| 疾病名称 |
别名 |
|
| Coumarin Resistance |
|
Warfarin Resistance
|
Warfarin Sensitivity
|
|
Coumadin Sensitivity
|
Warfarin Response
|
|
Poor Metabolism Of Coumarin
|
Coumarin, Poor Metabolism Of
|
|
CMRES
|
|
|
| Epilepsy, Idiopathic Generalized 11 |
|
Epilepsy, Idiopathic Generalized, Susceptibility To, 11
|
EIG11
|
|
Epilepsy, Juvenile Absence 2
|
Epilepsy, Juvenile Myoclonic 8
|
|
Idiopathic Generalized Epilepsy 11
|
Epilepsy, Juvenile Absence, Susceptibility To, 2
|
|
Epilepsy, Juvenile Myoclonic, Susceptibility To, 8
|
Susceptibility To Idiopathic Generalized Epilepsy 11
|
|
Juvenile Absence Epilepsy 2
|
JAE2
|
|
Eja2
|
Susceptibility To Juvenile Absence Epilepsy 2
|
|
Juvenile Myoclonic Epilepsy 8
|
EJM8
|
|
Susceptibility To Juvenile Myoclonic Epilepsy 8
|
Epilepsy, Idiopathic, Generalized, Susceptibility To, Type 11
|
|
|
| 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
|
|
|
| Hemorrhagic Cystitis |
|
|
| Epilepsy, Idiopathic Generalized 10 |
|
EIG10
|
Epilepsy, Idiopathic Generalized, Susceptibility To, 10
|
|
Generalized Epilepsy With Febrile Seizures Plus, Type 5
|
Epilepsy, Juvenile Myoclonic, Susceptibility To
|
|
Epilepsy, Idiopathic Generalized, 10
|
Idiopathic Generalized Epilepsy 10
|
|
Epilepsy, Juvenile Myoclonic 7
|
Generalized Epilepsy With Febrile Seizures Plus Type 5
|
|
Generalized Epilepsy With Febrile Seizures Plus, Type 5, Susceptibility To
|
Epilepsy, Juvenile Myoclonic
|
|
Susceptibility To Idiopathic Generalized Epilepsy 10
|
Generalized Epilepsy With Febrile Seizures Plus 5
|
|
GEFS+5
|
Gefs+ Type 5
|
|
Gefsp5
|
Juvenile Myoclonic Epilepsy 7
|
|
EJM7
|
Susceptibility To Juvenile Myoclonic Epilepsy 7
|
|
Epilepsy, Idiopathic, Generalized, Susceptibility To, Type 10
|
Myoclonic Epilepsy, Juvenile
|
|
|
| Chronic Venous Insufficiency |
|
|
| Heart Disease |
|
Heart Failure
|
Congenital Heart Disease
|
|
Heart Diseases
|
Congenital Heart Defects
|
|
Congenital Heart Defect
|
Heart Malformation
|
|
Congenital Anomaly Of Heart
|
Heart Defect
|
|
Heart-Congenital Defect
|
Congenital Heart Disorder
|
|
Heart Defects Congenital
|
Heart Defects, Congenital
|
|
Heart Defects
|
Heart Disease, Congenital
|
|
Disease, Heart, Congenital
|
Congestive Heart Failure
|
|
|
| Neurotic Excoriation |
|
Factitious Skin Disease
|
Dermatitis Artefacta
|
|
Dermatitis Factitia
|
Dermatitis Ficta
|
|
|
| Diarrhea |
|
Diarrhoea
|
Diarrhea Of Presumed Infectious Origin
|
|
|
| Exudative Vitreoretinopathy 1 |
|
Retinopathy Of Prematurity
|
Retrolental Fibroplasia
|
|
EVR1
|
Criswick-Schepens Syndrome
|
|
Rop
|
Exudative Vitreoretinopathy, Familial, Autosomal Dominant
|
|
Fevr, Autosomal Dominant
|
Premature Retinopathy
|
|
Vitreoretinopathy, Exudative 1
|
Autosomal Dominant Familial Exudative Vitreoretinopathy
|
|
Fevr
|
Vitreoretinopathy, Exudative, Type 1
|
|
Retinopathy Of Prematurity Nos
|
Rlf- [Retrolental Fibroplasia]
|
|
Rop - [Retinopathy Of Prematurity]
|
Terry Syndrome
|
|
|
| Neonatal Abstinence Syndrome |
|
Drug Withdrawal Syndrome In Newborn
|
|
|
| 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]
|
|
|
| Disease By Infectious Agent |
|
Infectious Disease
|
Infectious Diseases
|
|
|
| Tobacco Addiction |
|
Nicotine Dependence
|
Tobacco Addiction, Susceptibility To
|
|
Nicotine Addiction
|
Tobacco Use Disorder
|
|
Smoking Habit
|
Nicotine Dependence, Protection Against
|
|
Nicotine Addiction, Protection From
|
Cigarette Habituation
|
|
Cigarette Habituation, Susceptibility To
|
Smoking Habit, Susceptibility To
|
|
Nicotine Dependence, Susceptibility To
|
Nicotine Addiction, Susceptibility To
|
|
Addiction, Tobacco, Susceptibility To
|
Compulsive Tobacco User Syndrome
|
|
Tobacco Dependence
|
Tobacco Dependence Syndrome
|
|
Cigarette Addiction
|
Cigarette Dependence
|
|
Smoking Addiction
|
Smokers Syndrome
|
|
|
| Anxiety |
|
Anxiety Disorder
|
Anxiety Disorders
|
|
Anxiety State
|
Anxieties
|
|
Anxiety Neurosis
|
|
|
| Invasive Aspergillosis |
|
|
| Hypertrophy Of Tongue Papillae |
|
Tongue Papillary Hypertrophy
|
Hypertrophy Of Foliate Papillae
|
|
|
| Mycobacterium Tuberculosis 1 |
|
Tuberculosis
|
Tuberculoma
|
|
Tuberculosis, Susceptibility To
|
Mycobacterium Tuberculosis, Susceptibility To, 1
|
|
Mtbs1
|
TB
|
|
|
| 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
|
|
|
| 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
|
|
|
| Conidiobolomycosis |
|
Infection By Conidiobolus
|
Rhinoentomophthoromycosis
|
|
Entomophthoromycosis Conidiobolae
|
|
|
| Epilepsy |
|
Epilepsy Syndrome
|
Epileptic Syndrome
|
|
Epilepsies
|
Symptomatic Epilepsies
|
|
Post Traumatic Epilepsy
|
Traumatic Epilepsy
|
|
Traumatic Epileptic
|
Epilepsy Due To Hippocampal Sclerosis
|
|
Epilepsy With Ammon'S Horn Sclerosis
|
Epilepsy Due To Cortical Dysplasia
|
|
Epilepsy Due To Neuronal Migration Disorders
|
|
|
| Bilirubin Metabolic Disorder |
|
Hyperbilirubinemia
|
Hereditary Hyperbilirubinemia
|
|
Hyperbilirubinemia, Hereditary
|
Hyperbilirubinaemia
|
|
|
| Major Depressive Disorder |
|
Seasonal Affective Disorder
|
Unipolar Depression
|
|
Depression
|
MDD
|
|
Depressive Disorder
|
Unipolar Depression, Susceptibility To
|
|
Major Depressive Disorder 1
|
Major Depressive Disorder, Response To Citalopram Therapy In
|
|
Major Depressive Disorder 2
|
Winter Depression
|
|
Single Major Depressive Episode
|
Sad
|
|
Clinical Depression
|
Major Depression
|
|
Depressive Syndrome
|
Major Depressive Disorder And Accelerated Response To Antidepressant Drug Treatment
|
|
Seasonal Affective Disorder, Susceptibility To
|
Recurrent Major Depression
|
|
Affective Disorder, Seasonal
|
Depression In A Seasonal Pattern
|
|
Depression
|
Seasonal
|
|
Major Depressive Disorder With A Seasonal Pattern
|
Seasonal Depression
|
|
Seasonal Mood Disorder
|
Mental Depression
|
|
Recurrent Major Depressive Episodes
|
|
|
| Acute Frontal Sinusitis |
|
|
| Outlet Dysfunction Constipation |
|
|
| Pulmonary Disease, Chronic Obstructive |
|
Chronic Obstructive Pulmonary Disease
|
COPD
|
|
Pulmonary Disease, Chronic Obstructive, Severe Early-Onset
|
Chronic Obstructive Lung Disease
|
|
Chronic Obstructive Airway Disease
|
Pulmonary Disease, Chronic Obstructive, Susceptibility To
|
|
Cold
|
Severe Early-Onset Chronic Obstructive Pulmonary Disease
|
|
Pulmonary Disease Chronic Obstructive
|
Pulmonary Disease, Obstructive, Chronic, Susceptibility To
|
|
Chronic Obstructive Pulmonary Disease Of Horses
|
Common Cold
|
|
Upper Respiratory Infections
|
Copd - [Chronic Obstructive Pulmonary Disease]
|
|
Coad - [Chronic Obstructive Airways Disease]
|
Cold - [Chronic Obstructive Lung Disease]
|
|
Chronic Airway Disease Nos
|
Chronic Airways Limitation, Unspecified
|
|
Chronic Obstructed Airway, Unspecified
|
Chronic Obstructive Airway Disease, Unspecified
|
|
Chronic Obstructive Airway, Unspecified
|
Obstructive Lung Disease Nos
|
|
Chronic Obstructive Lung Disease Nos
|
Chronic Obstructive Lung Nos
|
|
Obstructive Pulmonary Disease Nos
|
Exacerbation Copd Nos
|
|
Acute Exacerbation Copd
|
|
|
| Schizophrenia |
|
SCZD
|
Schizophrenia With Or Without An Affective Disorder
|
|
Schizophrenia 12
|
Schizophrenia, Susceptibility To
|
|
Schizophrenia-1
|
Dementia Praecox
|
|
Schizophrenia 1
|
|
|
| Rete Ovarii Benign Neoplasm |
|
|
| Rete Ovarii Adenoma |
|
|
| 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
|
|
|
| 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
|
|
|
| Lennox-Gastaut Syndrome |
|
Lennox Syndrome
|
Encephalopathy Of Childhood
|
|
Epileptic Encephalopathy Lennox-Gastaut Type
|
Childhood Epileptic Encephalopathy With Diffuse Slow Spikes And Waves
|
|
Lgs
|
|
|
| Lipoid Congenital Adrenal Hyperplasia |
|
Congenital Adrenal Hyperplasia
|
Congenital Lipoid Adrenal Hyperplasia Due To Star Deficency
|
|
Congenital Lipoid Adrenal Hyperplasia
|
Lipoid Cah
|
|
Lipoid Adrenal Hyperplasia
|
Adrenal Hyperplasia 1
|
|
Cah
|
Clah
|
|
LCAH
|
Adrenal Hyperplasia I
|
|
Lipoid Hyperplasia, Congenital, Of Adrenal Cortex With Male Pseudohermaphroditism
|
Congenital Adrenal Hyperplasia Lipoid
|
|
Adrenal Hyperplasia, Congenital
|
Congenital Adrenal Hyperplasia, Lipoid
|
|
AH1
|
Congenital Lipoid Hyperplasia Of Adrenal Cortex With Male Pseudohermaphroditism
|
|
Adrenal Hyperplasia Congenital
|
Hyperplasia, Adrenal, Lipoid, Congenital
|
|
Congenital Adrenogenital Disorders Associated With Enzyme Deficiency
|
Congenital Adrenal Cortical Hyperplasia
|
|
Congenital Adrenal Gland Hyperplasia
|
Congenital Adrenogenital Syndrome
|
|
Congenital Hyperadrenocorticism
|
Congenital Adrenogenitalism
|
|
Congenital Female Adrenal Pseudohermaphroditism
|
|
|
| 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
|
|
|
| Constipation |
|
|
| Stroke, Ischemic |
|
Cerebral Infarction
|
Stroke
|
|
Ischemic Stroke
|
Cerebrovascular Accident
|
|
Cerebral Infarction, Susceptibility To
|
Stroke, Ischemic, Susceptibility To
|
|
Cerebral Infarct
|
Ischemic Stroke, Susceptibility To
|
|
Stroke, Susceptibility To
|
Cva - Cerebral Infarction
|
|
ISCHSTR
|
Ischemic Cerebrovascular Accident
|
|
|
| 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
|
|
|
| Migraine With Or Without Aura 1 |
|
Migraine
|
Migraine With Or Without Aura, Susceptibility To, 1
|
|
Migraine Disorder
|
Migraine Variant
|
|
Migraines
|
Migraine Disorders
|
|
Mgr1
|
Mgau
|
|
Ma
|
Migraine With Or Without Aura
|
|
Classic Migraine
|
Common Migraine
|
|
Disorder, Migraine
|
Headache Migraine
|
|
Headache Migrainous
|
Migraine Headache
|
|
Migraine Syndrome
|
Headache Including Migraine
|
|
Migraine, Susceptibility To
|
|
|
| Myopathy |
|
Muscular Diseases
|
Myopathies
|
|
|
| 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
|
|
|
| Attention Deficit-Hyperactivity Disorder |
|
Attention Deficit Hyperactivity Disorder
|
ADHD
|
|
Attention Deficit Disorder
|
Attention Deficit-Hyperactivity Disorder, Susceptibility To
|
|
Attention Deficit Disorder With Hyperactivity
|
Hyperkinetic Disorder
|
|
Hyperactivity Of Childhood
|
Attention-Deficit/Hyperactivity Disorder
|
|
Add
|
Addh
|
|
Attention Deficit
|
Attention Deficit Disorder Of Childhood With Hyperactivity
|
|
Attention Deficit Disorder With Hyperactivity Syndrome
|
Hyperkinetic Syndrome
|
|
Attention-Deficit Hyperactivity Disorder
|
Attention-Deficit/Hyperactivity Disorder, Predominantly Inattentive Type
|
|
Disturbance Of Activity And Attention
|
Disorder Of Activity And Attention
|
|
Adhd - [Attention Deficit Hyperactivity Disorder]
|
Hyperkinetic Disorders
|
|
Disorder Of Activity And Attention With Hyperkinesia
|
Attention Deficit Syndrome With Hyperactivity
|
|
|
| Nervous System Disease |
|
Abnormality Of The Nervous System
|
Nervous System Diseases
|
|
Nervous System Disorder
|
|
|
