疾病名称 |
别名 |
|
Glycogen Storage Disease Ia |
Von Gierke Disease
|
Glycogen Storage Disease Type I
|
Glycogen Storage Disease I
|
Hepatorenal Form Of Glycogen Storage Disease
|
Hepatorenal Glycogenosis
|
Glucose-6-Phosphatase Deficiency
|
Glycogen Storage Disease, Type I
|
Glycogen Storage Disease Due To Glucose-6-Phosphatase Deficiency Type Ia
|
GSD1A
|
Gsd1
|
Von Gierke'S Disease
|
Glycogen Storage Disease Type 1a
|
Glycogen Storage Disease 1a
|
Glucose-6-Phosphate Transport Defect
|
Gsd Ia
|
Deficiency Of Glucose-6-Phosphatase
|
Glycogenosis Type I
|
Glucose-6-Phosphatase Deficiency Glycogen Storage Disease
|
Glycogenosis Type 1
|
Glucose-6-Phosphate Deficiency
|
Gsd I
|
Gsd Type I
|
G6p Deficiency Type 1a
|
Gsd Due To G6p Deficiency Type 1a
|
Gsd Due To G6p Deficiency Type Ia
|
Gsd Type 1a
|
Gsdia
|
Glycogen Storage Disease Due To G6p Deficiency Type Ia
|
Glycogenosis Due To Glucose-6-Phosphatase Deficiency Type 1a
|
Glycogenosis Due To Glucose-6-Phosphatase Deficiency Type Ia
|
Glycogenosis Type Ia
|
Gsd-Ia
|
Storage Disease, Glycogen, Type 1a
|
Glycogen Storage Disease Type Ia
|
|
|
Glycogen Storage Disease |
Glycogenosis
|
Glycogenoses
|
Gsd
|
Storage Disease, Glycogen
|
Gsd - [Glycogen Storage Disease]
|
Glycogen Thesaurismosis
|
Diffuse Glycogenosis
|
Generalised Glycogen Storage Disease
|
Generalised Glycogenosis
|
Generalised Glycogen Storage Disease Of Infants
|
Glycogen Synthase Deficiency
|
|
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Hypoglycemia |
Hypoglycaemia
|
Low Blood Sugar
|
Hypoglycaemia Nos
|
Spontaneous Hypoglycaemia
|
Nondiabetic Hypoglycaemia
|
Hypoglycaemic Disorder Nos
|
Hypoglycaemic Syndrome
|
|
|
Hyperuricemia |
Blood Urate Raized
|
Uricacidemia
|
|
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Hepatocellular Adenoma |
|
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Glycogen Storage Disease Vi |
Glycogen Storage Disease Type Vi
|
Hers Disease
|
GSD6
|
Gsd Vi
|
Hepatic Glycogen Phosphorylase Deficiency
|
Phosphorylase Deficiency Glycogen-Storage Disease Of Liver
|
Hers' Disease
|
Glycogen Storage Disease Type 6
|
Glycogen Storage Disease 6
|
Gsd Type Vi
|
Glycogenosis Type Vi
|
Glycogen Storage Disease, Type Vi
|
Hepatophosphorylase Deficiency Glycogenosis
|
Liver Phosphorylase Deficiency Syndrome
|
Glycogen Storage Disease Due To Liver Glycogen Phosphorylase Deficiency
|
Gsd Due To Liver Glycogen Phosphorylase Deficiency
|
Gsd Type 6
|
Glycogenosis Due To Liver Glycogen Phosphorylase Deficiency
|
Glycogenosis Type 6
|
Hepatic Phosphorylase Deficiency
|
Liver Glycogen Phosphorylase Deficiency
|
Her
|
Glycogen Storage Disease Vib
|
Gsd-Vi
|
Liver Phosphorylase Deficiency
|
Storage Disease, Glycogen, Type Vi
|
|
|
Fanconi-Bickel Syndrome |
Glycogen Storage Disease Xi
|
Lactate Dehydrogenase A Deficiency
|
Hepatorenal Glycogenosis With Renal Fanconi Syndrome
|
Hepatic Glycogenosis With Amino Aciduria And Glucosuria
|
Fanconi Syndrome With Intestinal Malabsorption And Galactose Intolerance
|
Pseudo-Phlorizin Diabetes
|
Glycogen Storage Disease Due To Lactate Dehydrogenase M-Subunit Deficiency
|
FBS
|
Hepatic Glycogenosis With Fanconi Nephropathy
|
GSD11
|
Gsd Xi
|
Glycogen Storage Disease Due To Glut2 Deficiency
|
Glycogenosis Fanconi Type
|
Lactate Dehydrogenase Deficiency Type A
|
Glycogenosis, Fanconi Type
|
Fanconi Bickel Syndrome
|
Glut2 Deficiency
|
Gsd Due To Glut2 Deficiency
|
Glycogenosis Due To Glut2 Deficiency
|
Gsd Due To Lactate Dehydrogenase M-Subunit Deficiency
|
Glycogenosis Due To Lactate Dehydrogenase M-Subunit Deficiency
|
Ldh-M Subunit Deficiency
|
Glycogen Storage Disease 11
|
Storage Disease, Glycogen, Type Xi
|
Glycogenosis With Glucoaminophosphaturia
|
|
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Glycogen Storage Disease Iii |
Glycogen Storage Disease Type Iii
|
Forbes Disease
|
Cori Disease
|
Glycogen Storage Disease Iiia
|
Amylo-1,6-Glucosidase Deficiency
|
Glycogen Storage Disease Iiib
|
Limit Dextrinosis
|
GSD3
|
Agl Deficiency
|
Glycogen Debrancher Deficiency
|
Gde Deficiency
|
Glycogen Storage Disease Iiic
|
Debrancher Deficiency
|
Glycogen Storage Disease Type 3
|
Glycogenosis Type Iii
|
Glycogen Storage Disease Iiid
|
Amylo 1,6 Glucosidase Deficiency
|
Deficiency Of Debranching Enzyme
|
Deficiency Of Dextrin
|
Glycogen Storage Disease, Type Iii
|
Glycogen Debranching Enzyme Deficiency
|
Cori'S Disease
|
Gsd Iii
|
Glycogen Storage Disease Due To Glycogen Debranching Enzyme Deficiency
|
Cori-Forbes Disease
|
Gsd Due To Glycogen Debranching Enzyme Deficiency
|
Gsd Type 3
|
Gsdiii
|
Glycogenosis Due To Glycogen Debranching Enzyme Deficiency
|
Glycogenosis Type 3
|
Glycogen Storage Disease 3
|
Glycogen Debranching Enzyme Deficiency
|
Gsd-Iii
|
Gsd Iiia
|
Gsd Iiib
|
Gsd Iiic
|
Gsd Iiid
|
Storage Disease, Glycogen, Type Iii
|
|
|
Hyperglycemia |
|
|
Sudden Infant Death Syndrome |
SIDS
|
Sudden Infant Death Syndrome, Susceptibility To
|
Cot Death
|
Crib Death
|
Sudden Death Of Nonspecific Cause In Infancy
|
Sudden Infant Death
|
Death, Sudden, Syndrome, Infant
|
|
|
Severe Congenital Neutropenia 4 |
Autosomal Recessive Severe Congenital Neutropenia Due To G6pc3 Deficiency
|
Scn4
|
Severe Congenital Neutropenia-Pulmonary Hypertension-Superficial Venous Angiectasis Syndrome
|
Dursun Syndrome
|
Severe Congenital Neutropenia Type 4
|
|
|
Liver Benign Neoplasm |
Epithelial Hepatic And Intrahepatic Bile Duct Neoplasm
|
|
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Neutropenia |
|
|
Glycogen Storage Disease Iv |
Gsd Iv
|
Glycogen Branching Enzyme Deficiency
|
Andersen Disease
|
Amylopectinosis
|
Glycogen Storage Disease Type Iv
|
GSD4
|
Brancher Deficiency
|
Glycogen Storage Disease, Type Iv
|
Glycogen Storage Disease Due To Glycogen Branching Enzyme Deficiency, Congenital Neuromuscular Form
|
Gbe1 Deficiency
|
Glycogenosis Iv
|
Cirrhosis, Familial, With Deposition Of Abnormal Glycogen
|
Glycogen Storage Disease Type 4
|
Glycogenosis 4
|
Potassium-Sensitive Periodic Paralysis, Ventricular Ectopy, And Dysmorphic Features
|
Andersen'S Disease
|
Glycogen Storage Disease Due To Glycogen Branching Enzyme Deficiency, Childhood Neuromuscular Form
|
Glycogen Storage Disease Due To Glycogen Branching Enzyme Deficiency, Fatal Perinatal Neuromuscular Form
|
Brancher Deficiency Glycogenosis
|
Branching-Transferase Deficiency Glycogenosis
|
Deficiency Of 1,4-Alpha-Glucan Branching Enzyme
|
Andersen-Tawil Syndrome
|
Gsd 4
|
Andersen Cardiodysrhythmic Periodic Paralysis
|
Lqt7
|
Long Qt Syndrome 7
|
Periodic Paralysis, Potassium-Sensitive Cardiodysrhythmic Type
|
Andersen Glycogenosis
|
Branching Enzyme Deficiency
|
Glycogenosis, Type Iv
|
Gsd Type Iv
|
Type Iv Glycogenosis
|
Gbe Deficiency, Childhood Neuromuscular Form
|
Gsd Due To Glycogen Branching Enzyme Deficiency, Childhood Neuromuscular Form
|
Gsd Type 4, Childhood Neuromuscular Form
|
Gsdiv, Childhood Neuromuscular Form
|
Glycogen Storage Disease Type 4, Childhood Neuromuscular Form
|
Glycogen Storage Disease Type Iv, Childhood Neuromuscular Form
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Glycogenosis Due To Glycogen Branching Enzyme Deficiency, Childhood Neuromuscular Form
|
Glycogenosis Type 4, Childhood Neuromuscular Form
|
Glycogenosis Type Iv, Childhood Neuromuscular Form
|
Glycogen Storage Disease Due To Glycogen Branching Enzyme Deficiency, Adult Neuromuscular Form
|
Gbe Deficiency, Adult Neuromuscular Form
|
Gsd Due To Glycogen Branching Enzyme Deficiency, Adult Neuromuscular Form
|
Gsd Type 4, Adult Neuromuscular Form
|
Gsdiv, Adult Neuromuscular Form
|
Glycogen Storage Disease Type 4, Adult Neuromuscular Form
|
Glycogen Storage Disease Type Iv, Adult Neuromuscular Form
|
Glycogenosis Due To Glycogen Branching Enzyme Deficiency, Adult Neuromuscular Form
|
Glycogenosis Type 4, Adult Neuromuscular Form
|
Glycogenosis Type Iv, Adult Neuromuscular Form
|
Gbe Deficiency, Congenital Neuromuscular Form
|
Gsd Due To Glycogen Branching Enzyme Deficiency, Congenital Neuromuscular Form
|
Gsd Type 4, Congenital Neuromuscular Form
|
Gsdiv, Congenital Neuromuscular Form
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Glycogen Storage Disease Type 4, Congenital Neuromuscular Form
|
Glycogen Storage Disease Type Iv, Congenital Neuromuscular Form
|
Glycogenosis Due To Glycogen Branching Enzyme Deficiency, Congenital Neuromuscular Form
|
Glycogenosis Type 4, Congenital Neuromuscular Form
|
Glycogenosis Type Iv, Congenital Neuromuscular Form
|
Glycogen Storage Disease Due To Glycogen Branching Enzyme Deficiency, Childhood Combined Hepatic And Myopathic Form
|
Gbe Deficiency, Childhood Combined Hepatic And Myopathic Form
|
Gsd Due To Glycogen Branching Enzyme Deficiency, Childhood Combined Hepatic And Myopathic Form
|
Gsd Type 4, Childhood Combined Hepatic And Myopathic Form
|
Gsdiv, Childhood Combined Hepatic And Myopathic Form
|
Glycogen Storage Disease Type 4, Childhood Combined Hepatic And Myopathic Form
|
Glycogen Storage Disease Type Iv, Childhood Combined Hepatic And Myopathic Form
|
Glycogenosis Due To Glycogen Branching Enzyme Deficiency, Childhood Combined Hepatic And Myopathic Form
|
Glycogenosis Type 4, Childhood Combined Hepatic And Myopathic Form
|
Glycogenosis Type Iv, Childhood Combined Hepatic And Myopathic Form
|
Gbe Deficiency, Fatal Perinatal Neuromuscular Form
|
Gsd Due To Glycogen Branching Enzyme Deficiency, Fatal Perinatal Neuromuscular Form
|
Gsd Type 4, Fatal Perinatal Neuromuscular Form
|
Gsdiv, Fatal Perinatal Neuromuscular Form
|
Glycogen Storage Disease Type 4, Fatal Perinatal Neuromuscular Form
|
Glycogen Storage Disease Type Iv, Fatal Perinatal Neuromuscular Form
|
Glycogenosis Due To Glycogen Branching Enzyme Deficiency, Fatal Perinatal Neuromuscular Form
|
Glycogenosis Type 4, Fatal Perinatal Neuromuscular Form
|
Glycogenosis Type Iv, Fatal Perinatal Neuromuscular Form
|
Glycogen Storage Disease Due To Glycogen Branching Enzyme Deficiency, Non Progressive Hepatic Form
|
Gbe Deficiency, Non Progressive Hepatic Form
|
Gsd Due To Glycogen Branching Enzyme Deficiency, Non Progressive Hepatic Form
|
Gsd Type 4, Non Progressive Hepatic Form
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Gsdiv, Non Progressive Hepatic Form
|
Glycogen Storage Disease Type 4, Non Progressive Hepatic Form
|
Glycogen Storage Disease Type Iv, Non Progressive Hepatic Form
|
Glycogenosis Due To Glycogen Branching Enzyme Deficiency, Non Progressive Hepatic Form
|
Glycogenosis Type 4, Non Progressive Hepatic Form
|
Glycogenosis Type Iv, Non Progressive Hepatic Form
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Glycogen Storage Disease Due To Glycogen Branching Enzyme Deficiency, Progressive Hepatic Form
|
Gbe Deficiency, Progressive Hepatic Form
|
Gsd Due To Glycogen Branching Enzyme Deficiency, Progressive Hepatic Form
|
Gsd Type 4, Progressive Hepatic Form
|
Gsdiv, Progressive Hepatic Form
|
Glycogen Storage Disease Type 4, Progressive Hepatic Form
|
Glycogen Storage Disease Type Iv, Progressive Hepatic Form
|
Glycogenosis Due To Glycogen Branching Enzyme Deficiency, Progressive Hepatic Form
|
Glycogenosis Type 4, Progressive Hepatic Form
|
Glycogenosis Type Iv, Progressive Hepatic Form
|
Glycogen Storage Disease 4
|
Gsd-Iv
|
Storage Disease, Glycogen, Type Iv
|
|
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Type 2 Diabetes Mellitus |
Insulin Resistance
|
NIDDM
|
Type 2 Diabetes
|
Diabetes Mellitus, Non-Insulin-Dependent
|
T2D
|
Noninsulin-Dependent Diabetes Mellitus
|
Diabetes Mellitus, Type Ii
|
Maturity-Onset Diabetes
|
Insulin Resistance, Severe, Digenic
|
Diabetes Mellitus, Type 2
|
Diabetes Mellitus, Noninsulin-Dependent
|
Diabetes Mellitus, Noninsulin-Dependent, Association With
|
Diabetes Mellitus, Noninsulin-Dependent, Late Onset
|
Hypertension, Insulin Resistance-Related, Susceptibility To
|
Insulin Resistance, Susceptibility To
|
Non-Insulin-Dependent Diabetes Mellitus
|
Type Ii Diabetes Mellitus
|
Adult-Onset Diabetes Mellitus
|
Maturity-Onset Diabetes Mellitus
|
Diabetes Mellitus Type 2
|
Type Ii Diabetes
|
Type 2 Diabetes Mellitus, Susceptibility To
|
Diabetes, Type 2
|
Diabetes Mellitus, Noninsulin-Dependent, Susceptibility To
|
Diabetes Mellitus, Non-Insulin-Dependent, Susceptibility To
|
Diabetes Mellitus, Type 2, Susceptibility To
|
Diabetes Mellitus, Noninsulin-Dependent, 2
|
Diabetes Mellitus, Type Ii, Susceptibility To
|
Hypertension, Insulin Resistance-Related
|
Adult-Onset Diabetes
|
Aodm
|
Diabetes Mellitus, Adult-Onset
|
Diabetes Mellitus Type Ii
|
Diabetes Mellitus Type 2, Susceptibility To
|
Diabetes, Type Ii, Susceptibility To
|
Diabetes Type 2
|
Diabetes Mellitus
|
Adult Onset Diabetes
|
Maturity Onset Diabetes
|
Nonketotic Diabetes
|
Non-Insulin Dependent Diabetes Mellitus
|
T2dm - [Type 2 Diabetes Mellitus]
|
Niddm - [Non Insulin Dependent Diabetes Mellitus]
|
Dm2
|
Dm Type Ii
|
Diabetic Type 2
|
Insulin Requiring Type 2 Diabetes
|
Noninsulin Dependent Diabetes
|
Non-Insulin-Dependent Diabetes Mellitus Without Complications
|
Diabetes Due To Insulin Secretory Defect
|
Diabetes Mellitus Due To Insulin Secretory Defect
|
Non-Insulin-Dependent Diabetes Of The Young
|
Senile Diabetes
|
Nonketotic Hyperglycaemia
|
Stable Diabetes
|
|
|
Fructose-1,6-Bisphosphatase Deficiency |
Fructose-1,6-Diphosphatase Deficiency
|
Baker-Winegrad Disease
|
FBP1D
|
Fbpase Deficiency
|
Fructose 1,6 Diphosphatase Deficiency
|
Fructose 1 Phosphate Aldolase Deficiency
|
Fbp1 Deficiency
|
Hereditary Fructose Intolerance Syndrome
|
|
|
Insulinoma |
Islet Cell Adenoma
|
Insulin-Producing Tumor Of Islet Cells
|
Adenoma Islet Cell
|
Islet Cell Tumor
|
Experimental Organism Islet Cell Adenoma Neoplasm
|
|
|
Extragonadal Nonseminomatous Germ Cell Tumor |
Primary Malignant Extragonadal Nonseminoma
|
Malignant Extragonadal Non-Seminomatous Germ Cell Tumor
|
|
|
Diabetes Mellitus |
|
|
Abdominal Obesity-Metabolic Syndrome 1 |
Metabolic Syndrome X
|
Metabolic Syndrome
|
AOMS1
|
Dysmetabolic Syndrome X
|
Metabolic Disease
|
Abdominal Obesity Metabolic Syndrome
|
|
|
Hemochromatosis, Type 1 |
Hemochromatosis
|
Hemochromatosis Type 1
|
Hereditary Hemochromatosis
|
Hh
|
HFE1
|
Hfe Hemochromatosis, Modifier Of
|
Symptomatic Form Of Classic Hemochromatosis
|
Symptomatic Form Of Hemochromatosis Type 1
|
Symptomatic Form Of Hfe-Related Hereditary Hemochromatosis
|
Haemochromatosis
|
Iron Storage Disorder
|
Bronze Diabetes
|
Hereditary Haemochromatosis
|
Hlah
|
Hfe
|
Hemochromatosis, Hereditary
|
Diabetes Bronze
|
Classic Hemochromatosis
|
Hfe-Associated Hereditary Hemochromatosis
|
Hemochromatosis Classic
|
Bronzed Cirrhosis
|
Familial Hemochromatosis
|
Genetic Hemochromatosis
|
Hc
|
Pigmentary Cirrhosis
|
Primary Hemochromatosis
|
Troisier-Hanot-Chauffard Syndrome
|
Von Recklenhausen-Applebaum Disease
|
Hemochromatosis 1
|
Primary Hereditary Hemochromatosis
|
Bronze Cirrhosis
|
|
|
Hepatocellular Carcinoma |
Liver Cancer
|
Primary Liver Cancer
|
HCC
|
Hepatoma
|
Malignant Neoplasm Of Liver
|
Liver Neoplasms
|
Cancer, Hepatocellular
|
Liver Cell Carcinoma
|
Lcc
|
Hepatoblastoma, Somatic
|
Hepatic Cancer
|
Primary Malignant Neoplasm Of Liver
|
Rare Tumor Of Liver And Intrahepatic Biliary Tract
|
Hepatocellular Carcinoma, Somatic
|
Hepatocellular Carcinoma, Childhood Type, Somatic
|
Hepatocellular Cancer, Somatic
|
Ca Liver - Primary
|
Hepatic Neoplasm
|
Malignant Hepato-Biliary Neoplasm
|
Malignant Neoplasm Of Liver, Not Specified As Primary Or Secondary
|
Malignant Neoplasm Of Liver, Primary
|
Malignant Tumor Of Liver
|
Neoplasm Of Liver
|
Non-Resectable Primary Hepatic Malignant Neoplasm
|
Resectable Malignant Neoplasm Of Liver
|
Resectable Malignant Neoplasm Of The Liver
|
Primary Liver Carcinoma
|
Primary Malignant Liver Neoplasm
|
Primary Cancer Of Liver
|
Primary Tumor Of The Liver
|
Rare Tumor Of Liver And Ibt
|
Hepatocellular Cancer
|
Neoplasm Of The Liver
|
Carcinoma, Hepatocellular
|
Hepatomas
|
Liver Neoplasm
|
Liver Carcinoma
|
Liver And Intrahepatic Biliary Tract Carcinoma
|
Malignant Hepatobiliary Neoplasm
|
Adult Primary Hepatocellular Carcinoma
|
Hepatoblastoma
|
Carcinoma Of Liver
|
Malignant Liver Tumour
|
Malignant Hepatic Tumour
|
|
|
Intellectual Developmental Disorder, X-Linked 108 |
MRX108
|
X-Linked Intellectual Developmental Disorder 108
|
Mental Retardation, X-Linked 108
|
Mental Retardation, X-Linked, Type 108
|
|
|
Severe Congenital Neutropenia |
Congenital Neutropenia
|
Neutropenia, Severe Congenital
|
Congenital Agranulocytosis
|
Infantile Genetic Agranulocytosis
|
Kostmann Disease
|
Kostmann'S Agranulocytosis
|
Kostmann'S Syndrome
|
Severe Infantile Genetic Neutropenia
|
|
|
Lactic Acidosis |
Acidosis, Lactic
|
Acidosis Lactic
|
|
|
Lipid Metabolism Disorder |
Dyslipidemia
|
Disorder Of Fatty Acid Metabolism
|
Lipid Metabolism Disorders
|
Fatty Acid Metabolism Disorder
|
Disorder Of Lipid Metabolism
|
Abnormality Of Lipid Metabolism
|
Lipid Metabolism, Inborn Errors
|
Dyslipidemias
|
Disorders Of Lipid Metabolism
|
Congenital Disorders Of Lipid Metabolism
|
Inherited Disorders Of Lipid Metabolism
|
|
|
Maturity-Onset Diabetes Of The Young |
MODY
|
Maturity Onset Diabetes Mellitus In Young
|
Mason-Type Diabetes
|
Mason Type Diabetes
|
Maturity Onset Diabetes Of The Young
|
Mody Syndrome
|
Diabetes Of The Young, Maturity-Onset
|
|
|
Body Mass Index Quantitative Trait Locus 11 |
OBESITY
|
Obesity, Susceptibility To
|
Leanness, Inherited
|
Obesity, Susceptibility To, Bmiq11
|
Obesity, Mild, Early-Onset
|
Obesity, Association With
|
Obesity, Early-Onset, Susceptibility To
|
Obesity, Severe
|
Obesity, Severe, And Type Ii Diabetes
|
Obesity, Late-Onset
|
Obesity , Susceptibility To
|
BMIQ11
|
Obesity Bmiq11
|
Obesity, Early-Onset
|
Simple Obesity Nos
|
Excess Fat
|
Obesity, Not Elsewhere Classified, Body Mass Index Not Elsewhere Classified
|
Adiposis
|
|
|