of the bilirubin level. 
History Note English:   2000(1975) 
Allowable Qualifiers English:  
BL blood CF cerebrospinal fluid
CI chemically induced CL classification
CO complications DI diagnosis
DG diagnostic imaging DH diet therapy
DT drug therapy EC economics
EM embryology EN enzymology
EP epidemiology EH ethnology
ET etiology GE genetics
HI history IM immunology
ME metabolism MI microbiology
MO mortality NU nursing
PS parasitology PA pathology
PP physiopathology PC prevention & control
PX psychology RT radiotherapy
RH rehabilitation SU surgery
TH therapy UR urine
VE veterinary VI virology
Record Number:   6017 
Unique Identifier:   D005878 

Occurrence in VHL:
 

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