| Diseases |
Alias |
|
| 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
|
|
|
| Crigler-Najjar Syndrome, Type Ii |
|
Crigler-Najjar Syndrome Type 2
|
Hyperbilirubinemia, Crigler-Najjar Type Ii
|
|
Hblrcn2
|
Arias Syndrome
|
|
Crigler Najjar Syndrome Type 2
|
Bilirubin Uridinediphosphate Glucuronosyltransferase Deficiency Type 2
|
|
Bilirubin-Ugt Deficiency Type 2
|
Crigler-Najjar Syndrome 2
|
|
CN2
|
Cn-Ii
|
|
Crigler-Najjar Syndrome Type Ii
|
Crigler Najjar Syndrome, Type 2
|
|
|
| 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
|
|
|
| Hyperbilirubinemia, Transient Familial Neonatal |
|
Lucey-Driscoll Syndrome
|
Transient Familial Neonatal Hyperbilirubinemia
|
|
HBLRTFN
|
Hyperbilirubinemia, Familial Transient Neonatal
|
|
Hyperbilirubinemia Transient Familial Neonatal
|
Transient Familial Hyperbilirubinemia
|
|
|
| Bilirubin, Serum Level Of, Quantitative Trait Locus 1 |
|
Bilirubin, Serum Level Of, Qtl1
|
BILIQTL1
|
|
Bilirubin, Serum Level Of, Quantitative Trait Locus, Type 1
|
|
|
| Bilirubin Metabolic Disorder |
|
Hyperbilirubinemia
|
Hereditary Hyperbilirubinemia
|
|
Hyperbilirubinemia, Hereditary
|
Hyperbilirubinaemia
|
|
|
| Kernicterus |
|
Bilirubin Encephalopathy
|
Hyperbilirubinemic Encephalopathy
|
|
Kernicterus Spectrum Disorder
|
|
|
| Neonatal Jaundice |
|
Neonatal Hyperbilirubinemia
|
Neonatal Icterus
|
|
Jaundice Neonatal
|
Jaundice, Neonatal
|
|
Hyperbilirubinemia, Neonatal
|
|
|
| Cholelithiasis |
|
|
| Cardiomyopathy, Dilated, With Hypergonadotropic Hypogonadism |
|
Malouf Syndrome
|
Najjar Syndrome
|
|
Dilated Cardiomyopathy-Hypergonadotropic Hypogonadism Syndrome
|
Cardiogenital Syndrome
|
|
Genital Anomaly With Cardiomyopathy
|
Cardiomyopathy With Primary Testicular Failure
|
|
Dilated Cardiomyopathy With Hypergonadotropic Hypogonadism
|
Cardiomyopathy, Congestive, With Hypergonadotropic Hypogonadism
|
|
Cardiomyopathy, Dilated, With Premature Ovarian Failure
|
Cardiomyopathy Eith Primary Testicular Failure
|
|
Congestive Cardiomyopathy With Hypergonadotropic Hypogonadism
|
Dilated Cardiomyopathy With Premature Ovarian Failure
|
|
CMDHH
|
Cardiomyopathy Congestive With Hypergonadotropic Hypogonadism
|
|
Cardiomyopathy Dilated With Premature Ovarian Failure
|
|
|
| Neutropenia |
|
|
| Hereditary Spherocytosis |
|
Congenital Spherocytic Hemolytic Anemia
|
Spherocytic Anemia
|
|
Congenital Spherocytosis
|
Spherocytosis, Type 1
|
|
Minkowski Chauffard Syndrome
|
Hs
|
|
Minkowski-Chauffard Disease
|
Minkowski-Chauffard Syndrome
|
|
Spherocytosis Hereditary
|
Spherocytosis, Hereditary
|
|
Anemia, Hereditary Spherocytic Hemolytic
|
|
|
| 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
|
|
|
| Choledocholithiasis |
|
|
| Thalassemia |
|
Sickle-Cell Thalassemia With Crisis
|
Sickle-Cell Thalassemia Without Crisis
|
|
Thalassemia Hb-S Disease With Crisis
|
Thalassemia Hb-S Disease Without Crisis
|
|
Thalassemias
|
Hereditary Leptocytosis
|
|
Haemoglobin Thalassaemia Disorder
|
Thalassaemia Syndrome
|
|
Thalassaemia Nos
|
Thalassemia Variants
|
|
|
| Alpha-Thalassemia |
|
Alpha Thalassemia
|
Alpha Thalassaemia
|
|
Alpha Plus Thalassemia
|
Thalassemia, Alpha-
|
|
Thalassemias, Alpha-
|
A-Thalassemia
|
|
Α-Thalassemia
|
A-THAL
|
|
Thalassemia
|
Alpha Thalassaemia Syndrome
|
|
|
| Beta-Thalassemia |
|
Beta Thalassemia
|
Cooley'S Anemia
|
|
Mediterranean Anemia
|
Beta Thalassemia Intermedia
|
|
Erythroblastic Anemia
|
Thalassemia, Hispanic Gamma-Delta-Beta
|
|
Thalassemia Major
|
Thalassemia Minor
|
|
Beta-Plus-Thalassemia
|
Thalassemia, Beta
|
|
Beta Thalassemia Major
|
Beta Thalassemia Minor
|
|
Thalassemias, Beta-
|
Microcytemia, Beta Type
|
|
Thalassemia, Beta Type
|
B-THAL
|
|
Mediterranean Anaemia
|
Beta Thalassaemia Syndrome
|
|
Mediterranean Disease
|
Beta Thalassaemia Disease
|
|
|
| Pigmentation Disease |
|
Pigmentation Disorders
|
Skin Pigmentation Disorder
|
|
|
| Sickle Cell Disease |
|
Hbs Disease
|
Hemoglobin S Disease
|
|
Scd
|
Sickle Cell Disorders
|
|
Sickling Disorder Due To Hemoglobin S
|
Anemia, Sickle Cell
|
|
Hb-Ss Disease Without Crisis
|
Hbss Without Crisis
|
|
Sickle-Cell Anaemia Without Crisis
|
Scd - [Sickle Cell Disease]
|
|
Sca - [Sickle Cell Anaemia]
|
Sickle Cell Disease Nos
|
|
Sickle Cell Disorder
|
Sickle Cell Syndrome
|
|
Sickle-Cell Anaemia Nos
|
Sickle-Cell Disorder Nos
|
|
Haemoglobin S Disease
|
Haemoglobin Ss Disease
|
|
Hb S Disease
|
Hb Ss Disease
|
|
Herrick Anaemia
|
Hereditary Haemoglobinopathy Disorder Homozygous For Haemoglobin S
|
|
Sickle-Cell Haemoglobin Disease
|
Sickling Disorder Due To Haemoglobin S
|
|
Hb-Ss Disease With Crisis
|
Sickle Cell Crisis
|
|
Sickle-Cell Disorder With Crisis
|
Sickle-Cell Anaemia With Crisis
|
|
Hbss With Crisis
|
Hb S Disease With Mention Of Crisis
|
|
Haemoglobin Ss Disease With Crisis
|
Hb-Ss Disease With Vaso-Occlusive Pain
|
|
Vaso-Occlusive Crisis
|
|
|
| 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
|
|
|
| Diarrhea |
|
Diarrhoea
|
Diarrhea Of Presumed Infectious Origin
|
|
|
| Hemolytic Anemia |
|
Anemia, Hemolytic
|
Anemia Hemolytic
|
|
Anaemia Due To Other Disorders Of Glutathione Metabolism
|
Chronic Non Spherocytic Anaemia
|
|
G6pd - [Glucose-6-Phosphate Dehydrogenase Deficiency] Anaemia
|
Anaemia Due To Glucose-6-Phosphate Dehydrogenase Deficiency
|
|
Glucose-6-Phosphate Dehydrogenase Deficiency With Anaemia
|
Glucose-6-Phosphate Dehydrogenase Deficiency Anaemia
|
|
Favism Anaemia
|
Haemolytic Anaemia Due Tog6pd Deficiency
|
|
Favism
|
Pentose Phosphate Pathway Disorder Anaemia
|
|
Anaemia Due To Pentose Phosphate Pathway Defect
|
|
|
| Autoimmune Hepatitis |
|
Aih
|
Hepatitis, Autoimmune
|
|
Autoimmune Chronic Active Hepatitis
|
Autoimmune Hepatitis With Centrilobular Necrosis
|
|
Autoimmune Chronic Hepatitis
|
Hepatitis Autoimmune
|
|
|
| Epicardium Cancer |
|
Malignant Neoplasm Of Epicardium
|
Epicardial Tumor
|
|
Malignant Epicardial Tumor
|
Neoplasm Of Epicardium
|
|
|
| Colorectal Cancer |
|
Colon Cancer
|
Colorectal Carcinoma
|
|
Colon Carcinoma
|
Colorectal Cancer, Susceptibility To
|
|
Carcinoma Of Colon
|
CRC
|
|
Colorectal Cancer With Chromosomal Instability, Somatic
|
Colon Cancer, Somatic
|
|
Colon Cancer, Susceptibility To
|
Colonic Neoplasms
|
|
Colorectal Neoplasms
|
Colorectal Cancer, Somatic
|
|
Colon Cancer, Advanced, Somatic
|
Colonic Carcinoma
|
|
Colorectal Carcinomas
|
Colon Cancers
|
|
Colorectal Cancers
|
Cancer, Colorectal, Somatic
|
|
Cancer, Colon
|
Cancer, Colorectal, Susceptibility To
|
|
Colorectal Neoplasm
|
Colonic Neoplasm
|
|
Malignant Tumor Of Colon
|
|
|
| Acetaminophen Metabolism |
|
|
| Dihydropyrimidine Dehydrogenase Deficiency |
|
Dpd Deficiency
|
Familial Pyrimidinemia
|
|
Hereditary Thymine-Uraciluria
|
Dihydropyrimidinuria
|
|
Dpyd Deficiency
|
Thymine-Uraciluria, Hereditary
|
|
Pyrimidinemia, Familial
|
5-Fluorouracil Toxicity
|
|
Dihydrouracil Dehydrogenase Deficiency
|
Familial Pyrimidinaemia
|
|
Thymine-Uracilurea
|
Familial Pyrimidemia
|
|
Pyrimidinemia Familial
|
DPYDD
|
|
|
| Blood Group Incompatibility |
|
|
| Coumarin Resistance |
|
Warfarin Resistance
|
Warfarin Sensitivity
|
|
Coumadin Sensitivity
|
Warfarin Response
|
|
Poor Metabolism Of Coumarin
|
Coumarin, Poor Metabolism Of
|
|
CMRES
|
|
|
| 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
|
|
|
| Nephrotic Syndrome, Type 20 |
|
NPHS20
|
Nephrotic Syndrome Type 20
|
|
Nephrotic Syndrome 20
|
|
|
| Endometrial Cancer |
|
Endometrial Carcinoma
|
Endometrial Neoplasm
|
|
Malignant Neoplasm Of Endometrium
|
Endometrioid Carcinoma
|
|
Endometrial Neoplasms
|
Carcinoma, Endometrioid
|
|
Endometrial Cancer, Familial
|
Endometrial Carcinoma, Somatic
|
|
Endometrial Cancer, Susceptibility To
|
Endometrial Ca
|
|
Malignant Endometrial Neoplasm
|
Neoplasm Of Endometrium
|
|
Primary Malignant Neoplasm Of Endometrium
|
Tumor Of Endometrium
|
|
Carcinoma Of The Endometrium
|
Endometrioid Carcinoma Of Female Reproductive System
|
|
ENDMC
|
Carcinoma Endometrioid
|
|
Endometrial Cancers
|
Cancer, Endometrial
|
|
Uterine Corpus Cancer
|
|
|
| Lung Cancer |
|
Lung Carcinoma
|
Non-Small Cell Lung Carcinoma
|
|
Lung Cancer, Susceptibility To
|
Lung Cancer, Protection Against
|
|
Adenocarcinoma Of Lung, Somatic
|
Adenocarcinoma Of Lung, Response To Tyrosine Kinase Inhibitor In
|
|
Nonsmall Cell Lung Cancer
|
Lung Neoplasm
|
|
Carcinoma Of Lung
|
Lung Non-Small Cell Carcinoma
|
|
Non-Small Cell Lung Cancer
|
Nsclc
|
|
Lung Neoplasms
|
Malignant Neoplasm Of Lung
|
|
Alveolar Cell Carcinoma
|
Nonsmall Cell Lung Cancer, Somatic
|
|
Nonsmall Cell Lung Cancer, Response To Tyrosine Kinase Inhibitor In
|
Nonsmall Cell Lung Cancer, Susceptibility To
|
|
Lung Cancer, Somatic
|
Lung Cancer, Resistance To
|
|
Cancer Of Lung
|
Cancer Of Bronchus
|
|
Cancer Of The Lung
|
Lung Malignancies
|
|
Lung Malignant Tumors
|
Malignant Lung Tumor
|
|
Malignant Tumor Of Lung
|
Pulmonary Cancer
|
|
Pulmonary Carcinoma
|
Pulmonary Neoplasms
|
|
Respiratory Carcinoma
|
LNCR
|
|
Adenocarcinoma Of Lung
|
Neoplasm Of Lung
|
|
Cancer Lung
|
Carcinoma Non-Small Cell Lung
|
|
Carcinoma, Non-Small-Cell Lung
|
Lung Cancers
|
|
Lung Carcinomas
|
Cancer, Lung
|
|
Cancer, Lung, Non-Small Cell
|
Primary Malignant Neoplasm Of Lung
|
|
Bronchioloalveolar Adenocarcinoma
|
|
|
| Autosomal Dominant Beta Thalassemia |
|
Inclusion Body Beta-Thalassemia
|
|
|
| Sickle Cell Anemia |
|
Hemoglobin Sc Disease
|
Anemia, Sickle Cell
|
|
Hbsc Disease
|
Sickle Cell-Hemoglobin C Disease Syndrome
|
|
Hb Ss Disease
|
Sickle Cell Trait
|
|
Drepanocytosis
|
Haemoglobin Sc Disease
|
|
Hb Sc Disease
|
Hb-S/Hb-C Disease
|
|
Hb-Ss Disease Without Crisis
|
Hemoglobin S Disease Without Crisis
|
|
Sickle Cell Anaemia
|
Sickle-Cell/Hb-C Disease Without Crisis
|
|
Sickle Cell - Hemoglobin C Disease
|
Hbs Disease
|
|
Hemoglobin S Disease
|
Sickling Disorder Due To Hemoglobin S
|
|
SKCA
|
Sickle Cell Disease
|
|
Sickle Cell-Hemoglobin C Disease
|
Sickle-Cell Disease Carrier
|
|
Sickle-Cell Heterozygous Disorder
|
Haemoglobin A-S Genotype
|
|
Hb-S - [Sickle Cell Haemoglobin] Carrier
|
Sickle Cell Haemoglobin Trait
|
|
As - [Sickle Cell Trait]
|
Hbas - [Sickle Cell Haemoglobin Trait]
|
|
Sickle-Cell Trait Haemoglobin Disease
|
Haemoglobin Sickle Cell Trait Disorder
|
|
Heterozygous Sickle Cell Trait
|
Hbas - [Heterozygous Haemoglobin S]
|
|
|
| Breast Cancer |
|
Breast Carcinoma
|
Male Breast Cancer
|
|
Breast Cancer, Familial
|
Malignant Neoplasm Of Breast
|
|
Breast Cancer, Susceptibility To
|
Breast Cancer, Early-Onset
|
|
Malignant Tumor Of Breast
|
Carcinoma Of Male Breast
|
|
Breast Cancer, Invasive Ductal
|
Breast Cancer, Protection Against
|
|
Breast Cancer, Somatic
|
Breast Cancer, Male
|
|
Breast Cancer, Lobular, Somatic
|
Breast Tumor
|
|
Mammary Cancer
|
Mammary Tumor
|
|
Malignant Neoplasm Of Male Breast
|
Mammary Carcinoma
|
|
Male Breast Carcinoma
|
Familial Cancer Of Breast
|
|
Invasive Ductal Breast Carcinoma
|
Breast Cancer Susceptibility
|
|
Breast Cancer, Male, Susceptibility To
|
Breast Cancer, Early-Onset, Susceptibility To
|
|
Malignant Tumor Of The Breast
|
Mammary Neoplasm
|
|
Primary Breast Cancer
|
Neoplasm Of Male Breast
|
|
Carcinoma Of Breast
|
Breast Cancer In Men
|
|
Familial Breast Cancer
|
Cancer Of Breast
|
|
BC
|
Breast Cancer Familial
|
|
Breast Cancer Familial Male
|
Breast Cancer, Familial Male
|
|
Breast Male Carcinoma
|
Breast Neoplasms
|
|
Breast Neoplasms, Male
|
Mammary Tumors
|
|
Mammary Carcinomas
|
Cancer, Breast
|
|
Cancer, Breast, Susceptibility
|
Invasive Breast Ductal Carcinoma
|
|
Breast Neoplasm
|
Susceptibility To Breast Cancer
|
|
Mammary Neoplasms
|
Animal Mammary Neoplasms
|
|
Primary Malignant Neoplasm Of Breast
|
Infiltrating Ductal Carcinoma Of Breast
|
|
Infiltrating Duct Carcinoma Of Unspecified Site
|
Infiltrating Ductular Carcinoma Of Unspecified Site
|
|
Invasive Breast Carcinoma Of No Special Type
|
Microinvasive Carcinoma Of Breast
|
|
Carcinoma With Apocrine Differentiation
|
|
|
| Autism Spectrum Disorder |
|
Asd
|
Autism Spectrum Disorders
|
|
Autistic Continuum
|
Pervasive Developmental Disorder
|
|
Pervasive Development Disorder
|
Autistic Behavior
|
|
Autistic Disorder
|
Autistic
|
|
Autistic Disorder Of Childhood Onset
|
Infantile Autism
|
|
Childhood Autism
|
Kanner Syndrome
|
|
Pervasive Developmental Delay Nos
|
Pervasive Developmental Disorder, Not Otherwise Specified
|
|
|
