| 疾病名称 |
别名 |
|
| Hyperbilirubinemia, Rotor Type |
|
Rotor Syndrome
|
HBLRR
|
|
Rotor-Type Hyperbilirubinemia
|
Hyperbilirubinemia, Rotor Type, Digenic
|
|
|
| Gilbert Syndrome |
|
Gilbert Disease
|
Gilbert'S Disease
|
|
Gilbert'S Syndrome
|
Cholemia, Familial
|
|
Familial Nonhemolytic Jaundice
|
Meulengracht Syndrome
|
|
Gilbert Syndrome, Susceptibility To
|
Hyperbilirubinemia, Gilbert Type
|
|
Hblrg
|
Hyperbilirubinemia, Arias Type
|
|
Hyperbilirubinemia I
|
Constitutional Hyperbilirubinemia
|
|
Gilbert-Meulengracht Syndrome
|
Hereditary Nonhemolytic Jaundice
|
|
Hyperbilirubinemia Arias Type
|
Hyperbilirubinemia Type 1
|
|
Constitutional Liver Dysfunction
|
Gilbert-Lereboullet Syndrome
|
|
Hyperbilirubinemia 1
|
Unconjugated Benign Bilirubinemia
|
|
GILBS
|
Gilberts Syndrome
|
|
Familial Nonhaemolytic Jaundice
|
Constitutional Hyperbilirubinaemia
|
|
Hereditary Nonhaemolytic Bilirubinaemia
|
Familial Nonhaemolytic Bilirubinaemia
|
|
Idiopathic Hyperbilirubinaemia
|
Icterus Intermittens Juvenilis
|
|
Chronic Intermittent Juvenile Jaundice
|
Low-Grade Chronic Hyperbilirubinaemia Syndrome
|
|
Benign Unconjugated Bilirubinaemia Syndrome
|
Hereditary Nonhaemolytic Jaundice
|
|
Idiopathic Unconjugated Hyperbilirubinaemia
|
Gilbert--Lereboullet Syndrome
|
|
Constitutional Hepatic Dysfunction
|
Meulengracht Icterus
|
|
Cholaemia Familiaris Simplex
|
Familial Cholaemia
|
|
Congenital Familial Cholaemia
|
Physiologic Cholaemia
|
|
Hyperbilirubinaemia Type 1
|
Gilbert Cholaemia
|
|
|
| Neonatal Jaundice |
|
Neonatal Hyperbilirubinemia
|
Neonatal Icterus
|
|
Jaundice Neonatal
|
Jaundice, Neonatal
|
|
Hyperbilirubinemia, Neonatal
|
|
|
| Bilirubin Metabolic Disorder |
|
Hyperbilirubinemia
|
Hereditary Hyperbilirubinemia
|
|
Hyperbilirubinemia, Hereditary
|
Hyperbilirubinaemia
|
|
|
| Cholestasis |
|
Obstruction Of Bile Duct
|
Bile Duct Obstruction
|
|
Bile Occlusion
|
Extrahepatic Biliary Obstruction
|
|
Extrahepatic Bile Duct Obstruction
|
Bile Stasis
|
|
Biliary Stasis
|
Obstructive Hyperbilirubinemia
|
|
Obstructed Jaundice
|
Bile Duct Obstructed
|
|
Bile Ductal Obstruction
|
Biliary Duct Obstruction
|
|
Obstructed Bile Ductal
|
Obstructed Biliary Duct
|
|
Obstructed Biliary Ductal
|
Jaundice Regurgitation
|
|
Obstructive Jaundice
|
Cholestatic Jaundice
|
|
Cholestatic Jaundice Syndrome
|
|
|
| Glucosephosphate Dehydrogenase Deficiency |
|
G6pd Deficiency
|
Glucose-6-Phosphate Dehydrogenase Deficiency
|
|
Deficiency Of Glucose-6-Phosphate Dehydrogenase
|
Glucose 6 Phosphate Dehydrogenase Deficiency
|
|
Deficiency Of G-6pd
|
G6pdd
|
|
|
| Coumarin Resistance |
|
Warfarin Resistance
|
Warfarin Sensitivity
|
|
Coumadin Sensitivity
|
Warfarin Response
|
|
Poor Metabolism Of Coumarin
|
Coumarin, Poor Metabolism Of
|
|
CMRES
|
|
|
| Intrahepatic Cholestasis |
|
Cholestasis, Intrahepatic
|
Neonatal Intrahepatic Cholestasis
|
|
Cholestasis Intrahepatic
|
Cholestasis Of Pregnancy
|
|
|
| Dubin-Johnson Syndrome |
|
DJS
|
Chronic Idiopathic Jaundice
|
|
Jaundice, Chronic Idiopathic
|
Hyperbilirubinemia, Dubin-Johnson Type
|
|
Hyperbilirubinemia Ii
|
Hyperbilirubinemia Type 2
|
|
Conjugated Hyperbilirubinemia
|
Dubin-Sprinz Disease
|
|
Sprinz-Nelson Syndrome
|
Hblrdj
|
|
Dubin Johnson Syndrome
|
Hyperbilirubinemia 2
|
|
Black Liver-Jaundice Syndrome
|
Chronic Idiopathic Jaundice With Pigmented Liver
|
|
Dubin-Sprinz Syndrome
|
Hyperbilirubinaemia Type 2
|
|
Djs - [Dubin-Johnson Syndrome]
|
|
|
| Cholestasis, Benign Recurrent Intrahepatic, 1 |
|
Benign Recurrent Intrahepatic Cholestasis
|
BRIC1
|
|
Summerskill Syndrome
|
Bric
|
|
Summerskill-Walshe-Tygstrup Syndrome
|
Cholestasis, Benign Recurrent Intrahepatic
|
|
Benign Recurrent Intrahepatic Cholestasis 1
|
Benign Recurrent Intrahepatic Cholestasis Type 1
|
|
Bric Type 1
|
Low Gamma-Gt Familial Intrahepatic Cholestasis
|
|
Recurrent Familial Intrahepatic Cholestasis
|
Cholestasis, Benign Recurrent Intrahepatic 1
|
|
Mild Atp8b1 Deficiency
|
Recurrent Familial Intrahepatic Cholestasis 1
|
|
Abcb11-Related Intrahepatic Cholestasis
|
Atp8b1-Related Intrahepatic Cholestasis
|
|
Cholestasis, Intrahepatic, Recurrent, Benign, Type 1
|
Progressive Intrahepatic Cholestasis
|
|
Cholestasis, Progressive Familial Intrahepatic 3
|
Bric - [Benign Recurrent Intrahepatic Cholestasis]
|
|
|
| Liver Lipoma |
|
Hepatic Lipoma
|
Lipoma Of The Liver
|
|
|
| Carbapenem Allergy |
|
|
| Myopathy |
|
Muscular Diseases
|
Myopathies
|
|
|
| Liver Disease |
|
Liver Failure
|
Liver Diseases
|
|
Abnormality Of The Liver
|
Liver Dysfunction
|
|
Disorder Of Liver
|
Hepatic Disorder
|
|
Hepatic Disease
|
Disease Of Bilirubin Metabolism
|
|
Disorder Of Bilirubin Metabolism
|
Liver Decompensation
|
|
Liver Function Failure
|
Hepatic Failure Nos
|
|
Liver Failure Nos
|
End Stage Liver Disease
|
|
Decompensated Liver Failure
|
Decompensation Of Liver Function
|
|
Hepatic Decompensation
|
Hepatic Insufficiency
|
|
Liver Cell Necrosis With Hepatic Failure
|
Liver Insufficiency
|
|
Decompensated Liver Disease
|
End Stage Liver Failure
|
|
Liver Necrosis With Hepatic Failure
|
|
|
| Thiopurines, Poor Metabolism Of, 1 |
|
Thiopurine S-Methyltransferase Deficiency
|
Tpmt Deficiency
|
|
Thiopurine Methyltransferase Deficiency
|
Thiopurine S Methyltranferase Deficiency
|
|
THPM1
|
Tpmtd
|
|
Poor Metabolism Of Thiopurines-1
|
6-Mercaptopurine Sensitivity
|
|
Thiopurines, Poor Metabolism Of
|
Poor Metabolism Of Thiopurines
|
|
|
| Abacavir Allergy |
|
|
| Neutropenia |
|
|
| Primary Biliary Cholangitis |
|
Primary Biliary Cirrhosis
|
Biliary Liver Cirrhosis
|
|
Chronic Nonsuppurative Destructive Cholangitis
|
Familial Primary Biliary Cirrhosis
|
|
Pbc
|
Hanot Syndrome
|
|
Cholestatic Cirrhosis
|
Biliary Cirrhosis Primary
|
|
Liver Cirrhosis, Biliary
|
Hanot'S Cirrhosis
|
|
Biliary Cirrhosis
|
Pericholangiolic Biliary Cirrhosis
|
|
Tannhauser-Magendantz Syndrome
|
Hanot-Rossle Syndrome
|
|
Hypertrophic Cirrhosis
|
Todd Cirrhosis
|
|
Hanot Cirrhosis
|
Charcot Cirrhosis
|
|
Mahon-Tannhauser Syndrome
|
Toxic Cirrhosis
|
|
Hypertrophic Biliary Cirrhosis
|
Monolobular Cirrhosis
|
|
Unilobar Cirrhosis
|
Xanthomatous Biliary Cirrhosis
|
|
|
| Pigmentation Disease |
|
Pigmentation Disorders
|
Skin Pigmentation Disorder
|
|
|
| Crigler-Najjar Syndrome, Type I |
|
Crigler-Najjar Syndrome
|
Crigler-Najjar Syndrome Type 1
|
|
Bilirubin Udp Glucuronyl Transferase Deficiency
|
Crigler Najjar Syndrome
|
|
Crigler Najjar Syndrome, Type 1
|
Bilirubin Uridinediphosphate Glucuronosyltransferase Deficiency
|
|
Bilirubin-Ugt Deficiency
|
Hyperbilirubinemia, Crigler-Najjar Type I
|
|
Hblrcn1
|
Familial Nonhemolytic Unconjugated Hyperbilirubinemia
|
|
Hereditary Unconjugated Hyperbilirubinemia
|
Bilirubin Uridinediphosphate Glucuronosyltransferase Deficiency Type 1
|
|
Bilirubin-Ugt Deficiency Type 1
|
Crigler-Najjar Syndrome 1
|
|
CN1
|
Cn-I
|
|
Crigler-Najjar Syndrome Type I
|
Hereditary Unconjugated Hyperbilirubinaemia
|
|
Ugt Deficiency
|
Bilirubin Glucuronosyltransferase Deficiency
|
|
Crigler-Najjar Disease Or Syndrome
|
Deficiency Of Glucuronosyltransferase
|
|
Glucuronyl Transferase Deficiency
|
Glucuronyltransferase Deficiency
|
|
Udp Glucuronyl Transferase Deficiency
|
Cns - [Crigler-Najjar Syndrome]
|
|
Congenital Familial Nonhemolytic Jaundice
|
|
|
| Intrahepatic Cholestasis Of Pregnancy |
|
Recurrent Intrahepatic Cholestasis Of Pregnancy
|
Gravidic Intrahepatic Cholestasis
|
|
Pregnancy-Related Cholestasis
|
Icp
|
|
Pregnancy Related Cholestasis
|
Cholestasis, Intrahepatic Of Pregnancy
|
|
Familial Intrahepatic Cholestasis Of Pregnancy
|
Familial Recurrent Intrahepatic Cholestasis Of Pregnancy
|
|
Ricp
|
Obstetric Cholestasis
|
|
|
| Progressive Familial Intrahepatic Cholestasis |
|
Abcb4-Related Intrahepatic Cholestasis
|
Cholestasis, Progressive Familial Intrahepatic
|
|
Pfic
|
Byler Disease
|
|
Abcb11-Related Intrahepatic Cholestasis
|
Atp8b1-Related Intrahepatic Cholestasis
|
|
Bsep Deficiency
|
Byler Disease
|
|
Byler Syndrome
|
Fic1 Deficiency
|
|
Low Γ-Gt Familial Intrahepatic Cholestasis
|
Mdr3 Deficiency
|
|
Pfic
|
Cholestasis, Intrahepatic, Familial, Progressive
|
|
Pfic - [Progressive Familial Intrahepatic Cholestasis]
|
|
|
| Muscle Tissue Disease |
|
|
| Severe Cutaneous Adverse Reaction |
|
Stevens-Johnson Syndrome
|
Toxic Epidermal Necrolysis
|
|
Drug-Induced Stevens Johnson Syndrome
|
Stevens-Johnson Syndrome Toxic Epidermal Necrolysis Spectrum
|
|
Susceptibility To Severe Cutaneous Adverse Reaction
|
Stevens-Johnson Syndrome/Toxic Epidermal Necrolysis
|
|
Lyell'S Syndrome
|
Lyell Syndrome
|
|
Severe Cutaneous Adverse Reaction, Susceptibility To
|
Hypersensitivity Syndrome, Carbamazepine-Induced, Susceptibility To
|
|
Hypersensitivity Syndrome, Carbamazepine-Induced
|
Stevens-Johnson Syndrome, Susceptibility To
|
|
Toxic Epidermal Necrolysis, Susceptibility To
|
Sjs/Ten
|
|
Susceptibility To Severe Cutaneous Adverse Reaction Ity To
|
Mycoplasma-Induced Stevens Johnson Syndrome
|
|
Dermatostomatitis, Stevens Johnson Type
|
Stevens-Johnson Syndrome/Toxic Epidermal Necrolysis Spectrum
|
|
Sjs-Ten
|
Toxic Epidermolysis
|
|
SJS
|
Dermatostomatitis Stevens Johnson Type
|
|
Ten
|
Sjs/Ten - [Stevens-Johnson Syndrome And Toxic Epidermal Necrolysis]
|
|
Ten - [Toxic Epidermal Necrolysis]
|
|
|
