Diseases |
Alias |
|
Psoriasis |
|
|
Cardiovascular System Disease |
Abnormality Of The Cardiovascular System
|
Disease Of Subdivision Of Hemolymphoid System
|
Disorder Of Cardiovascular System
|
Cardiovascular Diseases
|
Cardiovascular Disease
|
|
|
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
|
BMIQ11
|
Obesity Bmiq11
|
Obesity, Early-Onset
|
Obesity , Susceptibility To
|
Simple Obesity Nos
|
Excess Fat
|
Obesity, Not Elsewhere Classified, Body Mass Index Not Elsewhere Classified
|
Adiposis
|
|
|
Amelogenesis Imperfecta |
Ai
|
Congenital Enamel Hypoplasia
|
Al - [Amelogenesis Imperfecta]
|
|
|
Lipoprotein Quantitative Trait Locus |
Coronary Artery Disease
|
Coronary Artery Disease, Susceptibility To
|
Coronary Artery Anomaly
|
Myocardial Ischemia
|
Congenital Anomaly Of Coronary Artery
|
Coronary Arteriosclerosis
|
Coronary Disease
|
Coronary Heart Disease
|
Coronary Artery Disorder
|
LPAQTL
|
Lpa Deficiency, Congenital
|
Coronary Artery Abnormality
|
Coronary Artery Anomaly, Congenital
|
Chd
|
Coronary Syndrome
|
Congenital Malformations Of Coronary Vessels
|
Malformation Of Coronary Vessels
|
Congenital Coronary Artery Anomaly
|
Congenital Coronary Artery Deformity
|
Congenital Coronary Artery Disorder
|
Abnormal Coronary Artery
|
Congenital Coronary Artery Malposition
|
Congenital Coronary Disease
|
Congenital Anomaly Of Coronary Arteries
|
|
|
Hypoalphalipoproteinemia |
|
|
Lysosomal Storage Disease |
Lysosomal Storage Diseases
|
Disorder Of Lysosomal Enzyme
|
Inborn Lysosomal Enzyme Disorder
|
Lysosomal Storage Metabolism Disorder
|
Lysosomal Storage Disorder
|
|
|
Hyperlipidemia, Familial Combined, 3 |
Familial Combined Hyperlipidemia
|
Combined Hyperlipidemia, Familial
|
Mixed Hyperlipidaemia
|
FCHL3
|
Hyperlipidemia, Familial Combined
|
Familial Multiple Lipoprotein-Type Hyperlipidemia
|
Hyperbetalipoproteinemia With Prebetalipoproteinemia
|
Type Iib Hyperlipoproteinemia
|
Hyperlipidemia Familial Combined
|
Hyperlipoproteinemia Type Iib
|
Mixed Hyperlipemia
|
Hyperlipidaemia, Group C
|
Familial Hypercholesterolaemia With Hyperlipaemia
|
Familial Hyperbetalipoproteinaemia And Hyperprebetalipoproteinaemia
|
Hyperbetalipoproteinaemia With Prebetalipoproteinaemia
|
Hypercholesterolaemia With Endogenous Hyperglyceridaemia
|
Prebetalipoproteinemia Hyperbetalipoproteinaemia
|
Remnant Hyperlipoproteinemia
|
|
|
Bilirubin Metabolic Disorder |
Hyperbilirubinemia
|
Hereditary Hyperbilirubinemia
|
Hyperbilirubinemia, Hereditary
|
Hyperbilirubinaemia
|
|
|
Myopathy |
Muscular Diseases
|
Myopathies
|
|
|
Overnutrition |
|
|
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
|
|
|
Multiple Sclerosis |
MS
|
Multiple Sclerosis, Susceptibility To
|
Disseminated Sclerosis
|
Multiple Sclerosis, Disease Progression, Modifier Of
|
Insular Sclerosis
|
Multiple Sclerosis Modifier Of Disease Progression
|
Multiple Sclerosis, Susceptibility To 1
|
Multiple Sclerosis, Susceptibility To, 1
|
Multiple Sclerosis 1
|
Generalized Multiple Sclerosis
|
Multiple Sclerosis Variant
|
Multiple Sclerosis Susceptibility To
|
Cerebrospinal Sclerosis
|
Generalised Multiple Sclerosis
|
Ms - [Multiple Sclerosis]
|
Disseminated Cerebrospinal Sclerosis
|
Disseminated Multiple Sclerosis
|
Disseminated Nervous System Myelosclerosis
|
Multiple Cerebrospinal Sclerosis
|
Multiple Combined Sclerosis
|
Multiple Sclerosis Generalised
|
Disseminated Brain Sclerosis
|
Disseminated Spinal Sclerosis
|
Insular Brain Sclerosis
|
Miliary Brain Sclerosis
|
Multiple Combined Sclerosis Of Spinal Cord
|
Multiple Ascending Sclerosis
|
Multiple Brain Sclerosis
|
Multiple Sclerosis Of Brain Stem
|
Multiple Sclerosis Of The Brain Stem
|
Multiple Sclerosis Of Cord
|
Sclérose En Plaques
|
Plaque Sclerosis
|
Multiple Sclerosis Of The Spinal Cord
|
|
|
Adult Syndrome |
Acro-Dermato-Ungual-Lacrimal-Tooth Syndrome
|
Acro Dermato Ungual Lacrimal Tooth Syndrome
|
Pigment Anomaly-Ectrodactyly-Hypodontia Syndrome
|
Acro-Dermato-Ungual-Lacrimal-Tooth Syndrome
|
Adult
|
|
|
Hypertensive Heart Disease |
|
|
Glucose Metabolism Disease |
Glucose Metabolism Disorders
|
Disorder Of Glucose Metabolism
|
|
|
Hypertension, Essential |
Essential Hypertension
|
Hypertension
|
High Blood Pressure
|
Hypertension, Essential, Susceptibility To
|
Hypertensive Disease
|
Primary Hypertension
|
EHT
|
Hypertension, Salt-Sensitive Essential, Susceptibility To
|
Hyperpiesia
|
Idiopathic Hypertension
|
Hypertensive Disorder
|
Hypertension, Essential, Susceptibility To, 3
|
Hypertension, Essential 3
|
Hypertension, Essential, Salt-Sensitive
|
Hypertension, Essential, Susceptibility To, 6
|
Hypertension, Essential 6
|
Hypertension, Salt-Sensitive Essential
|
Hypertension, Susceptibility To
|
Hypertension, Essential, Susceptibility To, 4
|
Hypertension, Essential 4
|
Hypertension, Essential, Susceptibility To, 2
|
Hypertension, Essential 2
|
Hypertension, Essential, Susceptibility To, 1
|
Hypertension, Essential 1
|
Hypertension, Essential, Susceptibility To, 5
|
Hypertension, Essential 5
|
Htn
|
Vascular Hypertensive Disorder
|
Systemic Primary Arterial Hypertension
|
Hbp - [High Blood Pressure]
|
Systemic Arterial Hypertensive Disorder
|
Elevated Blood Pressure
|
Arterial Hypertension Nos
|
Hypertension Nos
|
Benign Hypertension
|
Systemic Arterial Hypertension
|
Systemic Hypertension
|
Artery Htn
|
Benign Htn
|
Vascular Htn
|
Vascular Hypertension
|
Cholesterol Hypertension
|
Cholesterol Htn
|
Idiopathic Htn
|
Malignant Hypertension
|
Malignant Htn
|
Raised Blood Pressure
|
Cardiovascular Hypertension
|
Primary Htn - [Hypertension]
|
High Arterial Tension
|
High Blood Pressure Disorder
|
Ht - [Hypertension]
|
Htn - [Hypertension]
|
Hypertensive Vascular Disease
|
Hypertensive Vascular Degeneration
|
|
|
Fatty Liver Disease |
Alcoholic Fatty Liver
|
Fatty Liver
|
Fatty Liver, Alcoholic
|
Fatty Change Of Liver
|
Hepatic Lipidosis
|
Steatosis Of Liver
|
Fatty Liver Alcoholic
|
Steatohepatitis
|
Etoh Fatty Liver
|
Etoh Fatty Liver Metamorphosis
|
Fatty Etoh Liver Necrosis
|
|
|
Diabetes Mellitus |
|
|
Respiratory Failure |
Acute Respiratory Failure
|
Chronic Respiratory Failure
|
Respiratory Insufficiency
|
Acute-On-Chronic Respiratory Failure
|
Acute And Chronic Respiratory Failure
|
Respiratory Insufficiency/Failure
|
Chronic Respiratory Disease
|
Respiratory Disease
|
Pulmonary Valve Insufficiency
|
Chronic Disease Of Respiratory System
|
Respiration Disorders
|
Respiratory Tract Diseases
|
Lung Failure Nos
|
Pulmonary Failure
|
Arf - [Acute Respiratory Failure]
|
Acute Respiratory Insufficiency
|
Acute Pulmonary Insufficiency
|
Acute Respiration Failure
|
Chronic Respiration Failure
|
|
|
Dilated Cardiomyopathy |
Familial Dilated Cardiomyopathy
|
Primary Dilated Cardiomyopathy
|
Idiopathic Dilated Cardiomyopathy
|
Congestive Cardiomyopathy
|
Idiopathic Dilation Cardiomyopathy
|
Primary Familial Dilated Cardiomyopathy
|
Cardiomyopathy, Dilated
|
DCM
|
Cardiomyopathy, Familial Dilated
|
Dilated Cardiomyopathy, Familial
|
Hypokinetic Dilated Cardiomyopathy, Familial
|
Familial Idiopathic Cardiomyopathy
|
Fdc
|
Cardiomyopathy, Familial Idiopathic
|
Idiopathic Cardiomegaly
|
Dilated Congestive Cardiomyopathy
|
Chronic Dilated Cardiomyopathy
|
Ccm - [Congestive Cardiomyopathy]
|
Cocm - [Congestive Cardiomyopathy]
|
Dcm - [Dilated Cardiomyopathy]
|
Dilated-Hypokinetic Cardiomyopathy
|
Congestive Idiopathic Cardiomyopathy
|
Primary Idiopathic Dilated Cardiomyopathy
|
|
|
Peroxisomal Biogenesis Disorder |
Zellweger Spectrum Disorders
|
Peroxisome Biogenesis Disorder-Zellweger Syndrome Spectrum
|
Disorders Of Peroxisome Biogenesis
|
Zellweger Spectrum
|
Zellweger Syndrome Spectrum
|
Peroxisomal Biogenesis Disorders
|
Pbd, Zss
|
Pbd-Zsd
|
Pbd-Zss
|
Pbd-Zellweger Spectrum Disorder
|
Peroxisomal Biogenesis Disorders, Zellweger Syndrome Spectrum
|
Peroxisome Biogenesis Disorder
|
Peroxisome Biogenesis Disorder Spectrum
|
Peroxisome Biogenesis Disorders
|
Zellweger Spectrum Disorder
|
Hyperpipecolic Acidaemia
|
|
|
Lipid Storage Disease |
Lipoidosis
|
Inborn Lipid Storage Disorder
|
Lipoid Storage Diseas
|
Lipid Storage Diseases
|
Lipidoses
|
|
|
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
|
|
|
Deficiency Anemia |
Anemia
|
Deficiency Anemias
|
Anaemia
|
|
|
Abdominal Obesity-Metabolic Syndrome 1 |
Metabolic Syndrome X
|
Metabolic Syndrome
|
AOMS1
|
Dysmetabolic Syndrome X
|
Metabolic Disease
|
Abdominal Obesity Metabolic Syndrome
|
|
|
Non-Alcoholic Fatty Liver Disease |
Fatty Liver
|
Non-Alcoholic Fatty Liver
|
Nafld
|
Nonalcoholic Fatty Liver Disease
|
Nonalcoholic Steatohepatitis
|
Steatosis
|
Nafl
|
Nash
|
Non-Alcoholic Steatohepatitis
|
Susceptibility To Nonalcoholic Fatty Liver Disease
|
Steatohepatitis
|
Fatty Degeneration
|
Non-Alcoholic Fatty Liver Disease Without Mention Of Non-Alcoholic Steatohepatitis
|
Nafld Without Nash
|
Nafld Without Mention Of Nash
|
|
|
Dermatitis |
Eczema
|
Skin Inflammation
|
Inflammatory Dermatosis
|
|
|
Liposarcoma |
|
|
Headache |
|
|
Atherosclerosis Susceptibility |
Atherosclerosis
|
Atherosclerosis, Susceptibility To
|
ATHS
|
Atherogenic Lipoprotein Phenotype
|
Alp
|
Arteriosclerosis
|
|
|
Adrenoleukodystrophy |
X-Linked Adrenoleukodystrophy
|
ALD
|
Siemerling-Creutzfeldt Disease
|
X-Ald
|
X-Linked Cerebral Adrenoleukodystrophy
|
Bronze Schilder Disease
|
Melanodermic Leukodystrophy
|
Addison Disease And Cerebral Sclerosis
|
Adrenomyeloneuropathy, Adult
|
Diffuse Sclerosis
|
X-Cald
|
Adrenomyeloneuropathy
|
Encephalitis Periaxialis Concentrica
|
Encephalitis Periaxialis, Schilder'S
|
Sudanophilic Cerebral Sclerosis
|
Ald Childhood Cerebral Form
|
Adrenoleukodystrophy X-Linked Cerebral Form
|
Adrenoleukodystrophy Childhood Cerebral Form
|
Childhood Cerebral Ald
|
Schilder Disease
|
X-Linked Ald
|
Adrenoleukodystrophy, X-Linked
|
Amn
|
Diffuse Cerebral Sclerosis Of Schilder
|
Systemic Scleroderma
|
Balo'S Concentric Sclerosis
|
Ald - [Adrenoleukodystrophy]
|
Addison-Schilder
|
|
|
Familial Hyperlipidemia |
Familial Hyperlipoproteinemia
|
Hyperlipidaemia
|
Hyperlipoproteinemias
|
Hyperlipemia
|
Hyperlipidemias
|
Hyperlipidemia
|
|
|
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
|
|
|
Chanarin-Dorfman Syndrome |
Neutral Lipid Storage Disease
|
CDS
|
Neutral Lipid Storage Disease With Ichthyosis
|
Triglyceride Storage Disease With Impaired Long-Chain Fatty Acid Oxidation
|
Triglyceride Storage Disease With Ichthyosis
|
Nlsdi
|
Ichthyotic Neutral Lipid Storage Disease
|
Dcs
|
Chanarin-Dorfman Disease
|
Ichthyosiform Erythroderma With Leukocyte Vacuolation
|
Dorfman-Chanarin Syndrome
|
Lipidosis With Triglyceride Storage Disease
|
Disorder Of Cornification 12
|
Dorfman Chanarin Syndrome
|
Neutral Lipid Storage Disease With Ichthyotic
|
Dorfman-Chanarin Disease
|
|
|
Acute Tympanitis |
|
|
Tularemia |
Francisella Tularensis Infection
|
Deerfly Fever
|
Lemming Fever
|
Ohara Disease
|
Pahvant Valley Plague
|
Rabbit Fever
|
Yatobyo
|
|
|
Vascular Disease |
Vascular Diseases
|
Aneurysm
|
Spinal Cord Ischemia
|
Spinal Cord Vascular Diseases
|
Vascular Tissue Disease
|
Vascular Anomaly
|
|
|
Liver Benign Neoplasm |
Epithelial Hepatic And Intrahepatic Bile Duct Neoplasm
|
|
|
Parkinson Disease, Late-Onset |
Parkinson Disease
|
Parkinson'S Disease
|
PD
|
PARK
|
Parkinson Disease, Susceptibility To
|
Late Onset Parkinson'S Disease
|
Late Onset Parkinson Disease
|
Paralysis Agitans
|
Primary Parkinsonism
|
Idiopathic Parkinson Disease
|
Parkinson'S
|
Parkinson Disease, Late-Onset, Susceptibility To
|
Parkinson Disease, Age Of Onset, Modifier
|
Lewy Body Parkinson Disease
|
Idiopathic Parkinson'S Disease
|
Pd - [Parkinson Disease]
|
Parkinson Disease Nos
|
Parkinson, Nos
|
Primary Parkinson Disease
|
|
|
Inflammatory Bowel Disease |
Inflammatory Bowel Diseases
|
Bowel Disease, Inflammatory
|
|
|
Schizophrenia 16 |
SCZD16
|
Schizophrenia Susceptibility Locus, Chromosome 7q36.3-Related
|
Chromosome 7q36.3 Duplication Syndrome, 362-Kb
|
|
|
Non-Alcoholic Steatohepatitis |
Nonalcoholic Steatohepatitis
|
Nash
|
Nash - [Non-Alcoholic Steatohepatitis]
|
Non-Alcoholic Steatohepatosis
|
|
|
Alzheimer Disease 11 |
Ad11
|
Alzheimer'S Disease 11
|
Alzheimer Disease, Familial, 11
|
Alzheimer Disease-11
|
Alzheimer'S Disease 11, Late Onset
|
|
|
Carbohydrate Metabolic Disorder |
Inborn Errors Of Carbohydrate Metabolism
|
Disorder Of Carbohydrate Metabolism
|
Carbohydrate Metabolism, Inborn Errors
|
Disorder Of Carbohydrate Transport And Metabolism
|
Inborn Carbohydrate Metabolism Disorder
|
Inborn Carbohydrate Metabolic Disorder
|
Carbohydrate Metabolism Disorder
|
Carbohydrate Metabolism Disorders
|
Disorders Of Carbohydrate Metabolism
|
Congenital Disorders Of Carbohydrate Metabolism
|
Inherited Disorders Of Carbohydrate Metabolism
|
|
|
Leptin Deficiency Or Dysfunction |
Morbid Obesity
|
Obesity Due To Congenital Leptin Deficiency
|
LEPD
|
Congenital Leptin Deficiency
|
Obesity, Morbid
|
Obesity, Morbid, Due To Leptin Deficiency
|
Severe Obesity
|
Obesity, Morbid, Nonsyndromic 1
|
Leptin Deficiency
|
Obesity, Severe, Due To Leptin Deficiency
|
Morbid Obesity Due To Leptin Deficiency
|
Obesity Morbid
|
Leptin Dysfunction
|
Leptin
|
|
|
Nervous System Disease |
Abnormality Of The Nervous System
|
Nervous System Diseases
|
Nervous System Disorder
|
|
|
Abdominal Obesity-Metabolic Syndrome Quantitative Trait Locus 2 |
Abdominal Obesity-Metabolic Syndrome
|
Abdominal Obesity Metabolic Syndrome
|
Metabolic Syndrome X
|
Aoms2
|
Aoms1
|
|
|
Heart Disease |
Heart Failure
|
Congenital Heart Disease
|
Heart Diseases
|
Congenital Heart Defects
|
Congenital Heart Defect
|
Congenital Anomaly Of Heart
|
Heart Defect
|
Heart Malformation
|
Heart-Congenital Defect
|
Congenital Heart Disorder
|
Heart Defects Congenital
|
Heart Defects, Congenital
|
Heart Defects
|
Heart Disease, Congenital
|
Disease, Heart, Congenital
|
Congestive Heart Failure
|
|
|
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
|
|
|
Gilbert Syndrome |
Gilbert Disease
|
Gilbert'S Disease
|
Gilbert'S Syndrome
|
Cholemia, Familial
|
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
|
Familial Nonhemolytic Jaundice
|
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
|
|
|
Alzheimer Disease, Familial, 1 |
Alzheimer Disease
|
Alzheimer'S Disease
|
Presenile And Senile Dementia
|
AD1
|
Alzheimer Disease, Susceptibility To
|
Alzheimer Disease, Late-Onset, Susceptibility To
|
Alzheimer Disease 1, Familial
|
AD
|
Familial Alzheimer Disease
|
Alzheimer Disease, Late-Onset
|
Alzheimers Dementia
|
Alzheimer Dementia
|
Alzheimer Sclerosis
|
Alzheimer Syndrome
|
Alzheimer-Type Dementia
|
Dat
|
Primary Senile Degenerative Dementia
|
Sdat
|
Alzheimer Disease 1
|
Autosomal Dominant Alzheimer Disease
|
Early-Onset Alzheimer Disease With Cerebral Amyloid Angiopathy
|
Late Onset Alzheimer Disease
|
Alzheimers Disease
|
Alzheimer Disease, Early-Onset, With Cerebral Amyloid Angiopathy
|
Late-Onset Alzheimers Disease
|
Alzheimer'S Disease Pathway Kegg
|
Dementia Due To Alzheimer'S Disease
|
Alzheimer Disease Type 1
|
Alzheimers
|
|
|
Hypertrophic Cardiomyopathy |
Hypertrophic Obstructive Cardiomyopathy
|
Cardiomyopathy, Hypertrophic
|
Cardiomyopathy, Hypertrophic, Familial
|
Familial Hypertrophic Cardiomyopathy
|
Cardiomyopathy Hypertrophic Obstructive
|
Idiopathic Myocardial Hypertrophy
|
Idiopathic Hypertrophic Cardiomyopathy
|
Obstructive Idiopathic Hypertrophic Cardiomyopathy
|
Obstructive Cardiomyopathy
|
Idiopathic Hypertrophic Subaortic Stenosis
|
Muscular Subaortic Stenosis
|
Hypertrophic Obstructive Subaortic Stenosis
|
|
|
Familial Partial Lipodystrophy |
Lipodystrophy, Familial Partial
|
Fpld
|
Kobberling-Dunnigan Syndrome
|
Dunnigan Syndrome
|
Koberling-Dunnigan Syndrome
|
Dunnigan-Kobberling Syndrome
|
Fpl
|
Familial Partial Lipodystrophy, Type 2
|
|
|
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
|
|
|
Platelet Glycoprotein Iv Deficiency |
Platelet-Type Bleeding Disorder 10
|
Bdplt10
|
Cd36 Deficiency
|
Bleeding Disorder, Platelet-Type, 10
|
PG4D
|
Bleeding Disorder Platelet-Type 10
|
Deficiency, Platelet Glycoprotein Iv
|
|
|
Inherited Metabolic Disorder |
Inborn Errors Of Metabolism
|
Inborn Metabolism Disorder
|
Metabolic Hereditary Disorder
|
Inborn Error Of Metabolism
|
Inborn Metabolic Disorder
|
Metabolism, Inborn Errors
|
|
|
Type 2 Diabetes Mellitus |
Insulin Resistance
|
NIDDM
|
Diabetes Mellitus, Non-Insulin-Dependent
|
Type 2 Diabetes
|
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
|
|
|
Myocardial Infarction |
Heart Attack
|
Myocardial Infarction, Susceptibility To
|
Myocardial Infarction 1
|
Myocardial Infarction, Protection Against
|
Myocardial Infarction, Decreased Susceptibility To
|
Myocardial Infarction, Decreased
|
Myocardial Infarct
|
MCI1
|
Premature Myocardial Infarction
|
Myocardial Infarction, Susceptibility To, Type 1
|
|
|
Hepatocellular Adenoma |
|
|
Proteasome-Associated Autoinflammatory Syndrome 1 |
Jmp Syndrome
|
Nakajo-Nishimura Syndrome
|
Nkjo
|
Autoinflammation, Lipodystrophy, And Dermatosis Syndrome
|
Proteasome-Associated Autoinflammatory Syndrome 1 And Digenic Forms
|
Nakajo Syndrome
|
PRAAS1
|
Chronic Atypical Neutrophilic Dermatosis With Lipodystrophy And Elevated Temperature Syndrome
|
Candle
|
Joint Contractures, Muscular Atrophy, Microcytic Anemia, And Panniculitis-Induced Lipodystrophy
|
Aldd
|
Joint Contractures - Muscle Atrophy - Microcytic Anemia - Panniculitis-Induced Lipodystrophy
|
Nakajo Nishimura Syndrome
|
Amyotrophy Fat Tissue Anomaly
|
Japanese Autoinflammatory Syndrome With Lipodystrophy
|
Jasl
|
Joint Contractures Muscular Atrophy Microcytic Anemia And Panniculitis-Induced Lipodystrophy
|
Nns
|
Nodular Erythema With Digital Changes
|
Secondary Hypertrophic Osteoperiostosis With Pernio
|
Inflammation
|
|
|
Cone-Rod Dystrophy 17 |
|
|
Schizophrenia |
SCZD
|
Schizophrenia With Or Without An Affective Disorder
|
Schizophrenia 12
|
Schizophrenia, Susceptibility To
|
Schizophrenia-1
|
Dementia Praecox
|
Schizophrenia 1
|
|
|
Zellweger Syndrome |
Cerebrohepatorenal Syndrome
|
Zellweger Leukodystrophy
|
Zs
|
Congenital Iron Overload
|
Peroxisome Biogenesis Disorder
|
Chr
|
Zws
|
Severe Pbd-Zsd
|
Severe Peroxisome Biogenesis Disorder-Zellweger Spectrum Disorder
|
|
|
Hepatoblastoma |
|
|
Hyperinsulinism |
|
|
Choline Deficiency Disease |
|
|
Arteriosclerosis |
Arteriosclerotic Vascular Disease
|
|
|
Acquired Metabolic Disease |
|
|
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
|
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
|
|
|
Arthritis |
Inflammatory Joint Disease
|
Inflammatory Disorder Of Joint
|
|
|
Alcoholic Hepatitis |
Acute Alcoholic Hepatitis
|
Acute Alcoholic Liver Disease
|
Hepatitis, Alcoholic
|
Hepatitis Alcoholic
|
Ah - [Alcoholic Hepatitis]
|
Ethanol Hepatitis
|
|
|
Skin Disease |
Skin Diseases
|
Abnormality Of The Skin
|
Skin Diseases, Genetic
|
Genodermatosis
|
Skin And Subcutaneous Tissue Disease
|
Dermatologic Disorders
|
|
|
Tangier Disease |
Analphalipoproteinemia
|
High Density Lipoprotein Deficiency, Tangier Type
|
TGD
|
High Density Lipoprotein Deficiency, Type 1
|
Hdldt1
|
Familial High Density Lipoprotein Deficiency
|
A-Alphalipoprotein Neuropathy
|
Alpha High Density Lipoprotein Deficiency Disease
|
Cholesterol Thesaurismosis
|
Familial High Density Lipoprotein Deficiency Disease
|
Hdl Lipoprotein Deficiency Disease
|
Tangier Disease Neuropathy
|
Familial Alpha-Lipoprotein Deficiency
|
Familial High-Density Lipoprotein Deficiency 1
|
Primary Hypoalphalipoproteinemia 1
|
Analphalipo-Proteinemia
|
Familial Hypoalphalipo-Proteinemia
|
Familial Hypoalphalipoproteinemia
|
Lipoprotein Deficiency Disease, Hdl, Familial
|
Tangier Hereditary Neuropathy
|
Atp-Binding Cassette Transporter A1 Deficiency
|
Hdld1
|
High Density Lipoprotein Deficiency 1
|
Tangier Disease, Variant
|
Hypoalphalipoproteinemia, Familial
|
Familial Hdl Deficiency
|
|
|