| 疾病名称 |
别名 |
|
| 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
|
|
|
| Mononeuropathy |
|
|
| Mixed Cerebral Palsy |
|
|
| Hyperthyroxinemia |
|
|
| Restrictive Cardiomyopathy |
|
Familial Restrictive Cardiomyopathy
|
Cardiomyopathy, Restrictive
|
|
Cardiomyopathy, Constrictive
|
Primary Restrictive Cardiomyopathy
|
|
Rcm
|
Cardiomyopathy Restrictive
|
|
|
| Creutzfeldt-Jakob Disease |
|
Variant Creutzfeldt-Jakob Disease
|
CJD
|
|
Bovine Spongiform Encephalopathy
|
Vcjd
|
|
Inherited Creutzfeldt-Jakob Disease
|
Creutzfeldt-Jakob Disease, Familial
|
|
Creutzfeldt Jakob Disease
|
Creutzfeldt-Jacob Disease
|
|
Creutzfeldt Jacob Disease
|
Sporadic Creutzfeldt-Jakob Disease
|
|
Encephalopathy, Bovine Spongiform
|
Creutzfeldt-Jakob Disease, Variant, Resistance To
|
|
Creutzfeldt-Jakob Disease, Variant
|
Creutzfeldt Jacob Syndrome
|
|
Jakob-Creutzfeldt Disease
|
Subacute Spongiform Encephalopathy
|
|
Transmissible Virus Dementia
|
New Variant Of Cjd
|
|
Nv-Cjd
|
Variant Cjd
|
|
Variant Creutzfeldt-Jacob Disease
|
Sporadic Cjd
|
|
Inherited Cjd
|
Acquired Creutzfeldt-Jakob Disease
|
|
Variant Mcj
|
Encephalopathy Bovine Spongiform
|
|
Familial Creutzfeldt-Jakob Disease
|
Creutzfeldt-Jakob Syndrome
|
|
New Variant Creutzfeldt-Jakob Disease
|
Creutzfeldt-Jakob Disease, Sporadic
|
|
Acquired Cjd
|
Scjd - [Sporadic Creutzfeldt-Jakob Disease]
|
|
Idiopathic Creutzfeldt-Jakob Disease
|
Creutzfeld-Jakob Disease Nos
|
|
Vcjd - [Variant Creutzfeldt-Jakob Disease]
|
|
|
| Alcoholic Neuropathy |
|
Alcoholic Polyneuropathy
|
Alcohol-Related Polyneuropathy
|
|
Alcohol-Induced Polyneuropathy
|
Alcoholic Peripheral Neuropathy
|
|
|
| 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
|
|
|
| Acute Porphyria |
|
Porphyrias, Hepatic
|
Hepatic Porphyria
|
|
Porphyria Hepatic
|
Acute Intermittent Porphyria
|
|
|
| Fundus Dystrophy |
|
Retinal Dystrophy
|
Retinal Dystrophies
|
|
Dystrophy, Retinal
|
|
|
| Middle Ear Adenocarcinoma |
|
Adenocarcinoma Of Middle Ear
|
Adenocarcinoma Of The Middle Ear
|
|
|
| Polyneuropathy |
|
|
| Arteriosclerosis |
|
Arteriosclerotic Vascular Disease
|
|
|
| Papillary Ependymoma |
|
|
| Hyperinsulinemic Hypoglycemia, Familial, 5 |
|
Hyperinsulinism Due To Insr Deficiency
|
HHF5
|
|
Familial Hyperinsulinemic Hypoglycemia 5
|
Hyperinsulinemic Hypoglycemia Due To Insr Deficiency
|
|
Hyperinsulinemic Hypoglycemia Due To Insulin Receptor Deficiency
|
Congenital Hyperinsulinism
|
|
Persistent Hyperinsulinemic Hypoglycemia Of Infancy
|
Phhi
|
|
Hyperinsulinemic Hypoglycemia Familial 5
|
|
|
| Anorexia Nervosa |
|
Anorexia Nervosa, Susceptibility To
|
ANON
|
|
Anorexia Nervosa, Susceptibility To, 1
|
An
|
|
Anorexia Nervosa 1
|
An - [Anorexia Nervosa]
|
|
|
| Arthritis |
|
Inflammatory Joint Disease
|
Inflammatory Disorder Of Joint
|
|
|
| First-Degree Atrioventricular Block |
|
First Degree Atrioventricular Block
|
First Degree Heart Block
|
|
Incomplete Atrioventricular Block, First Degree
|
First Degree Atrioventricular Heart Block
|
|
|
| Primary Cutaneous Amyloidosis |
|
Plca
|
Primary Localized Cutaneous Amyloidosis
|
|
Familial Primary Localized Cutaneous Amyloidosis
|
Amyloidosis Ix
|
|
Lichen Amyloidosis Familial
|
Amyloidosis, Primary Cutaneous
|
|
Pca
|
Amyloidosis 9
|
|
Amyloidosis Familial Cutaneous Lichen
|
Fplca
|
|
Familial Lichen Amyloidosis
|
|
|
| Nutritional Deficiency Disease |
|
Nutritional Disorder
|
Malnutrition
|
|
Nutritional Deficiency
|
Nutrition
|
|
Deficiency Diseases
|
Carbamoyl-Phosphate Synthase I Deficiency Disease
|
|
Nutrition Disorders
|
|
|
| Carpal Tunnel Syndrome |
|
Cts
|
Carpal Tunnel Syndrome, Familial
|
|
Carpal Tunnel Syndrome 1
|
CTS1
|
|
Amyotrophy, Thenar, Of Carpal Origin
|
Carpal Tunnel Median Neuropathy
|
|
Cts - Carpal Tunnel Syndrome
|
Median Nerve Entrapment
|
|
Carpal Canal
|
Carpal Tunnel
|
|
Compression Neuropathy, Carpal Tunnel
|
Distal Median Nerve Compression
|
|
Distal Median Nerve Entrapment
|
Entrapment Neuropathy, Carpal Tunnel
|
|
Median Neuropathy, Carpal Tunnel
|
Median Neuropathy Carpal Tunnel
|
|
Thenar Amyotrophy Of Crapal Origin
|
|
|
| Decubitus Ulcer |
|
Pressure Ulcer
|
Pressure Sores
|
|
Pressure Ulcers
|
Bedsore
|
|
Decubitus Ulcer
|
Decubitus Ulcer Any Site
|
|
|
| Dialysis-Related Amyloidosis |
|
Abeta2m Amyloidosis
|
Amyloidosis Beta2m
|
|
Beta2-Microglobulinic Amyloidosis
|
Variant Abeta2m Amyloidosis
|
|
Autosomal Dominant Beta2-Microglobulinic Amyloidosis
|
Aβ2m Amyloidosis
|
|
Dialysis-Related Beta2-Microglobulin Amyloidosis
|
Amyloidosis Dialysis-Related
|
|
Beta-2-Microglobulin Amyloidosis
|
Dra
|
|
Hemodialysis-Associated Amyloidosis
|
|
|
| Median Neuropathy |
|
|
| Amyloid Neuropathy |
|
Amyloid Neuropathies
|
Neuropathy Amyloid
|
|
|
| Immunoglobulin Light Chain Amyloidosis |
|
Al Amyloidosis
|
Primary Amyloidosis
|
|
Primary Systemic Amyloidosis
|
Light Chain Amyloidosis
|
|
Amyloidosis Al
|
Amyloidosis Primary Systemic
|
|
Primary Al Amyloidosis
|
Primary Systemic Al Amyloidosis
|
|
Systemic Al Amyloidsis
|
Systemic Al Amyloidosis
|
|
Light-Chain Amyloidosis
|
Alys Amyloidosis
|
|
Familial Amyloid Nephropathy Due To Lysozyme Variant
|
Familial Renal Amyloidosis Due To Lysozyme Variant
|
|
Hereditary Amyloid Nephropathy Due To Lysozyme Variant
|
Hereditary Renal Amyloidosis Due To Lysozyme Variant
|
|
Lysozyme Amyloidosis
|
Amyloidosis Primary
|
|
Immunoglobulin Deposition Disease
|
Immunoglobulinic Amyloidosis
|
|
Amyloid Al
|
|
|
| Amyloid Tumor |
|
Amyloid Neoplasm
|
Amyloid Tumour
|
|
|
| Phenylketonuria |
|
Phenylalanine Hydroxylase Deficiency
|
PKU
|
|
Pah Deficiency
|
Folling Disease
|
|
Maternal Phenylketonuria
|
Phenylketonurias
|
|
Oligophrenia Phenylpyruvica
|
Hyperphenylalaninemia, Non-Pku Mild
|
|
Folling'S Disease
|
Phenylalaninemia
|
|
Mild Phenylketonuria
|
Mild Pku
|
|
Variant Pku
|
Variant Phenylketonuria
|
|
Mpku
|
Phenylketonuria, Maternal
|
|
Deficiency Disease, Phenylalanine Hydroxylase
|
Phenylalanine Hydroxylase Deficiency Disease
|
|
Hyperphenylalaninemic Embryopathy
|
Maternal Pku
|
|
Maternal Hyperphenylalaninemia
|
Phenylketonuric Embryopathy
|
|
Hyperphenylalaninemia
|
HPA
|
|
Non-Phenylketonuria Hyperphenylalaninemia
|
NON-PKU HPA
|
|
Phenylketonuria Maternal
|
Classical Phenylketonuria
|
|
Hyperphenylalaninaemia
|
Pku - [Phenylketonuria]
|
|
|
| Obstructive Jaundice |
|
Jaundice, Obstructive
|
Cholestatic Jaundice
|
|
Cholestatic Jaundice Syndrome
|
Obstructive Hyperbilirubinemia
|
|
Jaundice Obstructive
|
Jaundice Cholestatic
|
|
|
| Analbuminemia |
|
ANALBA
|
Congenital Analbuminemia
|
|
Hypoalbuminemia
|
|
|
| Pulmonary Coin Lesion |
|
Coin Lesion Of Lung
|
Solitary Pulmonary Nodule
|
|
Coin Lesion Lung
|
|
|
| Chronic Inflammatory Demyelinating Polyradiculoneuropathy |
|
Chronic Inflammatory Demyelinating Polyneuropathy
|
Cidp
|
|
Polyradiculoneuropathy Chronic Inflammatory Demyelinating
|
Polyradiculoneuropathy, Chronic Inflammatory Demyelinating
|
|
|
| Hereditary Amyloidosis |
|
Amyloidosis Hereditary
|
Familial Amyloidosis
|
|
Amyloidosis Familial
|
Amyloidosis, Hereditary
|
|
Amyloidosis, Familial
|
Genetic Amyloidosis
|
|
Heredofamilial Amyloidosis
|
|
|
| Immunoglobulin Heavy Chain Amyloidosis |
|
Ah Amyloidosis
|
Heavy Chain Amyloidosis
|
|
Amyloidosis Derived From Immunoglobulin Heavy Chain
|
Ig Heavy-Chain-Associated Amyloidosis
|
|
|
| Gerstmann-Straussler Disease |
|
Gerstmann-Straussler-Scheinker Disease
|
Gerstmann-Straussler-Scheinker Syndrome
|
|
Prion Dementia
|
Cerebral Amyloid Angiopathy, Prnp-Related
|
|
GSD
|
Gss
|
|
Cerebellar Ataxia, Progressive Dementia, And Amyloid Deposits In Cns
|
Amyloidosis, Cerebral, With Spongiform Encephalopathy
|
|
Subacute Spongiform Encephalopathy, Gerstmann-Straussler Type
|
Encephalopathy, Subacute Spongiform, Gerstmann-Straussler Type
|
|
Amyloidosis Cerebral With Spongiform Encephalopathy
|
Cerebellar Ataxia, Progressive Dementia, And Amyloid Deposits In The Central Nervous System
|
|
Encephalopathy Subacute Spongiform Gerstmann-Straussler Type
|
Gssd
|
|
Gerstmann Straussler Scheinker Syndrome
|
Cerebral Amyloidosis With Spongiform Encephalopathy
|
|
Subacute Spongiform Encephalopathy Gerstmann-Straussler Type
|
Gluthathione Synthetase Deficiency
|
|
Gerstmann Straussler Syndrome
|
|
|
| Amyloidosis, Finnish Type |
|
Finnish Type Amyloidosis
|
Meretoja Syndrome
|
|
Amyloidosis V
|
Amyloidosis, Meretoja Type
|
|
Amyloid Cranial Neuropathy With Lattice Corneal Dystrophy
|
Lattice Corneal Dystrophy Type Ii
|
|
Familial Amyloid Polyneuropathy Type Iv
|
Amyloidosis Due To Mutant Gelsolin
|
|
Agel Amyloidosis
|
Gelsolin Amyloidosis
|
|
Familial Amyloidosis, Finnish Type
|
Hereditary Gelsolin Amyloidosis
|
|
Lattice Corneal Dystrophy Type Ii Finnish
|
Gelsolin-Related Amyloidosis
|
|
Kymenlaakso Syndrome
|
Lattice Corneal Dystrophy, Gelsolin Type
|
|
Hereditary Amyloidosis, Finnish Type
|
Lattice Corneal Dystrophy Type 2
|
|
Amyloidosis 5
|
AMYL5
|
|
Agel
|
Familial Amyloidosis Finnish Type
|
|
Meretoja Type Amyloidosis
|
Type Iv Familial Amyloid Polyneuropathy
|
|
Familial Amyloid Polyneuropathy, Type V
|
Familial Amyloid Polyneuropathy, Type Iv
|
|
|
| Contractures, Pterygia, And Spondylocarpotarsal Fusion Syndrome 1a |
|
Multiple Pterygium Syndrome, Autosomal Dominant
|
CPSFS1A
|
|
Contractures, Pterygia, And Spondylocarpostarsal Fusion Syndrome 1a
|
Autosomal Dominant Disease
|
|
Contractures, Pterygia, And Variable Skeletal Fusions Syndrome 1a
|
Cpskf1a
|
|
Pterygium Syndrome, Multiple
|
Autosomal Dominant
|
|
Arthrogryposis, Distal, Type 8, Formerly
|
Da8, Formerly
|
|
Autosomal Dominant Multiple Pterygium Syndrome
|
Distal Arthrogryposis Type 8
|
|
Arthrogryposis, Distal, Type 8
|
Da8
|
|
Pterygium Syndrome, Multiple, Autosomal Dominant
|
Autosomal Dominant Disorder
|
|
|
| Chronic Ulcer Of Skin |
|
Chronic Wounds
|
Callous Ulcer
|
|
Indolent Ulcer
|
Chronic Ulcer
|
|
|
| Amyloidosis |
|
Amyloid Disease
|
Amyloid
|
|
Amyloid Degeneration
|
Amyloidosis Nos
|
|
Amyloid Deposition
|
Amyloid Infiltration
|
|
Idiopathic Amyloidosis
|
Hyaloid Degeneration
|
|
Lardaceous Degeneration
|
|
|
| Carotenemia |
|
|
| Hypothyroidism |
|
Thyroid Diseases
|
Thyroid Deficiency
|
|
Thyroid Insufficiency
|
Dysfunction Thyroid
|
|
Thyroid Disease
|
Thyroid Dysfunction
|
|
|
| Autonomic Nervous System Disease |
|
Autonomic Nervous System Dysfunction
|
Autonomic Nervous System Disorders
|
|
Autonomic Nervous System Disorder
|
Autonomic Nervous System Diseases
|
|
Abnormality Of The Autonomic Nervous System
|
|
|
| Middle Ear Carcinoma |
|
Carcinoma Of Middle Ear
|
Carcinoma Of The Middle Ear
|
|
|
| Chronic Kidney Disease |
|
Chronic Renal Disease
|
Chronic Kidney Failure
|
|
Ckd
|
Chronic Renal Failure
|
|
Kidney Failure, Chronic
|
Chronic Renal Failure Syndrome
|
|
Crf
|
Renal Failure - Chronic
|
|
Renal Failure Chronic
|
Chronic Kidney Diseases
|
|
Chronic Kidney Disease Stage 5
|
Ckd - [Chronic Kidney Disease]
|
|
Crf - [Chronic Renal Failure]
|
Chronic Kidney Impairment
|
|
Chronic Renal Impairment
|
Chronic Kidney Shutdown
|
|
Chronic Hypoxic Kidney Failure
|
Chronic Kidney Collapse
|
|
Chronic Renal Insufficiency
|
Chronic Kidney Toxaemia
|
|
Chronic Kidney Hypofunction
|
Chronic Renal Suppression
|
|
Chronic Renal Failure, Stage 5
|
Ckd - [Chronic Kidney Disease] Stage 5
|
|
End Stage Kidney Failure
|
End Stage Renal Failure
|
|
End Stage Kidney Disease
|
End Stage Renal Disease
|
|
End Stage Chronic Renal Failure
|
Esrf - [End Stage Renal Failure]
|
|
Esrd - [End Stage Renal Diseases]
|
Egfr - [Estimated Glomerular Filtration Rate] < 15 Ml/Min/1.73m²
|
|
|
| Charcot-Marie-Tooth Disease |
|
Cmt
|
Hmsn
|
|
Hereditary Motor And Sensory Neuropathy
|
Pma
|
|
Cmt - Charcot-Marie-Tooth Disease
|
Charcot Marie Tooth Disease
|
|
Charcot-Marie-Tooth Hereditary Neuropathy
|
Charcot-Marie-Tooth Syndrome
|
|
Peroneal Muscular Atrophy
|
Hereditary Motor And Sensory Neuropathies
|
|
|
| Inclusion Body Myositis |
|
Ibm
|
Sporadic Inclusion Body Myositis
|
|
Myositis, Inclusion Body
|
Inflammatory Myopathy
|
|
Inflammatory Myopathies
|
Sibm
|
|
Myositis Inclusion Body
|
Nonaka Myopathy
|
|
Inclusion Body Myopathy, Autosomal Recessive
|
Inclusion Body Myopathy, Autosomal Dominant
|
|
Myositis
|
Inclusion Body Myopathy, Sporadic
|
|
|
| Nervous System Disease |
|
Abnormality Of The Nervous System
|
Nervous System Diseases
|
|
Nervous System Disorder
|
|
|
| Euthyroid Dysprealbuminemic Hyperthyroxinemia |
|
Euthyroid Dystransthyretinemic Hyperthyroxinemia
|
|
|
| Autonomic Neuropathy |
|
Diabetic Autonomic Neuropathy
|
|
|
| Hyperhomocysteinemia |
|
|
| 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
|
|
|
| Eunuchism |
|
|
| Diastolic Heart Failure |
|
|
| Conjunctival Deposit |
|
|
| Amyloidosis, Hereditary, Transthyretin-Related |
|
Transthyretin Amyloidosis
|
Familial Amyloid Polyneuropathy
|
|
Ttr Amyloid Neuropathy
|
Transthyretin Amyloid Neuropathy
|
|
Transthyretin Amyloid Polyneuropathy
|
Fap
|
|
Familial Transthyretin Amyloidosis
|
Amyloidosis Transthyretin Related
|
|
Type I Familial Amyloid Polyneuropathy
|
Familial Amyloid Polyneuropathy Type I
|
|
Attrv122i Amyloidosis
|
Hereditary Amyloidosis, Transthyretin-Related
|
|
Amyloid Polyneuropathy, Familial
|
Attr Amyloidosis
|
|
Attrm Amyloidosis
|
Corino De Andrade'S Disease
|
|
Paramyloidosis
|
Transthyretin-Related Hereditary Amyloidosis
|
|
Ttr Amyloidosis
|
Hereditary Attr Amyloidosis
|
|
Portuguese Polyneuritic Amyloidosis
|
Portuguese Type Familial Amyloid Neuropathy
|
|
Swiss Type Amyloid Polyneuropathy
|
Type Ii Familial Amyloid Polyneuropathy
|
|
Attrv30m Amyloidosis
|
Attrv30m-Related Amyloidosis
|
|
Familial Amyloid Polyneuropathy, Portuguese-Swedish-Japanese Type
|
Attr Cardiomyopathy
|
|
Attrv122i-Related Amyloidosis
|
Ttr-Related Amyloid Cardiomyopathy
|
|
Ttr-Related Cardiac Amyloidosis
|
Transthyretin Amyloid Cardiopathy
|
|
Transthyretin-Related Familial Amyloid Cardiomyopathy
|
Amyloidosis, Transthyretin-Related
|
|
AMYL-TTR
|
Amyloidosis I
|
|
Amyloidosis Ohio Type
|
Amyloidosis Type 7
|
|
Amyloidosis Vii
|
Amyloid Polyneuropathy
|
|
Attr
|
Familial Amyloid Polyneuropathy Type Ii
|
|
Hereditary Amyloidosis Transthyretin-Related
|
Leptomeningeal Amyloidosis
|
|
Meningocerebrovascular Amyloidosis
|
Oculoleptomeningeal Amyloidosis
|
|
Familial Amyloid Polyneuropathies
|
Amyloidosis, Leptomeningeal
|
|
Senile Cardiac Amyloidosis
|
Amyloid Neuropathies, Familial
|
|
Danish Type Familial Amyloid Cardiomyopathy
|
Familial Amyloid Neuropathy, Portuguese Type
|
|
Amyloid Polyneuropathy, Swiss Type
|
Hereditary Oculoleptomeningeal Amyloid Angiopathy
|
|
Amyloid Neuropathies
|
|
|
| Autonomic Peripheral Neuropathy |
|
Peripheral Autonomic Nervous System Diseases
|
|
|
| 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
|
|
|
| Pure Autonomic Failure |
|
Orthostatic Hypotension
|
Idiopathic Orthostatic Hypotension
|
|
Postural Hypotension
|
Bradbury-Eggleston Syndrome
|
|
Bradbury Eggleston Syndrome
|
Hypotension, Orthostatic
|
|
Hypotension, Postural
|
Paf
|
|
Pure Dysautonomia
|
Pure Idiopatic Dysautonomia
|
|
Hypotension Orthostatic
|
Primary Orthostatic Hypotension
|
|
Chronic Orthostatic Hypotension
|
|
|
| Asymmetric Motor Neuropathy |
|
|
| Amyloidosis, Familial Visceral |
|
Ostertag Type Amyloidosis
|
German Type Amyloidosis
|
|
Amyloidosis Viii
|
Amyloidosis, 3 Or More Types
|
|
Familial Visceral Amyloidosis
|
Familial Amyloid Nephropathy
|
|
Familial Renal Amyloidosis
|
Hereditary Amyloid Nephropathy
|
|
Amyloidosis, Familial Renal
|
Amyloidosis, Systemic Nonneuropathic
|
|
Amyloidosis Familial Visceral
|
Amyloidosis 8
|
|
Amyloidosis, Ostertag Type
|
Hereditary Amyloidosis With Primary Renal Involvement
|
|
Hereditary Renal Amyloidosis
|
Renal Amyloidosis
|
|
Amyloidosis, Renal
|
Systemic Nonneuropathic Amyloidosis
|
|
Amyloidosis Familial Renal
|
Amyloidosis Systemic Nonneuropathic
|
|
Hereditary Amyloidosis With Primary Renal Involement
|
AMYL8
|
|
Systemic Non-Neuropathic Amyloidosis
|
Amyloid Nephropathy
|
|
|
| Heart Valve Disease |
|
Heart Valve Diseases
|
Valvular Heart Disease
|
|
Valvular Heart Diseases
|
Heart Valve Prolapse
|
|
|
| Papilloma Of Choroid Plexus |
|
Choroid Plexus Papilloma
|
CPP
|
|
Childhood Choroid Plexus Papilloma
|
Papilloma Choroid Plexus
|
|
Papilloma, Choroid Plexus
|
Choroid Plexus Carcinoma
|
|
|
| Diabetes Mellitus |
|
|
| Hepatic Encephalopathy |
|
Encephalopathy, Hepatic
|
Portal-Systemic Encephalopathy
|
|
Hepatoencephalopathy
|
He - [Hepatic Encephalopathy]
|
|
Hepatic Encephalopathy Nos
|
Hepatic Encephalopathy, Stage Unspecified
|
|
Hepatic Coma
|
Hepatocerebral Encephalopathy
|
|
Hepatocerebral Intoxication
|
|
|
| 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
|
|
|
| Liver Cirrhosis |
|
Cirrhosis
|
Cirrhosis Of Liver
|
|
CIRRH
|
Cryptogenic Cirrhosis
|
|
Cirrhosis, Cryptogenic
|
Cirrhosis Nos
|
|
|
| Pericardial Effusion |
|
Noninflammatory Pericardial Effusion
|
Pericardium Effusion
|
|
|
| Protein-Losing Enteropathy |
|
Protein-Losing Enteropathies
|
Enteropathy, Exudative
|
|
Exudative Enteropathy
|
Ple - [Protein-Losing Enteropathy]
|
|
|
| Peripheral Nervous System Disease |
|
Peripheral Neuropathy
|
Peripheral Nerve Disease
|
|
Peripheral Nerve Disorders
|
Neuropathy, Peripheral
|
|
Peripheral Neuropathy Due To Vitamin Pyridoxine Hyperalimentation
|
|
|
| Aortic Valve Disease 2 |
|
Aortic Valve Stenosis
|
Aortic Stenosis
|
|
Rheumatic Aortic Stenosis
|
AOVD2
|
|
Bicuspid Aortic Valve
|
Rheumatic Aortic Valve Stenosis
|
|
Valvular Aortic Stenosis
|
Aortic Valve Disease, Type 2
|
|
Aortic Valve Stricture
|
Aortic Valve Obstruction
|
|
Obstructed Aorta Valve
|
Rheumatic Aortic Obstruction
|
|
Rheumatic Aortic Valve Obstruction
|
Rheumatic Aortic Stricture
|
|
Aortic Valve Regurgitation
|
Aortic Insufficiency With Stenosis
|
|
Rheumatic Aortic Valve Stenosis With Insufficiency
|
Rheumatic Aortic Stenosis With Incompetence
|
|
Rheumatic Aortic Stenosis With Regurgitation
|
|
|
| Deficiency Anemia |
|
Anemia
|
Deficiency Anemias
|
|
Anaemia
|
|
|
| Nerve Compression Syndrome |
|
Entrapment Neuropathies
|
Compression Neuropathy
|
|
Entrapment Neuropathy
|
Peripheral Nerve Entrapment Syndrome
|
|
Nerve Compression Syndromes
|
Hereditary Liability To Pressure Palsies
|
|
|
| Pineal Region Choriocarcinoma |
|
|
| Autosomal Genetic Disease |
|
Autosomal Hereditary Disorder
|
|
|
| Cataract |
|
Cataracts
|
Cat - [Cataract]
|
|
Cataract Form
|
Lens Opacity
|
|
Lens Opacities
|
|
|
| Mitral Valve Stenosis |
|
Mitral Stenosis
|
Rheumatic Mitral Stenosis
|
|
Ms - [Mitral Stenosis]
|
Mitral Valvular Stricture
|
|
Mitral Valve Stricture
|
Mitral Stricture
|
|
Chronic Mitral Stenosis
|
Mitral Obstruction
|
|
Mitral Valve Obstruction
|
Mitral Stenosis With Incompetence
|
|
Mitral Stenosis With Regurgitation
|
Rheumatic Mitral Insufficiency With Obstruction
|
|
|
| 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
|
|
|
| Choroid Plexus Cancer |
|
Choroid Plexus Carcinoma
|
Choroid Plexus Neoplasms
|
|
Choroid Plexus Neoplasm
|
Tumor Of Choroid Plexus
|
|
Tumor Of The Choroid Plexus
|
Choroid Plexus Tumor
|
|
Choroid Plexus Tumors
|
Anaplastic Choroid Plexus Papilloma
|
|
Choroid Plexus Papilloma Nos
|
Papilloma Of Choroid Plexus
|
|
Plexus Choroideus Papilloma
|
Choroid Plexus Papilloma In Fourth Ventricle
|
|
Plexus Choroideus Papilloma In Fourth Ventricle
|
|
|
| Wild-Type Amyloidosis |
|
Senile Systemic Amyloidosis
|
Attrwt Amyloidosis
|
|
Age Related Amyloidosis
|
Old Age Amyloidosis
|
|
Wild-Type Attr Amyloidosis
|
Wild-Type Transthyretin Cardiac Amyloidosis
|
|
Wild Type Attr Amyloidosis
|
Attrwt-Related Amyloidosis
|
|
Wild Type Attr-Related Amyloidosis
|
|
|
| Dysentery |
|
|
| Short Bowel Syndrome |
|
Short Gut Syndrome
|
Acquired Short Bowel Syndrome
|
|
Secondary Short Bowel Syndrome
|
Short Bowel Nos
|
|
|
| Alopecia-Mental Retardation Syndrome 1 |
|
APMR1
|
Alopecia-Intellectual Disability Syndrome 1
|
|
Amr Syndrome
|
Alopecia-Intellectual Disability Syndrome
|
|
Amr Syndrome 1
|
Alopecia With Severe Intellectual Deficit
|
|
Apmr
|
Alopecia Intellectual Disbility Syndrome 1
|
|
Perniola-Krajewska-Carnevale Syndrome
|
Alopecia - Intellectual Disability Syndrome
|
|
Alopecia With Mental Retardation Syndrome 1
|
Perniola Krajewska Carnevale Syndrome
|
|
|
| Protein-Energy Malnutrition |
|
PEM
|
Protein Energy Malnutrition
|
|
|
| Iron Metabolism Disease |
|
Iron Deficiency
|
Iron Disorder
|
|
Iron Metabolism Disorders
|
Disorder Of Iron Metabolism
|
|
Iron
|
Fe Deficiency
|
|
Iron Storage Disease
|
Iron Storage Disorder
|
|
|
| Hypervitaminosis A |
|
Hypervitaminosis A, Susceptibility To
|
Hyperalimentation Of Vitamin A
|
|
|
| Marasmus |
|
Nutritional Marasmus
|
Nutritional Atrophy
|
|
|
| Mitral Valve Disease |
|
Chronic Rheumatic Mitral Valve
|
Rheumatic Mitral Insufficiency
|
|
Disease Of Mitral Valve
|
Mitral Rh Valve Dis.
|
|
Rheumatic Disease Of Mitral Valve
|
Rheumatic Mitral Valve Changes
|
|
Rheumatic Mitral Valve Incompetence
|
Rheumatic Mitral Valve Regurgitation
|
|
Abnormality Of The Mitral Valve
|
Diseases Of Mitral Valve
|
|
Rheumatic Mitral Regurgitation
|
|
|
| Atrial Standstill 1 |
|
ATRST1
|
Atrial Cardiomyopathy With Heart Block
|
|
Cardiomyopathy, Familial, With Conduction Disturbance
|
Atrial Standstill, Digenic
|
|
Familial Cardiomyopathy With Conduction Disturbance
|
Standstill, Atrial, Type 1
|
|
Heart Block
|
Cardiomyopathies
|
|
Idiopathic Cardiomyopathy
|
Idiopathic Cardiopathy
|
|
Primary Myocardial Disease
|
Primary Cardiomyopathy
|
|
Myocardiopathy
|
Myocardosis
|
|
Primary Idiopathic Myocardial Disease
|
|
|
| Hydrocephalus |
|
Hydrocephalus, Nonsyndromic, Autosomal Recessive
|
Hydrocephalus, X-Linked
|
|
Hydrocephalus Adverse Event
|
Hydrocephaly Nos
|
|
|
| Molybdenum Cofactor Deficiency |
|
Combined Molybdoflavoprotein Enzyme Deficiency
|
Mocod
|
|
Combined Deficiency Of Sulfite Oxidase, Xanthine Dehydrogenase, And Aldehyde Oxidase
|
Combined Deficiency Of Sulfite Oxidase, Xanthine Dehydrogenase And Aldehyde Oxidase
|
|
Combined Xanthine Oxidase And Sulfite Oxidase And Aldehyde Oxidase Deficiency
|
Deficiency Of Molybdenum Cofactor
|
|
Deficiency, Molybdenum Cofactor
|
|
|
| Rheumatoid Arthritis |
|
RA
|
Arthritis, Rheumatoid
|
|
Rheumatoid Arthritis, Susceptibility To
|
Arthritis Or Polyarthritis, Rheumatic
|
|
Atrophic Arthritis
|
Rheumatism Arthritis
|
|
Rheumatoid Polyarthritis
|
|
|
| Diarrhea |
|
Diarrhoea
|
Diarrhea Of Presumed Infectious Origin
|
|
|
| Keratomalacia |
|
Vitamin A Deficiency
|
Night Blindness
|
|
Retinol Deficiency
|
Xerotic Keratitis
|
|
VAD
|
Vitamin A
|
|
Hypovitaminosis A
|
Bitot Spots
|
|
Bitot Spots In The Young Child
|
Conjunctival Xerosis With Bitot'S Spots
|
|
Vitamin A Deficiency With Cornea Xerosis
|
Vitamin A Deficiency With Cornea Ulceration Or Xerosis
|
|
|
| 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
|
|
|
| Epicardium Cancer |
|
Malignant Neoplasm Of Epicardium
|
Epicardial Tumor
|
|
Malignant Epicardial Tumor
|
Neoplasm Of Epicardium
|
|
|
| Cerebral Amyloid Angiopathy, Cst3-Related |
|
Cerebral Amyloid Angiopathy
|
Hereditary Cerebral Hemorrhage With Amyloidosis
|
|
Hchwa
|
Cerebral Amyloid Angiopathy, Familial
|
|
Hereditary Cystatin C Amyloid Angiopathy
|
Amyloidosis, Cerebroarterial, Icelandic Type
|
|
Amyloidosis Vi
|
Cerebral Hemorrhage, Hereditary, With Amyloidosis
|
|
Cst3-Related Cerebral Amyloid Angiopathy
|
Cerebral Hemorrhage, Hereditary, With Amyloidosis, Icelandic Variant
|
|
Hereditary Cerebral Hemorrhage With Amyloidosis, Icelandic Variant
|
Caa, Familial
|
|
Cerebral Amyloid Angiopathy, Genetic
|
Acys Amyloidosis
|
|
Cst3-Related Amyloidosis
|
Cystatin Amyloidosis
|
|
Hchwa, Icelandic Type
|
Hereditary Cerebral Hemorrhage With Amyloidosis, Icelandic Type
|
|
Amyloidosis 6
|
AMYL6
|
|
Acys
|
Caa
|
|
Cerebral Amyloid Angiopathy Cst3-Related
|
Cerebroarterial Amyloidosis Icelandic Type
|
|
Cystatin C Amyloidosis
|
Hccaa
|
|
Hchwai
|
Hchwa-I
|
|
Hereditary Cerebral Hemorrhage With Amyloidosis Icelandic Type
|
Cerebral Amyloid Angiopathy Familial
|
|
Angiopathy, Amyloid, Cerebral, Cst3-Related
|
Hereditary Cerebral Amyloid Angiopathy, Icelandic Type
|
|
Familial Cerebral Amyloid Angiopathy
|
Cerebral Amyloid Angiopathy, Hereditary
|
|
|
| Endocarditis |
|
|
| Demyelinating Polyneuropathy |
|
Peripheral Demyelinating Neuropathy
|
Demyelinating Peripheral Neuropathy
|
|
|
| Blepharochalasis |
|
Dermatolysis Palpebrarum
|
Adiposa Ptosis
|
|
|
| Amyotrophic Lateral Sclerosis 1 |
|
Amyotrophic Lateral Sclerosis
|
ALS
|
|
Lou Gehrig Disease
|
Amyotrophic Lateral Sclerosis Type 1
|
|
Charcot Disease
|
ALS1
|
|
Amyotrophic Lateral Sclerosis, Susceptibility To
|
Fals
|
|
Lou Gehrig'S Disease
|
Mnd
|
|
Motor Neuron Disease
|
Familial Amyotrophic Lateral Sclerosis
|
|
Amyotrophic Lateral Sclerosis 1, Familial
|
Amyotrophic Lateral Sclerosis 1, Autosomal Dominant
|
|
Motor Neuron Disease, Bulbar
|
Motor Neurone Disease
|
|
Amyotrophic Lateral Sclerosis With Dementia
|
Dementia With Amyotrophic Lateral Sclerosis
|
|
Motor Neuron Disease, Amyotrophic Lateral Sclerosis
|
Sclerosis, Lateral, Amyotrophic
|
|
Sclerosis, Lateral, Amyotrophic, Type 1
|
Amyotrophic Sclerosis
|
|
Als - [Amyotrophic Lateral Sclerosis]
|
Wasting Palsy
|
|
Amyotrophic Paralysis
|
Amyotrophy Lateral Sclerosis
|
|
Wasting Paralysis
|
Spinal Progressive Amyotrophy
|
|
Progressive Atrophic Paralysis
|
|
|
| Nephrotic Syndrome |
|
Finnish Congenital Nephrotic Syndrome
|
Ns - [Nephrotic Syndrome]
|
|
Nephrosis Syndrome
|
Nephrosis Nos
|
|
Glomerular Lesion Nephrosis
|
|
|
| Cerebrovascular Benign Neoplasm |
|
|
| Heart Conduction Disease |
|
Conduction Disorder Of The Heart
|
Heart Rhythm Disease
|
|
|
| Intraocular Pressure Quantitative Trait Locus |
|
Glaucoma
|
IOPQTL
|
|
Glaucoma, Susceptibility To
|
Postinfectious Glaucoma
|
|
Glaucoma With Ocular Inflammation
|
Glaucoma Secondary To Eye Inflammation
|
|
Traumatic Glaucoma
|
Glaucoma With Concussion Of Globe
|
|
Glaucoma Due To Ocular Trauma
|
Glaucoma Associated With Ocular Trauma
|
|
Glaucoma Secondary To Drugs
|
|
|
| Glossitis |
|
Inflammation Of Tongue
|
Tongue Inflammation
|
|
Glazed Tongue
|
|
|
| Pericardium Disease |
|
|
| Serum Amyloid A Amyloidosis |
|
Aa Amyloidosis
|
Secondary Amyloidosis
|
|
Reactive Systemic Amyloidosis
|
Apo Serum Amyloid A Amyloidosis
|
|
Inflammation Aa Amyloidosis
|
Amyloidosis Aa
|
|
Amyloid A Amyloidosis
|
Inflammatory Amyloidosis
|
|
Reactive Amyloidosis
|
Amyloidosis Secondary
|
|
Secondary Systemic Amyloidosis
|
Amyloid Aa
|
|
|
| Suppurative Uveitis |
|
|
| Cardiac Sarcoidosis |
|
|
| Barth Syndrome |
|
3-Methylglutaconic Aciduria Type 2
|
BTHS
|
|
Cardioskeletal Myopathy With Neutropenia And Abnormal Mitochondria
|
Mga Type Ii
|
|
Mga2
|
Mgca2
|
|
Mga Type 2
|
3-Methylglutaconic Aciduria Type Ii
|
|
3-Methylglutaconic Aciduria, Type Ii
|
Mga, Type Ii
|
|
3-Methylglutaconicaciduria Type 2
|
3-Methylglutaconicaciduria Type Ii
|
|
Taz Defect
|
3 Methylglutaconic Aciduria, Type Ii
|
|
Dnajc19 Defect
|
Cardioskeletal Myopathy-Neutropenia Syndrome
|
|
X-Linked Cardioskeletal Myopathy And Neutropenia
|
3-Alpha-Methylglutaconic Aciduria Type 2
|
|
Agm2
|
Cardioskeletal Myopathy-Neutropenia
|
|
Invm
|
Left Ventricular Non-Compaction Isolated X-Linked
|
|
Non-Compaction Of Left Ventricular Myocardium Isolated X-Linked
|
Agammaglobulinemia 2, Autosomal Recessive
|
|
|
| Dementia |
|
Dementias
|
Presenile Dementia
|
|
Alzheimer Type Dementia
|
Alzheimer Sclerosis
|
|
Alzheimer Disease Dementia
|
Alzheimer Dementia
|
|
Primary Degenerative Alzheimer Type Dementia
|
End Stage Alzheimer'S Dementia
|
|
Alzheimer'S Type Atypical Dementia
|
Alzheimer Type Presenile Dementia
|
|
Early Onset Alzheimer Dementia
|
Dementia In Alzheimer Disease Type 2
|
|
Dementia In Alzheimer Disease With Early Onset
|
Early Onset Alzheimer Type Dementia, Uncomplicated
|
|
Primary Degenerative Alzheimer Type Dementia, Early Onset
|
Primary Degenerative Alzheimer Type Dementia, Presenile Onset, Uncomplicated
|
|
Alzheimer Disease Dementia With Early Onset
|
Presenile Sclerosis
|
|
Presenile Brain Sclerosis
|
Presenile Alzheimer Brain Sclerosis
|
|
Late Onset Alzheimer Dementia
|
Dementia In Alzheimer Disease Type 1
|
|
Dementia In Alzheimer Disease With Late Onset
|
Primary Degenerative Alzheimer Type Dementia, Late Onset
|
|
Sdat - [Senile Dementia, Alzheimer Type]
|
Alzheimer Disease Dementia With Late Onset
|
|
Late Onset Alzheimer Brain Sclerosis
|
Senile Alzheimer Brain Disease
|
|
Senile Alzheimer Brain Sclerosis
|
Senile Primary Degenerative Alzheimer Type Dementia
|
|
Senile Dementia Of The Alzheimer Type
|
Arteriosclerotic Dementia
|
|
Strategic-Infarct Dementia
|
Post Stroke Dementia
|
|
Vascular Cognitive Impairment
|
Vascular Dementia
|
|
Dementia Of The Lewy Body Type
|
Dementia With Lewy Bodies
|
|
Sdlt - [Senile Dementia Of The Lewy Body Type]
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Senile Dementia Of The Lewy Body Type
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Alcohol-Related Dementia
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Alcoholic Dementia Nos
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Alcohol-Induced Dementia
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Alcoholic Brain Syndrome
|
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Chronic Alcoholic Brain Syndrome
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Alcohol Dementia
|
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Late Onset Alcoholic Psychosis
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Residual And Late-Onset Alcohol-Induced Psychotic Disorder
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Mental And Behavioural Disorders Due To Use Of Sedatives Or Hypnotics, Residual And Late-Onset Psychotic Disorder
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Late-Onset Psychoactive Substance-Induced Psychotic Disorder
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Inhalant Dementia
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Volatile Solvents Dementia
|
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Dementia In Paralysis Agitans
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Pdd - [Parkinson Disease Dementia]
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Dementia Syndrome Of Parkinson Disease
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Dementia In Parkinson Disease
|
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Parkinson Related Dementia
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Dementia In Huntington Chorea
|
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Hiv - [Human Immunodeficiency Virus] Dementia
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Hiv- [Human Immunodeficiency Virus] Associated Cognitive Motor Complex
|
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Hiv- [Human Immunodeficiency Virus] Associated Dementia Complex
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Aids - [Acquired Immunodeficiency Syndrome] Dementia Complex
|
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Aids Related Dementia
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Dementia Due To Niacin Deficiency
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|
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| Hypertensive Heart Disease |
|
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| Hypertrophic Cardiomyopathy |
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Hypertrophic Obstructive Cardiomyopathy
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Cardiomyopathy, Hypertrophic
|
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Cardiomyopathy, Hypertrophic, Familial
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Familial Hypertrophic Cardiomyopathy
|
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Cardiomyopathy Hypertrophic Obstructive
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Idiopathic Myocardial Hypertrophy
|
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Idiopathic Hypertrophic Cardiomyopathy
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Obstructive Idiopathic Hypertrophic Cardiomyopathy
|
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Obstructive Cardiomyopathy
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Idiopathic Hypertrophic Subaortic Stenosis
|
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Muscular Subaortic Stenosis
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Hypertrophic Obstructive Subaortic Stenosis
|
|
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| Cataract 7 |
|
Cca1
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CTRCT7
|
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Cerulean Cataract
|
Cataract 7, Cerulean Type
|
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Cataract, Congenital, Cerulean Type, 1
|
Cerulean Type Cataract 7
|
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Congenital Cerulean Type Cataract 1
|
Cataract, Congenital, Blue Dot Type 1
|
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Cataract, Congenital, Cerulean Type 1
|
Blue-Dot Cataract
|
|
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| Scoliosis |
|
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| Kidney Disease |
|
Renal Failure
|
Kidney Failure
|
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Kidney Diseases
|
Nephropathy
|
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Abnormality Of The Kidney
|
Impaired Renal Function Disease
|
|
Renal Anomaly
|
Kidney Dysfunction
|
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Renal Disease
|
Nephropathies
|
|
Renal Failure Adverse Event
|
Abnormal Renal Function
|
|
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| Pancytopenia |
|
|
| Hyperthyroxinemia, Dystransthyretinemic |
|
Dystransthyretinemic Euthyroidal Hyperthyroxinemia
|
Dystransthyretinemic Hyperthyroxinemia
|
|
DTTRH
|
Euthryroidal Hyperthyroxinemia 2
|
|
Hyperthyroxinemia, Dysprealbuminemic
|
Hyperthyroxinemia Dysprealbuminemic
|
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Hyperthyroxinemia Dystransthyretinemic
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Hyperthyroxinemia, Euthyroidal, Dystransthyretinemic
|
|
|
| Paralytic Lagophthalmos |
|
|
| Central Nervous System Disease |
|
CNS
|
Cns Diseases
|
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Central Nervous System Diseases
|
Cns Disorder
|
|
|
| Kwashiorkor |
|
Kwashiokor
|
Nutritional Edema With Dyspigmentation Of Skin And Hair
|
|
Nutritional Oedema With Dyspigmentation Of Skin And/Or Hair
|
|
|
| Constrictive Pericarditis |
|
Pericarditis, Constrictive
|
Pericarditis Constrictive
|
|
Pericarditis Calculosa
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Hutinel-Pick Syndrome
|
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Chronic Tamponade
|
Chronic Pericardial Constriction
|
|
Pick Syndrome Of Heart
|
Pick Disease Of Heart
|
|
Concretio Cordis
|
Calcareous Pericarditis
|
|
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