| 疾病名称 |
别名 |
|
| Lipoprotein Glomerulopathy |
|
|
| Hyperlipoproteinemia, Type Iii |
|
Hyperlipoproteinemia Type Iii
|
Broad-Betalipoproteinemia
|
|
Floating-Betalipoproteinemia
|
Familial Type 3 Hyperlipoproteinemia
|
|
Broad Beta Disease
|
Familial Hyperbeta- And Prebetalipoproteinemia
|
|
Familial Hypercholesterolemia With Hyperlipemia
|
Hyperlipemia With Familial Hypercholesterolemic Xanthomatosis
|
|
Coronary Artery Disease, Severe, Susceptibility To
|
Coronary Artery Disease, Severe
|
|
Hyperlipidemia Type 3
|
Familial Dysbetalipoproteinemia
|
|
Hyperlipoproteinemia Type 3
|
Coronary Artery Disease
|
|
Apolipoprotein E, Deficiency Or Defect Of
|
Dysbetalipoproteinemia Due To Defect In Apolipoprotein E-D
|
|
Carbohydrate Induced Hyperlipemia
|
Familial Hypercholesterolaemia With Hyperlipaemia
|
|
Remnant Hyperlipidemia
|
Remnant Removal Disease
|
|
Dysbetalipoproteinemia
|
Broad-Beta Disease
|
|
Familial Dyslipidemia Type 3
|
Hlp Type 3
|
|
Remnant Hyperlipoproteinemia
|
Familial Hyperlipoproteinemia Type Iii
|
|
CAD
|
Hyperlipoproteinemia 3
|
|
HLPP3
|
Deficiency Or Defect Of Apolipoprotein E
|
|
Dysbetalipoproteinemia Due To Defect In Apolipoprotein E
|
Coronary Arteriosclerosis
|
|
Coronary Heart Disease
|
|
|
| Sea-Blue Histiocyte Disease |
|
Sea-Blue Histiocytosis
|
Sea-Blue Histiocyte Syndrome
|
|
Histiocytosis, Sea-Blue
|
Inherited Lipemic Splenomegaly
|
|
SBHD
|
|
|
| Alzheimer Disease 2 |
|
AD2
|
Alzheimer Disease Associated With Apoe4
|
|
Alzheimer'S Disease 2
|
Alzheimer Disease-2
|
|
Alzheimer Disease 2, Late-Onset
|
Alzheimer Disease 2, Late Onset
|
|
Late-Onset Alzheimer Disease
|
Alzheimer Disease, Type 2
|
|
Alzheimer Disease, Late Onset
|
|
|
| Macular Degeneration, Age-Related, 1 |
|
Macular Degeneration
|
Age-Related Macular Degeneration
|
|
Macular Degeneration, Age-Related
|
Age Related Macular Degeneration
|
|
Age Related Macular Degeneration 1
|
ARMD1
|
|
Senile Macular Degeneration
|
Maculopathy, Age-Related, 1
|
|
Macular Degeneration, Age-Related, Reduced Risk Of
|
Age Related Maculopathy 1
|
|
Age Related Maculopathies
|
Age Related Maculopathy
|
|
Senile Macular Retinal Degeneration
|
Macular Degeneration Of Retina
|
|
Age-Related Maculopathy
|
Amd
|
|
Armd
|
Age-Related Maculopathy, Susceptibility To
|
|
Maculopathy Age-Related
|
Macular Degeneration, Age-Related, 1, Susceptibility To
|
|
Maculopathy, Age-Related
|
Macular Degeneration, Age-Related, Type 1
|
|
Macular Degeneration, Age-Related, 2
|
|
|
| Alzheimer Disease 3 |
|
AD3
|
Alzheimer Disease, Type 3
|
|
Alzheimer Disease, Type 3, With Spastic Paraparesis And Apraxia
|
Alzheimer Disease, Type 3, With Spastic Paraparesis And Unusual Plaques
|
|
Alzheimer'S Disease 3
|
Alzheimer Disease, Familial, 3, With Spastic Paraparesis And Apraxia
|
|
Alzheimer Disease 3, Early-Onset
|
Alzheimer Disease, Familial, 3
|
|
Alzheimer Disease, Protection Against, Due To Apoe3-Christchurch
|
Alzheimer Disease 3, Early Onset
|
|
Alzheimer Disease Familial 3
|
Early-Onset Familial Alzheimer Disease 3
|
|
Familial Alzheimer Disease 3
|
Familial Alzheimer Disease 3 With Spastic Paraparesis And Apraxia
|
|
Familial Alzheimer Disease 3 With Spastic Paraparesis And Unusual Plaques
|
Alzheimer Disease, Familial, 3, With Spastic Paraparesis And Unusual Plaques
|
|
Alzheimer Disease, Familial, Type 3
|
|
|
| Alzheimer Disease 4 |
|
AD4
|
Alzheimer Disease-4
|
|
Alzheimer'S Disease 4
|
Alzheimer Disease, Familial, 4
|
|
Alzheimer Disease, Familial4
|
Alzheimer'S Disease 4, Early Onset
|
|
Alzheimer Disease, Type 4
|
|
|
| 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]
|
Senile Dementia Of The Lewy Body Type
|
|
Alcohol-Related Dementia
|
Alcoholic Dementia Nos
|
|
Alcohol-Induced Dementia
|
Alcoholic Brain Syndrome
|
|
Chronic Alcoholic Brain Syndrome
|
Alcohol Dementia
|
|
Late Onset Alcoholic Psychosis
|
Residual And Late-Onset Alcohol-Induced Psychotic Disorder
|
|
Mental And Behavioural Disorders Due To Use Of Sedatives Or Hypnotics, Residual And Late-Onset Psychotic Disorder
|
Late-Onset Psychoactive Substance-Induced Psychotic Disorder
|
|
Inhalant Dementia
|
Volatile Solvents Dementia
|
|
Dementia In Paralysis Agitans
|
Pdd - [Parkinson Disease Dementia]
|
|
Dementia Syndrome Of Parkinson Disease
|
Dementia In Parkinson Disease
|
|
Parkinson Related Dementia
|
Dementia In Huntington Chorea
|
|
Hiv - [Human Immunodeficiency Virus] Dementia
|
Hiv- [Human Immunodeficiency Virus] Associated Cognitive Motor Complex
|
|
Hiv- [Human Immunodeficiency Virus] Associated Dementia Complex
|
Aids - [Acquired Immunodeficiency Syndrome] Dementia Complex
|
|
Aids Related Dementia
|
Dementia Due To Niacin Deficiency
|
|
|
| Familial Hyperlipidemia |
|
Familial Hyperlipoproteinemia
|
Hyperlipidaemia
|
|
Hyperlipoproteinemias
|
Hyperlipidemia
|
|
Hyperlipemia
|
Hyperlipidemias
|
|
|
| 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
|
|
|
| Vascular Dementia |
|
Dementia, Vascular
|
Multi Infarct Dementia
|
|
Multifocal Dementia
|
Dementia Vascular
|
|
Vascular Dementia, Susceptibility To
|
Dementia, Multi-Infarct
|
|
Multi-Infarct Dementia
|
|
|
| Familial Hypercholesterolemia |
|
Hyperlipoproteinemia Type Iia
|
Familial Hyperbetalipoproteinaemia
|
|
Familial Hypercholesteremia
|
Fredrickson Type Iia Hyperlipoproteinemia
|
|
Fredrickson Type Iia Lipidaemia
|
Hyperbetalipoproteinemia
|
|
Type Ii Hyperlipidemia
|
Familial Hypercholesterolæmia
|
|
Familial Hypercholesterolaemia
|
Fh
|
|
Hypercholesterolemia Familial
|
Hyperlipoproteinemia Type Ii
|
|
Hypercholesterolemia, Familial
|
|
|
| Xanthomatosis |
|
Xanthomatosis, Susceptibility To
|
Xanthelasmatosis
|
|
|
| Cerebrovascular Disease |
|
Cerebrovascular Disorder
|
Cerebrovascular Accident
|
|
Cerebrovascular Disorders
|
Cva
|
|
Stroke
|
|
|
| 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]
|
|
|
| Cerebral Amyloid Angiopathy, Cst3-Related |
|
Cerebral Amyloid Angiopathy
|
Hereditary Cerebral Hemorrhage With Amyloidosis
|
|
Hchwa
|
Hereditary Cystatin C Amyloid Angiopathy
|
|
Cerebral Amyloid Angiopathy, Familial
|
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
|
|
|
| Speech And Communication Disorders |
|
Language Disorder
|
Communication Disorder
|
|
Language Disorders
|
Communication Disorders
|
|
Speech Language Disorder
|
Speech-Language Disorder
|
|
Communication Impairment
|
Speech And Language Disorder
|
|
|
| Hyperlipoproteinemia, Type V |
|
Hyperlipoproteinemia Type V
|
Hyperchylomicronemia, Late-Onset
|
|
Familial Type 5 Hyperlipoproteinemia
|
Hyperchylomicronemia With Hyperprebetalipoproteinemia, Familial
|
|
Hyperlipidemia, Type V
|
Hyperlipemia, Mixed
|
|
Hyperlipemia, Combined Fat And Carbohydrate-Induced
|
Familial Hyperlipoproteinemia Type V
|
|
Fredrickson Type V Lipaemia
|
Hyperlipoproteinemia Type 5
|
|
Hyperchylomicronemia Late Onset
|
Hyperlipemia Combined Fat And Carbohydrate-Induced
|
|
Hyperlipemia Mixed
|
Hyperlipidemia Type V
|
|
Mixed Hyperlipemia
|
Type V Hyperlipoproteinemia
|
|
Hyperlipoproteinemia 5
|
HLPP5
|
|
Hyperlipidemia, Familial Combined
|
Mixed Hyperlipidemia
|
|
|
| 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
|
|
|
| Amyloidosis |
|
Amyloid Disease
|
Amyloid
|
|
Amyloid Degeneration
|
Amyloidosis Nos
|
|
Amyloid Deposition
|
Amyloid Infiltration
|
|
Idiopathic Amyloidosis
|
Hyaloid Degeneration
|
|
Lardaceous Degeneration
|
|
|
| Hepatitis C Virus |
|
Hepatitis C Virus, Susceptibility To
|
Hepatitis C Virus Infection, Response To Therapy Of
|
|
Hcv
|
Hcv, Susceptibility To
|
|
Hepatitis C Virus, Resistance To
|
Hepatitis C Virus, Response To Therapy Of
|
|
Resistance To Hepatitis C Virus
|
|
|
| Hepatitis C |
|
Chronic Hepatitis C
|
Hepatitis C Infection
|
|
Hepatitis Nona Nonb
|
Nanbh
|
|
Viral Hepatitis C
|
Hepatitis C Chronic
|
|
Hepatitis C, Chronic
|
Chronic Type C Viral Hepatitis
|
|
Chronic Hcv - [Hepatitis C Virus] Infection
|
Hepatitis C Nos
|
|
Hepatitis C Infection Nos
|
Hepatitis C-Related Cirrhosis
|
|
Type C Viral Hepatitis
|
Hep C Nos
|
|
|
| Subjective Cognitive Decline |
|
|
| Aortic Atherosclerosis |
|
Atherosclerosis Of Aorta
|
Aorta Atheroma
|
|
Aorta Calcification
|
Aorta Arteriosclerosis
|
|
Aortic Degeneration
|
Aortic Calcification
|
|
Aortic Atheroma
|
Aortic Arteriosclerotic Disease
|
|
Aortic Arteriosclerosis
|
Aorta Sclerosis
|
|
Aorta Degeneration
|
Atheromatous Aortic
|
|
Calcified Aortic Stenosis
|
Atheromatous Aorta
|
|
Arteriosclerotic Aortitis
|
Arteriosclerotic Aortic Stenosis
|
|
Arteriosclerotic Aorta Disease
|
Aortic Sclerosis
|
|
|
| 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
|
|
|
| Abetalipoproteinemia |
|
Acanthocytosis
|
ABL
|
|
Bassen-Kornzweig Syndrome
|
Mtp Deficiency
|
|
Familial Hypobetalipoproteinemia
|
Abetalipoproteinaemia
|
|
Microsomal Triglyceride Transfer Protein Deficiency
|
Microsomal Triglyceride Transfer Protein Deficiency Disease
|
|
Abetalipoproteinemia Neuropathy
|
Apolipoprotein B Deficiency
|
|
Bassen-Kornzweig Disease
|
Betalipoprotein Deficiency Disease
|
|
Congenital Betalipoprotein Deficiency Syndrome
|
Homozygous Familial Hypobetalipoproteinemia
|
|
Fhbl
|
Bassen Kornzweig Syndrome
|
|
Hypobetalipoproteinemia, Familial
|
Hypobetalipoproteinemia
|
|
Hypobetalipoproteinemias
|
Hypobetalipoproteinemia, Familial, Apolipoprotein B
|
|
|
| Vascular Disease |
|
Vascular Diseases
|
Aneurysm
|
|
Spinal Cord Ischemia
|
Vascular Anomaly
|
|
Spinal Cord Vascular Diseases
|
Vascular Tissue Disease
|
|
|
| Hypolipoproteinemia |
|
Hypolipoproteinaemia
|
Lipoprotein Deficiencies
|
|
Lipoprotein Disorder
|
Hypolipoproteinemias
|
|
Lipoprotein
|
Lipoprotein Deficiency
|
|
Hypolipidaemia
|
Lipoprotein Deficiency Disorder
|
|
High-Density Lipoid Deficiency
|
High-Density Lipoprotein Deficiency
|
|
Dyslipidaemia, Depressed Hdl Cholesterol
|
|
|
| Rem Sleep Behavior Disorder |
|
Rapid Eye Movement Sleep Behavior Disorder
|
Rem Sleep Behaviour Disorder
|
|
Rapid Eye Movement Sleep Behaviour Disorder
|
Rem - [Rapid Eye Movement] Behaviour Disorder
|
|
|
| Dementia, Lewy Body |
|
Lewy Body Dementia
|
Lewy Body Disease
|
|
Diffuse Lewy Body Disease
|
Dementia With Lewy Bodies
|
|
DLB
|
Autosomal Dominant Diffuse Lewy Body Disease
|
|
Cortical Lewy Body Disease
|
Dementia, Lewy Body, Susceptibility To
|
|
Lewy Body Dementia, Susceptibility To
|
Senile Dementia Of The Lewy Body Type
|
|
Dementia Of The Lewy Body Type
|
Lbd
|
|
Diffuse Lewy Body Disease With Gaze Palsy
|
Dysphasic Dementia Hereditary
|
|
Lewy Body Type Senile Dementia
|
Lewy Body Variant Of Alzheimer Disease
|
|
Lewy Bodies
|
Lewy Body
|
|
Dlbd - [Diffuse Lewy Body Disease]
|
Clbd - [Cortical Lewy Body Disease]
|
|
|
| Hepatitis |
|
Chronic Hepatitis
|
Chronic Persistent Hepatitis
|
|
Acute Hepatitis
|
Hepatitis, Chronic
|
|
Acute And Subacute Liver Necrosis
|
Acute/Subac. Necrosis Of Liver
|
|
Animal Hepatitis
|
Hepatitis Chronic
|
|
Hepatitis A
|
Hepatitis, Animal
|
|
Hepatitis Due To Toxoplasmosis
|
Hepatitis In Toxoplasmosis
|
|
Toxoplasmal Hepatitis
|
Chronic Hepatitis, Unspecified
|
|
Chronic Active Hepatitis Nec
|
Other Specified Chronic Hepatitis
|
|
Chronic Persistent Hepatitis Nec
|
Chronic Lobular Hepatitis Nec
|
|
|
| Supranuclear Palsy, Progressive, 1 |
|
Progressive Supranuclear Palsy
|
Steele-Richardson-Olszewski Syndrome
|
|
Supranuclear Palsy, Progressive
|
Progressive Supranuclear Ophthalmoplegia
|
|
Psp
|
PSNP1
|
|
Familial Progressive Supranuclear Palsy
|
Richardson'S Syndrome
|
|
Psp Syndrome
|
Progressive Supranuclear Palsy 1
|
|
Supranuclear Palsy Progressive
|
Ophthalmoplegia, Supranuclear, Progressive
|
|
Steele-Richardson-Olszewksi Syndrome
|
|
|
| Aphasia |
|
|
| Atherosclerosis Susceptibility |
|
Atherosclerosis
|
Atherosclerosis, Susceptibility To
|
|
ATHS
|
Atherogenic Lipoprotein Phenotype
|
|
Alp
|
Arteriosclerosis
|
|
|
| Carotid Stenosis |
|
Carotid Artery Stenosis
|
Stenosis, Carotid Artery
|
|
|
| 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 Amyloidosis, Finnish Type
|
Familial Amyloid Polyneuropathy Type Iv
|
|
Amyloidosis Due To Mutant Gelsolin
|
Agel Amyloidosis
|
|
Gelsolin Amyloidosis
|
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
|
|
|
| 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
|
|
|
| Splenomegaly |
|
|
| Lecithin:Cholesterol Acyltransferase Deficiency |
|
Norum Disease
|
Lcat Deficiency
|
|
Familial Lcat Deficiency
|
Fld
|
|
Lecithin Acyltransferase Deficiency
|
Complete Lcat Deficiency
|
|
Lecithin Cholesterol Acyltransferase Deficiency
|
Lecithin-Cholesterol Acyltransferase Deficiency
|
|
Familial Lecithin-Cholesterol Acyltransferase Deficiency
|
Norum'S Disease
|
|
LCATD
|
Deficiency, Lecithin:Cholesterol Acyltransferase
|
|
|
| Coronary Stenosis |
|
|
| Hypertriglyceridemia 1 |
|
Hypertriglyceridemia
|
Hypertriglyceridemia, Familial
|
|
Hypertriglyceridemia, Susceptibility To
|
HYTG1
|
|
FHTR
|
Hypertriglyceridemias Familial
|
|
|
| Smith-Lemli-Opitz Syndrome |
|
SLOS
|
Rsh Syndrome
|
|
7-Dehydrocholesterol Reductase Deficiency
|
Slo Syndrome
|
|
Rutledge Lethal Multiple Congenital Anomaly Syndrome
|
Lethal Acrodysgenital Syndrome
|
|
Polydactyly, Sex Reversal, Renal Hypoplasia, And Unilobar Lung
|
Smith-Opitz-Inborn Syndrome
|
|
Polydactyly, Sex Reversal, Renal Hypoplasia, And Unilobular Lung
|
Smith Lemli Opitz Syndrome
|
|
Smith-Lemli-Opitz Syndrome, Type Ii
|
|
|
| Kidney Disease |
|
Renal Failure
|
Kidney Failure
|
|
Kidney Diseases
|
Nephropathy
|
|
Abnormality Of The Kidney
|
Impaired Renal Function Disease
|
|
Renal Anomaly
|
Kidney Dysfunction
|
|
Renal Disease
|
Nephropathies
|
|
Renal Failure Adverse Event
|
Abnormal Renal Function
|
|
|
| Hypobetalipoproteinemia, Familial, 1 |
|
Hypobetalipoproteinemia
|
Familial Hypobetalipoproteinemia 1
|
|
Familial Hypobetalipoproteinemia
|
FHBL1
|
|
Hypobetalipoproteinemia, Familial
|
Fhbl
|
|
Acanthocytosis With Hypobetalipoproteinemia
|
Hypobetalipoproteinemias
|
|
Hypobetalipoproteinemia, Normotriglyceridemic
|
Hypo-Beta-Lipoproteinemia
|
|
Hypobetalipoprotéinemia, Familial
|
Normotriglyceridemic Hypobetalipoproteinemia
|
|
Hypobetalipoproteinemia, Familial, Type 1
|
|
|
| Hyperhomocysteinemia |
|
|
| Arteriosclerosis |
|
Arteriosclerotic Vascular Disease
|
|
|
| Sleep Apnea |
|
|
| Anosognosia |
|
|
| Anxiety |
|
Anxiety Disorder
|
Anxiety Disorders
|
|
Anxiety State
|
Anxieties
|
|
Anxiety Neurosis
|
|
|
| Inclusion Body Myositis |
|
Ibm
|
Sporadic Inclusion Body Myositis
|
|
Inflammatory Myopathy
|
Myositis, Inclusion Body
|
|
Inflammatory Myopathies
|
Sibm
|
|
Myositis Inclusion Body
|
Nonaka Myopathy
|
|
Inclusion Body Myopathy, Autosomal Recessive
|
Inclusion Body Myopathy, Autosomal Dominant
|
|
Myositis
|
Inclusion Body Myopathy, Sporadic
|
|
|
| Frontotemporal Dementia |
|
Pallidopontonigral Degeneration
|
Frontotemporal Lobar Degeneration
|
|
Semantic Dementia
|
FTD
|
|
Frontotemporal Lobe Dementia
|
Multiple System Tauopathy With Presenile Dementia
|
|
Dementia, Frontotemporal
|
Frontotemporal Dementia With Parkinsonism
|
|
Mstd
|
Frontotemporal Lobar Degeneration With Tau Inclusions
|
|
Ftld With Tau Inclusions
|
Dementia, Frontotemporal, With Parkinsonism
|
|
Fldem
|
Ftdp17
|
|
Disinhibition-Dementia-Parkinsonism-Amyotrophy Complex
|
Ddpac
|
|
Wilhelmsen-Lynch Disease
|
Wld
|
|
Ppnd
|
Dementia, Frontotemporal, With Or Without Parkinsonism
|
|
Semantic Primary Progressive Aphasia
|
Semantic Variant Ppa
|
|
Wilhemsen-Lynch Disease
|
Frontotemporal Dementia-Amyotrophic Lateral Sclerosis
|
|
Frontotemporal Dementia And Parkinsonism Linked To Chromosome 17
|
Ftd-Als
|
|
Ftld
|
Pick Complex
|
|
Pick Disease Of The Brain
|
Frontotemporal Dementia With Parkinsonism-17
|
|
Grn-Related Frontotemporal Dementia
|
Frontotemporal Dementia With Motor Neuron Disease
|
|
Dementia In Fronto-Temporal Lobar Degeneration
|
Ftd - [Frontotemporal Dementia]
|
|
Temple Dementia
|
Frontal Lobe Dementia
|
|
|
| Cardiovascular System Disease |
|
Abnormality Of The Cardiovascular System
|
Cardiovascular Disease
|
|
Disease Of Subdivision Of Hemolymphoid System
|
Disorder Of Cardiovascular System
|
|
Cardiovascular Diseases
|
|
|
| Exfoliation Syndrome |
|
Pseudoexfoliation Glaucoma
|
Pseudoexfoliation Syndrome
|
|
Exfoliation Syndrome, Susceptibility To
|
XFS
|
|
Exfoliation Glaucoma
|
Xfg
|
|
Pseudoexfoliation Of The Lens
|
Pexg
|
|
Pexs
|
Exfoliative Syndrome
|
|
Glaucoma Capsulare
|
Pex
|
|
Pseudo-Exfoliation Syndrome
|
|
|
| Hypercholesterolemia, Familial, 2 |
|
Hypercholesterolemia, Autosomal Dominant, Type B
|
FHCL2
|
|
Apolipoprotein B-100, Familial Defective
|
Apolipoprotein B-100, Familial Ligand-Defective
|
|
Hypercholesterolemia, Familial, Due To Ligand-Defective Apolipoprotein B
|
Autosomal Dominant Type B Hypercholesterolemia
|
|
Familial Ligand-Defective Apolipoprotein B-100
|
Fdb
|
|
Hypercholesterolemia, Familial, Type 2
|
Hyperlipoproteinemia Type Iib
|
|
|
| Hemorrhage, Intracerebral |
|
Intracerebral Hemorrhage
|
Hemorrhagic Stroke
|
|
ICH
|
Hemorrhage, Intracerebral, Susceptibility To
|
|
Stroke, Hemorrhagic
|
Stroke, Hemorrhagic, Susceptibility To
|
|
Brain Hemorrhage
|
|
|
| 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
|
|
|
| Mild Cognitive Impairment |
|
|
| Down Syndrome |
|
Trisomy 21
|
Complete Trisomy 21 Syndrome
|
|
Down'S Syndrome
|
Trisomy 21 Syndrome
|
|
Down'S Syndrome - Trisomy 21
|
Downs Syndrome
|
|
G Trisomy
|
47,Xx,+21
|
|
47,Xy,+21
|
Trisomy G
|
|
Down Syndrome, Susceptibility To
|
Chromosome 21 Trisomy
|
|
Trisomy 21 Nos
|
Abnormal Autosomes 21
|
|
|
| Open-Angle Glaucoma |
|
Glaucoma Simplex
|
Pigmentary Glaucoma
|
|
Wide-Angle Glaucoma
|
Glaucoma, Open-Angle
|
|
Open Angle Glaucoma
|
Glaucoma Open-Angle
|
|
Chronic Simple Glaucoma
|
Coag - [Chronic Open-Angle Glaucoma]
|
|
Csg - [Chronic Simple Glaucoma]
|
Poag - [Primary Open-Angle Glaucoma]
|
|
Oag - [Open-Angle Glaucoma]
|
Chronic Glaucoma
|
|
Chronic Open Angle Glaucoma
|
Simple Glaucoma
|
|
Chronic Noncongestive Glaucoma
|
Ltg - [Low Tension Glaucoma]
|
|
Noncongestive Glaucoma
|
Nonobstructive Glaucoma
|
|
Normal Pressure Glaucoma
|
Primary Low Tension Glaucoma
|
|
Low-Tension Glaucoma
|
Residual Stage Low Tension Glaucoma
|
|
Open Cleft Glaucoma
|
|
|
| Scrapie |
|
|
| Pick Disease Of Brain |
|
Pick Disease
|
Pick'S Disease
|
|
Pick Disease Of The Brain
|
Lobar Atrophy Of Brain
|
|
Dementia With Lobar Atrophy And Neuronal Cytoplasmic Inclusions
|
Behavioral Variant Of Frontotemporal Dementia
|
|
Dementia In Pick'S Disease
|
Lobar Atrophy Of The Brain
|
|
Bvftd
|
Bv-Ftd
|
|
PIDB
|
Picks Disease
|
|
|
| Arteriolosclerosis |
|
|
| Senile Plaque Formation |
|
|
| 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
|
|
|
| Osteoporosis |
|
Postmenopausal Osteoporosis
|
Osteoporosis, Postmenopausal
|
|
Bone Mineral Density Quantitative Trait Locus
|
Bmnd
|
|
Osteoporosis, Involutional
|
Osteoporosis, Susceptibility To
|
|
Osteoporosis, Postmenopausal, Susceptibility
|
Bone Mineral Density Variation Qtl, Osteoporosis
|
|
OSTEOP
|
Involutional Osteoporosis
|
|
Senile Osteoporosis
|
Osteoporosis Postmenopausal
|
|
Bone Mineral Density, Quantitative Trait Locus
|
Osteoporosis, Senile
|
|
Idiopathic Osteoporosis
|
Bone Rarefaction Nos
|
|
Type 1 Osteoporosis
|
|
|
| Hyperalphalipoproteinemia 1 |
|
Hyperalphalipoproteinemia
|
HALP1
|
|
Cetp Deficiency
|
Cholesterol-Ester Transfer Protein Deficiency
|
|
Familial Hyperalphalipoproteinemia
|
Cholesteryl Ester Transfer Protein Deficiency
|
|
Cept Deficiency
|
Cholesterol Ester Transfer Protein Deficiency
|
|
|
| Lipoprotein Quantitative Trait Locus |
|
Coronary Artery Disease
|
Coronary Artery Anomaly
|
|
Coronary Artery Disease, Susceptibility To
|
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
|
|
|
| Alzheimer Disease 10 |
|
Ad10
|
Alzheimer Disease-10
|
|
Alzheimer'S Disease 10
|
Alzheimer Disease, Familial, 10
|
|
Alzheimer Disease Familial 10
|
Alzheimer'S Disease 10, Early Onset
|
|
|
| Aortic Aneurysm |
|
Aortic Rupture
|
Thoracoabdominal Aortic Aneurysm, Ruptured
|
|
Ruptured Aortic Aneurysm
|
Aortic Aneurysms
|
|
Aortic Aneurysm Without Mention Of Rupture Nos
|
Ruptured Abdominal Aortic Aneurysm
|
|
Aortic Aneurysm, Ruptured
|
Ruptured Thoracic Aortic Aneurysm
|
|
|
| Neuritis |
|
|
| Simultanagnosia |
|
|
| 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
|
|
|
| Cholelithiasis |
|
|
| Herpes Zoster |
|
Shingles
|
Zoster
|
|
Herpes Zona
|
Herpes Zoster Disease
|
|
Zona Zoster
|
Herpes Zoster Of Skin And Mucous Membranes
|
|
Zoster Nos
|
Zoster With Nervous System Involvement
|
|
|
| Communicating Hydrocephalus |
|
Acquired Communicating Hydrocephalus
|
|
|
| Gerstmann Syndrome |
|
Aphasia-Angular Gyrus Syndrome
|
Developmental Gerstmann Syndrome
|
|
Gs
|
Gerstmann Badal Syndrome
|
|
Gerstmann Tetrad
|
Gerstmann'S Syndrome
|
|
Developmental Gerstmann'S Syndrome
|
|
|
| Cerebral Atherosclerosis |
|
Intracranial Arteriosclerosis
|
|
|
| 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
|
|
|
| Cerebral Amyloid Angiopathy, App-Related |
|
Hchwad
|
Amyloidosis, Cerebroarterial, App-Related
|
|
Amyloidosis, Hereditary, With Cerebral Hemorrhage, Dutch Variant
|
Cerebral Amyloid Angiopathy, App-Related, Dutch Variant
|
|
Cerebral Amyloid Angiopathy, App-Related, Iowa Variant
|
Cerebral Amyloid Angiopathy, App-Related, Italian Variant
|
|
Cerebral Amyloid Angiopathy, App-Related, Flemish Variant
|
Cerebral Amyloid Angiopathy, App-Related, Arctic Variant
|
|
Cerebral Amyloid Angiopathy, Dutch, Italian, Iowa, Flemish, Arctic Variants
|
App-Related Cerebral Amyloid Angiopathy
|
|
Abetaa21g Amyloidosis
|
Abeta Amyloidosis, Italian Type
|
|
Abeta Amyloidosis, Arctic Type
|
Abeta Amyloidosis, Iowa Type
|
|
Abeta Amyloidosis, Dutch Type
|
Hchwa-D
|
|
Abeta Amyloidosis, Flemish Type
|
Abetaa21g-Related Amyloidosis
|
|
Hchwa, Flemish Type
|
Hereditary Cerebral Hemorrhage With Amyloidosis, Flemish Type
|
|
Abetae22k Amyloidosis
|
Hchwa, Italian Type
|
|
Hereditary Cerebral Hemorrhage With Amyloidosis, Italian Type
|
Abetae22g Amyloidosis
|
|
Hchwa, Arctic Type
|
Hereditary Cerebral Hemorrhage With Amyloidosis, Arctic Type
|
|
Abetad23n Amyloidosis
|
Hchwa, Iowa Type
|
|
Hereditary Cerebral Hemorrhage With Amyloidosis, Iowa Type
|
Abetal34v Amyloidosis
|
|
Abeta Amyloidosis, Piedmont Type
|
Abetal34v-Related Amyloidosis
|
|
Hchwa, Piedmont Type
|
Hereditary Cerebral Hemorrhage With Amyloidosis, Piedmont Type
|
|
Abetae22q Amyloidosis
|
Hchwa, Dutch Type
|
|
Hereditary Cerebral Hemorrhage With Amyloidosis, Dutch Type
|
CAA-APP
|
|
Amyloidosis Cerebroarterial App-Related
|
Amyloidosis Hereditary With Cerebral Hemorrhage Dutch Variant
|
|
Cerebral Amyloid Angiopathy App-Related Arctic Variant
|
Cerebral Amyloid Angiopathy App-Related Dutch Variant
|
|
Cerebral Amyloid Angiopathy App-Related Flemish Variant
|
Cerebral Amyloid Angiopathy App-Related Iowa Variant
|
|
Cerebral Amyloid Angiopathy App-Related Italian Variant
|
Familial Occipital Calcifications With Hemorrhagic Strokes Leukoencephalopathy Arterial Dysplasia Dementia
|
|
Fochs-Ladd
|
Hereditary Cerebral Amyloid Angiopathy Dutch Type
|
|
Hereditary Cerebral Hemorrhage With Amyloidosis Dutch Type
|
Hereditary Cerebral Hemorrhage With Amyloidosis Italian Type
|
|
Cerebral Hemorrhage With Amyloidosis, Hereditary, Dutch Type
|
|
|
| Hyperuricemia |
|
Blood Urate Raized
|
Uricacidemia
|
|
|
| Binswanger'S Disease |
|
Multi-Infarct Dementia
|
Dementia Multi-Infarct
|
|
Binswanger Disease
|
|
|
| Motor Neuron Disease |
|
Anterior Horn Cell Disease
|
Motor Neuron Diseases
|
|
Mnd - [Motor Neurone Disease]
|
Lou Gehrig Disease
|
|
Creeping Palsy
|
Creeping Paralysis
|
|
Bulbar Motor Neuron Disease
|
Bulbar Syndrome
|
|
Anterior Horn Cell Disorder
|
Hereditary Motor Neuron Disease
|
|
|
| Disease Of Mental Health |
|
Mental Health
|
Mental Disorders
|
|
|
| Polycystic Lipomembranous Osteodysplasia With Sclerosing Leukoencephalopathy 1 |
|
Nasu-Hakola Disease
|
Polycystic Lipomembranous Osteodysplasia With Sclerosing Leukoencephalopathy
|
|
Plosl
|
Nhd
|
|
Presenile Dementia With Bone Cysts
|
Plo-Sl
|
|
PLOSL1
|
Dementia, Prefrontal, With Bone Cysts
|
|
Dementia, Progressive, With Lipomembranous Polycystic Osteodysplasia
|
Brain-Bone-Fat Disease
|
|
Progressive Dementia With Lipomembranous Polycystic Osteodysplasia
|
Brain-Bone-Fat Disease
|
|
|
| Machado-Joseph Disease |
|
SCA3
|
MJD
|
|
Spinocerebellar Ataxia 3
|
Azorean Disease
|
|
Spinocerebellar Ataxia Type 3
|
Spinocerebellar Atrophy
|
|
Azorean Neurologic Disease
|
Spinopontine Atrophy
|
|
Nigrospinodentatal Degeneration
|
Spinocerebellar Atrophy Iii
|
|
Spinocerebellar Atrophy Type 3
|
Azorean Ataxia
|
|
Azorean Disease Of The Nervous System
|
Machado Disease
|
|
Nigro-Spino-Dentatal Degeneration With Nuclear Ophthalmoplegia
|
Disease, Machado-Joseph
|
|
Ataxia, Spinocerebellar
|
|
|
| Hydrocephalus |
|
Hydrocephalus, Nonsyndromic, Autosomal Recessive
|
Hydrocephalus, X-Linked
|
|
Hydrocephalus Adverse Event
|
Hydrocephaly Nos
|
|
|
| Amyloidosis, Familial Visceral |
|
Ostertag Type Amyloidosis
|
German Type Amyloidosis
|
|
Familial Renal Amyloidosis
|
Amyloidosis Viii
|
|
Amyloidosis, 3 Or More Types
|
Familial Visceral Amyloidosis
|
|
Familial Amyloid Nephropathy
|
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
|
|
|
| Optic Neuritis |
|
Inflammatory Optic Neuropathy
|
|
|
| Generalized Atherosclerosis |
|
Generalised Atherosclerosis
|
|
|
| Urolithiasis |
|
|
| Carotid Artery Disease |
|
Carotid Artery Diseases
|
Disorder Of Carotid Artery
|
|
|
| Basal Ganglia Cerebrovascular Disease |
|
|
| Visual Agnosia |
|
|
| Temporal Lobe Epilepsy |
|
Epilepsy, Temporal Lobe
|
Epilepsy Temporal Lobe
|
|
|
| Nephrotic Syndrome |
|
Finnish Congenital Nephrotic Syndrome
|
Ns - [Nephrotic Syndrome]
|
|
Nephrosis Syndrome
|
Nephrosis Nos
|
|
Glomerular Lesion Nephrosis
|
|
|
| Alexia |
|
Dyslexia
|
Dyslexia, Acquired
|
|
Acquired Dyslexia
|
Aphemesthaesia
|
|
|
| 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
|
|
|
| Coronary Heart Disease 1 |
|
Coronary Heart Disease
|
Coronary Heart Disease, Susceptibility To, 1
|
|
Chds1
|
Coronary Heart Disease, Susceptibility To
|
|
CHD
|
Heart, Coronary, Disease, Susceptibility To, Type 1
|
|
Coronary Arteriosclerosis
|
Coronary Artery Disease
|
|
|
| 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
|
|
|
| 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
|
|
|
| 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
|
|
|
| Hypercholesterolemia, Familial, 1 |
|
Hypercholesterolemia
|
FHCL1
|
|
Fhc
|
Fh
|
|
Hyperlipoproteinemia, Type Ii
|
Hyperlipoproteinemia, Type Iia
|
|
Hyper-Low-Density-Lipoproteinemia
|
Hypercholesterolemic Xanthomatosis, Familial
|
|
Ldl Receptor Disorder
|
Hypercholesterolemia, Susceptibility To
|
|
Hypercholesterolemia, Familial, Modifier Of
|
Hypercholesterolemia, Familial, Due To Ldlr Defect, Modifier Of
|
|
Ldl Cholesterol Level Qtl2
|
Hyperlipoproteinemia Type Ii
|
|
Hypercholesterolemia, Familial, Type 1
|
High Cholesterol
|
|
Increased Cholesterol
|
Low-Density-Lipoid-Type Hyperlipoproteinemia
|
|
Pure Hypercholesterolaemia
|
Ldl - [Low Density Lipoprotein} Hyperlipoproteinemia
|
|
Group A Hyperlipidaemia
|
Pure Hypercholesterinaemia
|
|
Cholesterolaemia
|
Essential Cholesterolaemia
|
|
Essential Hypercholesterolaemia
|
Group A Hyperlipemia
|
|
Increased Low Density Lipoprotein
|
Low-Density-Lipoprotein-Type
|
|
Low-Density-Lipoprotein-Type Hyperlipoproteinemia
|
|
|
| Acquired Immunodeficiency Syndrome |
|
Acquired Immune Deficiency Syndrome
|
AIDS
|
|
Acquired Immune Deficiency
|
Acquired Immunodeficiency
|
|
Acquired Immunodeficiency Due To Protein Loss
|
|
|
| Sucrase-Isomaltase Deficiency, Congenital |
|
Congenital Sucrase-Isomaltase Deficiency
|
CSID
|
|
Si Deficiency
|
Congenital Sucrose Intolerance
|
|
Disaccharide Intolerance
|
Sucrase-Isomaltase Deficiency
|
|
Disaccharide Intolerance I
|
Congenital Sucrose-Isomaltose Malabsorption
|
|
Sucrose-Isomaltose Malabsorption, Congenital
|
Sucrose Intolerance, Congenital
|
|
Congenital Sucrase-Isomaltose Malabsorption
|
Congenital Sucrose-Isomaltase Malabsorption
|
|
Disaccharide Intolerance, 1
|
Sucrose Intolerance Congenital
|
|
Sucrose-Isomaltase Malabsorption, Congenital
|
Disaccharidase Deficiency
|
|
Invertase Deficiency
|
Sucrase-Alpha-Dextrinase Deficiency
|
|
Disaccharide Intolerance Type I
|
Csid - [Congenital Sucrase-Isomaltase Deficiency]
|
|
Sucrose Intolerance Of Newborn
|
Sucrose Intolerance
|
|
Sucrase Deficiency
|
Disaccharide Malabsorption
|
|
Intestinal Disaccharidase Deficiency
|
|
|
| Normal Pressure Hydrocephalus |
|
Low Pressure Hydrocephalus
|
Hydrocephalus Normal Pressure
|
|
Hydrocephalus, Normal Pressure
|
Normal Pressure Hydrocephalus Nos
|
|
Nph - [Normal Pressure Hydrocephalus]
|
Normal Pressure Hydrocephaly
|
|
|
| Cerebral Palsy |
|
Infantile Cerebral Palsy
|
Mixed Cerebral Palsy
|
|
Palsy Cerebral
|
Palsy, Cerebral
|
|
Cerebral Palsy, Mixed
|
|
|
| Female Breast Nipple And Areola Cancer |
|
Malignant Neoplasm Of Nipple And Areola Of Female Breast
|
Malignant Neoplasm Of Nipple Or Areola Of Female Breast
|
|
|
| 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
|
|
|
| Chromosomal Duplication Syndrome |
|
|
| Amnestic Disorder |
|
Amnesia
|
Amnestic Syndrome
|
|
Korsakoff'S Psychosis Or Syndrome
|
Amnesic Syndrome
|
|
Amnestic Disorder In Conditions Classified Elsewhere
|
Korsakoff Psychosis Or Syndrome, Nonalcoholic
|
|
Nonalcoholic Organic Amnesic Syndrome
|
Organic Amnesic Syndrome
|
|
|
| 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
|
|
|
| Aortic Disease |
|
Aortic Diseases
|
Aortic Disorder
|
|
Disorder Of The Aorta
|
|
|
| Arcus Corneae |
|
Arcus Senilis
|
Corneal Arcus
|
|
Arcus Of Cornea
|
|
|
| Autoimmune Atherosclerosis |
|
|
| Obsessive-Compulsive Disorder |
|
OCD
|
Obsessive-Compulsive Disorder, Susceptibility To
|
|
Anancastic Neurosis
|
Obsessive Compulsive Disorder
|
|
Anankastic Neurosis
|
Obsessive-Compulsive Neurosis
|
|
Obsessive Compulsive Behavior
|
|
|
| Nonobstructive Coronary Artery Disease |
|
Non-Cad
|
Non-Obstructive Coronary Artery Disease
|
|
|
| Parkinsonism |
|
Parkinsonism-Plus
|
Idiopathic Parkinsonism
|
|
Primary Parkinsonism
|
Paralysis Agitans Syndrome
|
|
Parkinsonian Syndrome
|
Trembling Paralysis
|
|
Paralysis Agitans
|
Shaking Palsy
|
|
Shaking Paralysis
|
|
|
| Nominal Aphasia |
|
|
| Hyperlipoproteinemia, Type Iv |
|
Hyperlipoproteinemia Type Iv
|
Carbohydrate-Inducible Hyperlipemia
|
|
Endogenous Hyperlipidaemia
|
Familial Hypertriglyceridemia
|
|
Fredrickson Type Iv Hyperlipoproteinemia
|
Fredrickson Type Iv Lipidaemia
|
|
Fredrickson Type Iv Lipidemia
|
Vldl Hyperlipoproteinemia
|
|
Hyperlipoproteinemia Type 4
|
Carbohydrate Inducible Hyperlipemia
|
|
Familial Type Iv Hyperlipoproteinemia
|
Familial Hyperlipoproteinemia Type Iv
|
|
|
| Familial Lipoprotein Lipase Deficiency |
|
Familial Lpl Deficiency
|
Familial Hyperchylomicronemia
|
|
Hyperlipoproteinemia Type I
|
Familial Hyperlipoproteinemia Type I
|
|
Hyperchylomicronemia
|
Burger-Grutz Syndrome
|
|
Endogenous Hypertriglyceridaemia
|
Familial Fat-Induced Hypertriglyceridemia
|
|
Lipd Deficiency
|
Lpl Deficiency
|
|
Lipase D Deficiency
|
Lipoprotein Lipase Deficiency, Familial
|
|
Familial Chylomicronemia Syndrome
|
Fredrickson Type I Hyperlipoproteinemia
|
|
Fredrickson Type I Lipaemia
|
Hypercholesterinaemic Xanthomatosis
|
|
Mixed Hyperglyceridemia
|
Lipoprotein Lipase Deficiency
|
|
Type I Hyperlipoproteinemia
|
Hyperlipoproteinemia Type Ia
|
|
Familial Hyperlipo-Proteinemia Type 1
|
|
|
| Beta-Thalassemia |
|
Beta Thalassemia
|
Cooley'S Anemia
|
|
Mediterranean Anemia
|
Beta Thalassemia Intermedia
|
|
Erythroblastic Anemia
|
Thalassemia, Hispanic Gamma-Delta-Beta
|
|
Thalassemia Major
|
Thalassemia Minor
|
|
Beta-Plus-Thalassemia
|
Thalassemia, Beta
|
|
Beta Thalassemia Major
|
Beta Thalassemia Minor
|
|
Thalassemias, Beta-
|
Microcytemia, Beta Type
|
|
Thalassemia, Beta Type
|
B-THAL
|
|
Mediterranean Anaemia
|
Beta Thalassaemia Syndrome
|
|
Mediterranean Disease
|
Beta Thalassaemia Disease
|
|
|
| Anterograde Amnesia |
|
|
| Siderosis |
|
Pulmonary Siderosis
|
Deposition Of Iron
|
|
Arc-Welders' Disease
|
Arc-Welders' Lung
|
|
Arc-Welders' Nodulation
|
Arc-Welders' Pneumoconiosis
|
|
Iron Oxide Lung
|
Iron Pneumoconiosis
|
|
Pneumoconiosis Siderotico
|
Siderotic Lung Disease
|
|
Steel Grinders' Disease
|
Welders' Lung
|
|
Welders' Siderosis
|
Lung Fibrosis With Siderosis
|
|
|
| Tetralogy Of Fallot |
|
TOF
|
Fallot Tetralogy
|
|
Ventricular Septal Defect With Pulmonary Stenosis Or Atresia, Dextraposition Of Aorta, And Hypertrophy Of Right Ventricle
|
Tetrad Of Fallot
|
|
Fallot Tetrad
|
Fallot Disease
|
|
Fallot Complex
|
Subpulmonic Stenosis, Ventricular Septal Defect, Overriding Aorta, And Right Ventricular Hypertrophy
|
|
Interventricular Septal Defect With Dextroposition Of Aorta, Pulmonary Stenosis And Hypertrophy Of Right Ventricle
|
Interventricular Septal Defect, In Tetralogy Of Fallot
|
|
Ventricular Septal Defect With Obstructed Right Ventricular Outflow
|
Tof - [Tetralogy Of Fallot]
|
|
Pulmonary Atresia With Ventricular Septal Defect [Fallot Type]
|
Pulmonary Atresia, Ventricular Septal Defect And Mapcas
|
|
Pulmonary Atresia With Ventricular Septal Defect And Systemic-To-Pulmonary Collateral Arteries [Fallot Type]
|
|
|
| Hyperlipoproteinemia, Type I |
|
Lipoprotein Lipase Deficiency
|
Familial Chylomicronemia Syndrome
|
|
Lpl Deficiency
|
Hyperchylomicronemia, Familial
|
|
Hyperlipemia, Idiopathic, Burger-Grutz Type
|
Hyperlipemia, Essential Familial
|
|
Lipase D Deficiency
|
Lipd Deficiency
|
|
Hyperlipoproteinemia, Type Ia
|
Chylomicronemia, Familial
|
|
High Density Lipoprotein Cholesterol Level Qtl 11
|
Hyperlipoproteinemia Type 1
|
|
Hyperlipoproteinemia 1
|
HLPP1
|
|
Lipoprotein Lipase
|
Hyperlipoproteinemia Type I
|
|
Familial Hyperchylomicronemia Syndrome
|
|
|
| Type 1 Diabetes Mellitus |
|
Diabetes Mellitus, Insulin-Dependent
|
Diabetes Mellitus Type 1
|
|
IDDM
|
Type 1 Diabetes
|
|
Insulin-Dependent Diabetes Mellitus
|
T1D
|
|
Juvenile-Onset Diabetes
|
Jod
|
|
Diabetes Mellitus, Type 1
|
Diabetes Mellitus, Insulin-Dependent-1
|
|
Type I Diabetes Mellitus
|
Autoimmune Diabetes
|
|
Juvenile Diabetes
|
Juvenile-Onset Diabetes Mellitus
|
|
Diabetes, Insulin Dependent
|
Insulin-Dependent Diabetes Mellitus-1
|
|
Diabetes Mellitus Insulin-Dependent
|
Diabetes Autoimmune
|
|
Diabetes Mellitus, Insulin-Dependent, Susceptibility To
|
Diabetes Mellitus, Type 1, Susceptibility To
|
|
Diabetes Type 1
|
Type I Diabetes
|
|
Diabetes, Autoimmune
|
T1dm - [Type 1 Diabetes Mellitus]
|
|
Iddm - [Insulin Dependent Diabetes Mellitus]
|
Type 1 Iddm
|
|
Juvenile Diabetes Mellitus Without Compications
|
Idiopathic Insulin-Dependent Diabetes Mellitus Without Complications
|
|
Juvenile-Onset Diabetes Mellitus Without Compications
|
Ketosis-Prone Diabetes Mellitus Without Compications
|
|
Juvenile-Onset-Type Diabetes Mellitus Without Compications
|
|
|
| Aortic Aneurysm, Familial Abdominal, 1 |
|
Abdominal Aortic Aneurysm
|
Aortic Aneurysm, Familial Abdominal 1
|
|
Aneurysm, Abdominal Aortic
|
AAA
|
|
Aortic Aneurysm, Abdominal
|
AAA1
|
|
Aortic Aneurysm, Familial Abdominal
|
Aortic Aneurysm Abdominal
|
|
Abdominal Aortic Aneurysms
|
Abdominal Aortic Aneurysm Without Mention Of Perforation Or Rupture
|
|
Abdomen Aneurysm
|
Abdominal Aorta Aneurysm
|
|
Aneurysm Of Abdominal Aorta
|
Aortic Abdomen Aneurysm
|
|
Aaa - [Abdominal Aortic Aneurysm]
|
Abdominal Aneurysm
|
|
Abdominal Aorta Aneurysm Rupture
|
Abdominal Aorta Aneurysm Ruptured
|
|
Abdominal Aortic Aneurysm Which Has Ruptured
|
Ruptured Aaa
|
|
Abdomen Aorta Aneurysm Ruptured
|
Abdomen Aorta Rupture
|
|
Abdomen Aortic Aneurysm Rupture
|
Abdomen Aneurysm Rupture
|
|
Abdomen Aortic Aneurysm Ruptured
|
Abdomen Aortic Rupture
|
|
Abdominal Aorta Rupture
|
Abdominal Aortic Rupture
|
|
Rupture Abdomen Aorta Aneurysm
|
Rupture Abdominal Aortic Aneurysm
|
|
Ruptured Abdomen Aneurysm
|
Ruptured Abdomen Aorta
|
|
Ruptured Abdomen Aortic
|
Ruptured Abdominal Aneurysm
|
|
Ruptured Abdominal Aorta
|
Ruptured Abdominal Aortic
|
|
Ruptured Aorta Abdominalis Aneurysm
|
False Abdomen Aorta Aneurysm Ruptured
|
|
False Abdominal Aortic Aneurysm Ruptured
|
False Abdominal Aorta Aneurysm Ruptured
|
|
False Abdomen Aortic Aneurysm Ruptured
|
|
|
| Ideomotor Apraxia |
|
Apraxia, Ideomotor
|
Classic Apraxia
|
|
Ideomotor Dyspraxia
|
Limb-Kinetic Apraxia
|
|
Transcortical Apraxia
|
|
|
| Peripheral Artery Disease |
|
Peripheral Arterial Disease
|
Peripheral Arterial Diseases
|
|
|
| Arteries, Anomalies Of |
|
Artery Disease
|
Arteriopathic Disease
|
|
|
| Apnea, Obstructive Sleep |
|
Obstructive Sleep Apnea Syndrome
|
Obstructive Sleep Apnea
|
|
Sleep Apnea, Obstructive
|
Osa
|
|
Osas
|
Sleep Apnea/Hypopnea Syndrome
|
|
Sahs
|
Upper Airway Resistance Sleep Apnea Syndrome
|
|
Apnea, Obstructive
|
Obstructive Apnea
|
|
Osahs
|
Sleep Apnea Hypopnea Syndrome
|
|
Sleep Apnea Syndrome, Obstructive
|
Sleep Apnea Obstructive
|
|
Sleep Apnea Syndromes
|
Obstructive Sleep Apnoea Syndrome
|
|
Obstructive Sleep Apnoea, Adult
|
Osa - [Obstructive Sleep Apnoea]
|
|
Obstructive Sleep Apnoea, Paediatric
|
Obstructive Sleep Apnoea Hypopnoea Syndrome
|
|
Osa Syndrome
|
Sleep Apnoea Nos
|
|
[Sas] - Sleep Apnoea Syndrome
|
Sleep Apnoea Syndrome
|
|
[Osahs] - Obstructive Sleep Apnoea-Hypopnea Syndrome
|
[Sahs] - Sleep Apnoea-Hypopnea Syndrome
|
|
|
| Rett Syndrome |
|
Atypical Rett Syndrome
|
RTT
|
|
Rett Disorder
|
Rts
|
|
Autism, Dementia, Ataxia, And Loss Of Purposeful Hand Use
|
Rett Syndrome, Preserved Speech Variant
|
|
Rett Syndrome, Atypical
|
Rett'S Disorder
|
|
Rett Syndrome Variant
|
Autism-Dementia-Ataxia-Loss Of Purposeful Hand Use Syndrome
|
|
Cerebroatrophic Hyperammonemia
|
Rett Like Syndrome
|
|
Rett'S Syndrome
|
Atypical Rtt
|
|
Autism-Dementia-Ataxia-Loss Of Purposeful Hand Use
|
Rett Syndrome Preserved Speech Variant
|
|
Rett Syndrome Zappella Variant
|
Rett Syndrome, Zappella Variant
|
|
|
| Hypoalphalipoproteinemia, Primary, 1 |
|
Familial Hdl Deficiency
|
Fha
|
|
High Density Lipoprotein Deficiency
|
Familial Hypoalphalipoproteinemia
|
|
Hypoalphalipoproteinemia, Familial
|
Hdld
|
|
Fhd
|
Hdl Deficiency, Type 2
|
|
Primary Hypoalphalipoproteinemia 1
|
Hdl Cholesterol, Low Serum
|
|
Hdlc
|
Hdl Deficiency, Familial, 1
|
|
Hypoalphalipoproteinemia, Primary
|
Low Serum Hdl Cholesterol
|
|
Primary Hypoalphalipoproteinemia
|
FHA1
|
|
Hdld2
|
High Density Lipoprotein Deficiency 2
|
|
Hypoalphalipoproteinemias
|
Apolipoprotein A-I Deficiency
|
|
|
| Hypothyroidism |
|
Thyroid Diseases
|
Thyroid Disease
|
|
Thyroid Deficiency
|
Thyroid Insufficiency
|
|
Dysfunction Thyroid
|
Thyroid Dysfunction
|
|
|
| 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
|
|
|
| Sitosterolemia |
|
Phytosterolemia
|
Beta-Sitosterolemia
|
|
Plant Sterol Storage Disease
|
Phytosterolæmia
|
|
Sitosterolæmia
|
Retention Of Dietary Cholesterol And Abnormal Retention Of Non-Cholesterol Sterols In The Body
|
|
Phytosterolaemia
|
Sitosterolaemia
|
|
Sitosterolemia With Xanthomatosis
|
|
|
| Degeneration Of Macula And Posterior Pole |
|
Degeneration Of Macula And Posterior Pole Of Retina
|
Degeneration Of Macula Or Posterior Pole
|
|
Macular Degeneration Nos
|
Degenerative Disorder Of Macula
|
|
Drusen Macular Degeneration
|
Posterior Pole Macular Degeneration Of Eye
|
|
Macular Eye Degeneration
|
Macular Degeneration Of Retina, Unspecified
|
|
Pseudohole Degeneration Of Macula Of Retina
|
|
|
| Residual Stage Of Open Angle Glaucoma |
|
Open-Angle Glaucoma Residual Stage
|
|
|
| Holoprosencephaly |
|
Holoprosencephaly Sequence
|
Hpe
|
|
Hpe - [Holoprosencephaly]
|
|
|
| Abcd Syndrome |
|
ABCDS
|
Albinism, Black Lock, Cell Migration Disorder Of The Neurocytes Of The Gut, And Deafness
|
|
Albinism, Black Lock, Cell Migration Disorder Of The Neurocytes Of The Gut And Deafness
|
|
|
| Malaria |
|
Malaria, Susceptibility To
|
Malaria, Resistance To
|
|
Malaria, Cerebral
|
Cerebral Malaria
|
|
Malaria, Severe, Susceptibility To
|
Malaria, Severe, Resistance To
|
|
Malaria, Cerebral, Susceptibility To
|
Induced Malaria
|
|
Malaria, Vivax, Protection Against
|
Malaria, Severe
|
|
Malaria, Cerebral, Reduced Risk Of
|
Malaria, Protection Against
|
|
Resistance To Malaria Due To G6pd Deficiency
|
Malaria Due To G6pd Deficiency
|
|
Malarial Encephalitis
|
CM
|
|
Malaria Cerebral
|
Susceptibility To Malaria
|
|
Acute Pernicious Fever
|
Aestivo-Autumnal Fever
|
|
Aestivo Autumnal Malaria
|
Chagres Fever
|
|
Continued Malaria Fever
|
Estivo-Autumnal Fever
|
|
Estivo-Autumnal Malaria
|
Estivo-Autumnal Malarial Fever
|
|
Falciparum Fever
|
Malignant Tertian Fever
|
|
Malignant Tertian Malaria
|
Pernicious Intermittent Fever
|
|
Pernicious Malaria
|
Quotidian Malaria
|
|
Subtertian Fever
|
Subtertian Malaria Fever
|
|
Subtertian Malignant Tertian Malaria
|
Tropical Malaria
|
|
Algid Malaria
|
Bilious Haemoglobinuric Fever
|
|
Black Water Fever
|
Blackwater Fever
|
|
Malarial Blackwater Fever
|
Severe Malarial Falciparum
|
|
West African Fever
|
Malarial Haematinuria
|
|
Haemoglobinuric Fever
|
Haemoglobinuric Malaria
|
|
Severe Plasmodium Falciparum Malaria
|
Malarial Haemoglobinuria
|
|
Malarial Haematuria
|
Falciparum Malaria [Malignant Tertian]
|
|
Malaria Tropica
|
Malarial Shock
|
|
Chagres Virus Disease
|
Malignant Malaria
|
|
Mtm - [Malignant Tertian Malaria]
|
Tm -[Malignant Tertian Malaria]
|
|
Panama Fever
|
St - [Subtertian Malaria]
|
|
Malarial Quotidian
|
Benign Tertian Malaria
|
|
Tertian Ague
|
Vivax Fever
|
|
Plasmodium Vivax Malaria Nos
|
Btm - [Benign Tertian Malaria]
|
|
Bt - [Benign Tertian Malaria]
|
Vivax Malaria
|
|
Benign Tertian Vivax Malaria
|
Tertian Malaria
|
|
Quartan Malaria
|
Quartan Ague
|
|
Quartan Fever
|
Plasmodium Malariae Malaria Nos
|
|
Quartan Malarial
|
Malaria By Plasmodium Malariae
|
|
Malariae Malaria
|
Ovale Tertian Malaria
|
|
Plasmodium Ovale Fever
|
Malaria Fever By Plasmodium Ovale
|
|
Ovale Malaria
|
Malaria By Plasmodium Ovale
|
|
Malarial Ovale
|
Marsh Fever
|
|
Remittent Congestive Fever
|
Coastal Fever
|
|
Remittent Gastric Fever
|
Miasmatic Fever
|
|
Congestive Remittent Fever
|
Intermittent Fever
|
|
Jungle Fever
|
Paludism
|
|
Cameroon Fever
|
Ague
|
|
Corsican Fever
|
Intermittent Bilious Fever
|
|
Disease Due To Plasmodiidae
|
Malarial Fever
|
|
Plasmodiosis
|
Remittent Fever
|
|
Roman Fever
|
Malaria Fever Nos
|
|
Malaria Nos
|
Paludal Fever
|
|
Clinically Diagnosed Malaria
|
Clinically Diagnosed Malaria Without Parasitological Confirmation
|
|
Congestive Fever
|
Malarial Cachexia
|
|
Marsh Cachexia
|
Paludal Cachexia
|
|
Recurrent Malaria
|
Remittent Malaria
|
|
|
| Aortic Dissection |
|
|
| Narcolepsy |
|
Paroxysmal Sleep
|
Gelineau Syndrome
|
|
Narcoleptic Syndrome
|
Narcolepsy-Cataplexy Syndrome
|
|
Cataplexy And Narcolepsy
|
Narcolepsy, Without Cataplexy
|
|
Gelineau'S Syndrome
|
Narcolepsy With Or Without Cataplexy
|
|
Narcolepsy Nos
|
|
|
| Cerebral Degeneration |
|
Brain Degeneration
|
Degenerative Brain Disorder
|
|
|
| Agraphia |
|
|
| Transient Cerebral Ischemia |
|
Transient Ischemic Attack
|
Transient Ischemic Attacks
|
|
Tia
|
Tia - Transient Ischaemic Attack
|
|
Transient Cerebral Ischaemia
|
Ischemic Attack, Transient
|
|
Intermittent Cerebral Ischemia
|
Tia - [Transient Ischaemic Attack]
|
|
Intermittent Cerebral Ischaemia
|
Transient Cerebral Ischaemic Attack, Unspecified, Course Of Resolution Unspecified
|
|
|
| Diabetes Mellitus |
|
|
| Ovarian Cancer |
|
Ovarian Carcinoma
|
Ovarian Neoplasm
|
|
Malignant Tumour Of Ovary
|
Cancer Of The Ovary
|
|
Epithelial Ovarian Cancer
|
Neoplasm Of Ovary
|
|
Ovarian Neoplasms
|
Ovarian Cancers
|
|
Malignant Neoplasm Of Ovary
|
Primary Malignant Neoplasm Of Ovary
|
|
Ovarian Cancer, Somatic
|
Malignant Ovarian Tumor
|
|
Ovary Neoplasm
|
Primary Ovarian Cancer
|
|
Tumor Of The Ovary
|
Malignant Neoplasm Of The Ovary
|
|
Malignant Tumor Of The Ovary
|
Ovarian Malignant Tumor
|
|
OC
|
Ovarian Carcinomas
|
|
Cancer, Ovarian
|
Cancer Of Ovary
|
|
Ovary Cancer
|
Ca Ovary
|
|
|
| Diabetic Angiopathy |
|
Diabetic Angiopathies
|
Diabetic Peripheral Angiopathy
|
|
Diabetic Vascular Disorder
|
|
|
| Intracranial Embolism |
|
Cerebral Embolism
|
Cerebral Embolism With Cerebral Infarction
|
|
|
| Bipolar Disorder |
|
Bipolar Depression
|
Manic Disorder
|
|
Depression, Bipolar
|
Bipolar Disorder Manic Phase
|
|
Depressive-Manic Psych.
|
Manic Bipolar Affective Disorder
|
|
Manic Bipolar I Disorder
|
Manic Depression
|
|
Manic Depressive Disorder
|
Mixed Bipolar Disorder
|
|
Bipolar Affective Disorder
|
Bipolar Affective Psychosis
|
|
Bipolar Spectrum Disorder
|
Manic Depressive Illness
|
|
Depression Bipolar
|
Bipolar Disorder, Mixed
|
|
Major Affective Disorder
|
Major Affective Disorder 1
|
|
Major Affective Disorder 2
|
|
|
| Toxic Encephalopathy |
|
Neurotoxicity
|
Neurotoxicity Syndromes
|
|
Neurotoxicity Syndrome
|
Encephalopathy, Toxic
|
|
|
| C Syndrome |
|
Opitz Trigonocephaly Syndrome
|
Trigonocephaly
|
|
Trigonocephaly Syndrome
|
Trigonocephaly C Syndrome
|
|
Opitz C Trigonocephaly
|
Opitz Trigonocephaly C Syndrome
|
|
Otcs
|
CSYN
|
|
|
| Alacrima, Achalasia, And Mental Retardation Syndrome |
|
AAMR
|
Alacrima, Achalasia, And Intellectual Disability Syndrome
|
|
Alacrima, Achalasia, And Impaired Intellectual Development Syndrome
|
Intellectual Disability
|
|
|
| Sleep Disorder |
|
Sleep Disorders
|
Non-Organic Sleep Disorder
|
|
|
| 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
|
|
|
| Alzheimer'S Disease 1 |
|
Alzheimer Disease Type 1
|
Alzheimer'S Disease 1, Early 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
|
|
|
| Wernicke-Korsakoff Syndrome |
|
Korsakoff Syndrome
|
Transketolase Defect
|
|
Korsakoff'S Syndrome
|
Alcohol-Induced Encephalopathy
|
|
Korsakoff'S Psychosis
|
Korsakov Psychosis
|
|
Korsakov'S Psychosis
|
Alcohol Induced Encephalopathy
|
|
Korsakoff Disease
|
Korsakoff Psychosis
|
|
|
| Cataract |
|
Cataracts
|
Cat - [Cataract]
|
|
Cataract Form
|
Lens Opacity
|
|
Lens Opacities
|
|
|
| Aortic Valve Disease 1 |
|
Aortic Valve Disease
|
Bicuspid Aortic Valve
|
|
Aortic Valve Disorder
|
AOVD1
|
|
Bav
|
Bicuspid Aortic Valve Disease
|
|
Familial Bicuspid Aortic Valve
|
Aortic Valve Calcification
|
|
Aovd
|
Aortic Valve, Bicuspid
|
|
Aortic Valve, Calcification Of
|
Aortic Stenosis, Calcific
|
|
Familial Bav
|
Calcific Aortic Stenosis
|
|
Calcification Of Aortic Valve
|
Abnormality Of The Aortic Valve
|
|
Aortic Valve Disease, Type 1
|
Aortic Valve Disease 2
|
|
Bicommissural Aortic Valve
|
|
|
| Dystonia |
|
Dystonic Disease
|
Dystonic Disorder
|
|
Dystonia Disorders
|
Neuroleptic Dyskinesia
|
|
|
| Macular Degeneration, Age-Related, 4 |
|
Age Related Macular Degeneration 4
|
ARMD4
|
|
Macular Degeneration, Age-Related, Type 4
|
|
|
| Alzheimer Disease 9 |
|
AD9
|
Alzheimer'S Disease 9
|
|
Alzheimer Disease 9, Susceptibility To
|
Alzheimer Disease 9, Late-Onset
|
|
Alzheimer'S Disease 9, Late Onset
|
{Alzheimer Disease 9, Susceptibility To}
|
|
|
| Movement Disease |
|
Movement Disorders
|
Movement Disorder
|
|
|
| Peripheral Vascular Disease |
|
Peripheral Arterial Disease
|
Arterial Occlusive Disease
|
|
Arterial Occlusive Diseases
|
Pad
|
|
Peripheral Vascular Diseases
|
Peripheral Occlusive Disease
|
|
Peripheral Arterial Diseases
|
Helicobacter Infections
|
|
|
| Chromosomal Disease |
|
Chromosomal Disorders
|
Congenital Chromosomal Disease
|
|
|
| Inherited Metabolic Disorder |
|
Inborn Errors Of Metabolism
|
Inborn Metabolic Disorder
|
|
Inborn Metabolism Disorder
|
Metabolic Hereditary Disorder
|
|
Inborn Error Of Metabolism
|
Metabolism, Inborn Errors
|
|
|
| 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
|
|
|
| Schizophrenia |
|
SCZD
|
Schizophrenia With Or Without An Affective Disorder
|
|
Schizophrenia 12
|
Schizophrenia, Susceptibility To
|
|
Schizophrenia-1
|
Dementia Praecox
|
|
Schizophrenia 1
|
|
|
| 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
|
|
|
| Acquired Metabolic Disease |
|
|
| Glucose Metabolism Disease |
|
Glucose Metabolism Disorders
|
Disorder Of Glucose Metabolism
|
|
|
| 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
|
|
|
| Intracranial Berry Aneurysm |
|
Familial Aneurysmal Subarachnoid Hemorrhage
|
Familial Berry Aneurysm
|
|
Familial Intracranial Saccular Aneurysm
|
Saccular Cerebral Aneurysm
|
|
Aneurysm, Intracranial Berry
|
Aneurysmal Subarachnoid Hemorrhage
|
|
Aneurysm, Intracranial Berry, 1
|
|
|
| Thrombocytopenia |
|
Low Platelet Count
|
Low Platelets
|
|
Decreased Platelets
|
Platelet Dysfunction Nos
|
|
|
| Autism |
|
Autistic Disorder
|
Autism Susceptibility 1
|
|
Childhood Autism
|
Autistic Disorder Of Childhood Onset
|
|
Infantile Autism
|
Kanner'S Syndrome
|
|
Autistic
|
|
|
| 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
|
|
|
| Aortic Aneurysm, Familial Thoracic 1 |
|
Thoracic Aortic Aneurysm
|
Annuloaortic Ectasia
|
|
Familial Thoracic Aortic Aneurysm And Aortic Dissection
|
Familial Aortic Dissection
|
|
Familial Taad
|
Familial Thoracic Aortic Aneurysm
|
|
Congenital Aneurysm Of Ascending Aorta
|
Familial Aortic Aneurysm
|
|
Familial Thoracic Aortic Aneurysm And Dissection
|
Aortic Aneurysm, Thoracic
|
|
AAT1
|
Faa1
|
|
Aortic Dissection, Familial
|
Aortic Aneurysm, Familial Thoracic
|
|
Aneurysm, Thoracic Aortic
|
Faa
|
|
Ftaad
|
Taa
|
|
Taad
|
Cystic Medial Necrosis Of Aorta
|
|
Familial Non-Syndromic Thoracic Aortic Aneurysm And Aortic Dissection
|
Aortic Aneurysm Thoracic
|
|
Familial Aortic Aneurysms
|
Aneurysm, Aortic, Thoracic, Familial, Type 1
|
|
Aneurysm Of Thoracic Aorta
|
Intrathoracic Aneurysm
|
|
Thoracic Aorta Aneurysm
|
Thoracic Aortic Aneurysm Without Rupture
|
|
Thoracic Aneurysm
|
Thorax Arterial Aneurysm
|
|
Thoracic Artery Aneurysm
|
Thoracic Arterial Aneurysm
|
|
Thorax Aneurysm
|
Thorax Aortic Aneurysm
|
|
Dissection Of Thoracic Aorta
|
|
|
| Retinitis Pigmentosa |
|
RP
|
Rod-Cone Dystrophy
|
|
Autosomal Recessive Retinitis Pigmentosa
|
Non-Syndromic Retinitis Pigmentosa
|
|
Pericentral Pigmentary Retinopathy
|
Pigmentary Retinopathy
|
|
Tapetoretinal Degeneration
|
Rcd
|
|
Retinitis Pigmentosa Autosomal Recessive
|
ARRP
|
|
Retinitis Pigmentosa, Autosomal Recessive
|
Retinitis Pigmentosa 1
|
|
|
| Niemann-Pick Disease |
|
Sphingomyelin/Cholesterol Lipidosis
|
Niemann-Pick Diseases
|
|
Lipoid Histiocytosis
|
Sphingomyelin Lipidosis
|
|
Sphingomyelinase Deficiency Disease
|
Lipid Histiocytosis
|
|
Neuronal Cholesterol Lipidosis
|
Neuronal Lipidosis
|
|
Npd
|
Sphingomyelinase Deficiency
|
|
Niemann-Pick Disease, Type A
|
|
|
| Specific Developmental Disorder |
|
|
| Systemic Lupus Erythematosus |
|
Lupus Nephritis
|
SLE
|
|
Disseminated Lupus Erythematosus
|
Systemic Lupus Erythematosus, Susceptibility To
|
|
Lupus Erythematosus, Systemic
|
Lupus Nephritis, Susceptibility To
|
|
Libman-Sacks Disease
|
Systemic Lupus Erythematosus Susceptibility To
|
|
Sle - Lupus Erythematosus, Systemic
|
Le Syndrome
|
|
Lupus
|
Lupus Erythematosus Systemic
|
|
Lupus Erythematosus, Systemic, Susceptibility To
|
Lupus Vulgaris
|
|
Lupus Erythematosus, Discoid
|
Lupus Erythematosus
|
|
Systemic Lupus Erythematosus Nos
|
Sle - [Systemic Lupus Erythematosus]
|
|
|
| Psychotic Disorder |
|
Psychotic Disorders
|
Mental Or Behavioural Disorder
|
|
Psychotic
|
Mental Disorders
|
|
|
| Nervous System Disease |
|
Abnormality Of The Nervous System
|
Nervous System Diseases
|
|
Nervous System Disorder
|
|
|
| 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
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Motor Neuron Disease, Bulbar
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Motor Neurone Disease
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Amyotrophic Lateral Sclerosis With Dementia
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Dementia With Amyotrophic Lateral Sclerosis
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Motor Neuron Disease, Amyotrophic Lateral Sclerosis
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Sclerosis, Lateral, Amyotrophic
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Sclerosis, Lateral, Amyotrophic, Type 1
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Amyotrophic Sclerosis
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Als - [Amyotrophic Lateral Sclerosis]
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Wasting Palsy
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Amyotrophic Paralysis
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Amyotrophy Lateral Sclerosis
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Wasting Paralysis
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Spinal Progressive Amyotrophy
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Progressive Atrophic Paralysis
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| Eye Disease |
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Eye Diseases
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Abnormality Of The Eye
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Toxoplasma Oculopathy
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| Peripheral Nervous System Disease |
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Peripheral Neuropathy
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Peripheral Nerve Disease
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Peripheral Nerve Disorders
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Neuropathy, Peripheral
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Peripheral Neuropathy Due To Vitamin Pyridoxine Hyperalimentation
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| Migraine With Or Without Aura 1 |
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Migraine
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Migraine With Or Without Aura, Susceptibility To, 1
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Migraine Disorder
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Migraine Variant
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Migraines
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Migraine Disorders
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Mgr1
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Mgau
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Ma
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Migraine With Or Without Aura
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Classic Migraine
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Common Migraine
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Disorder, Migraine
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Headache Migraine
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Headache Migrainous
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Migraine Headache
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Migraine Syndrome
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Headache Including Migraine
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Migraine, Susceptibility To
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| Attention Deficit-Hyperactivity Disorder |
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Attention Deficit Hyperactivity Disorder
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ADHD
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Attention Deficit Disorder
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Attention Deficit-Hyperactivity Disorder, Susceptibility To
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Attention Deficit Disorder With Hyperactivity
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Hyperkinetic Disorder
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Hyperactivity Of Childhood
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Attention-Deficit/Hyperactivity Disorder
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Add
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Addh
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Attention Deficit
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Attention Deficit Disorder Of Childhood With Hyperactivity
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Attention Deficit Disorder With Hyperactivity Syndrome
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Hyperkinetic Syndrome
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Attention-Deficit Hyperactivity Disorder
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Attention-Deficit/Hyperactivity Disorder, Predominantly Inattentive Type
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Disturbance Of Activity And Attention
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Disorder Of Activity And Attention
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Adhd - [Attention Deficit Hyperactivity Disorder]
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Hyperkinetic Disorders
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Disorder Of Activity And Attention With Hyperkinesia
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Attention Deficit Syndrome With Hyperactivity
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| Dilated Cardiomyopathy |
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Familial Dilated Cardiomyopathy
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Primary Dilated Cardiomyopathy
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Idiopathic Dilated Cardiomyopathy
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Congestive Cardiomyopathy
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Idiopathic Dilation Cardiomyopathy
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Primary Familial Dilated Cardiomyopathy
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Cardiomyopathy, Dilated
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DCM
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Cardiomyopathy, Familial Dilated
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Dilated Cardiomyopathy, Familial
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Hypokinetic Dilated Cardiomyopathy, Familial
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Familial Idiopathic Cardiomyopathy
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Fdc
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Cardiomyopathy, Familial Idiopathic
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Idiopathic Cardiomegaly
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Dilated Congestive Cardiomyopathy
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Chronic Dilated Cardiomyopathy
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Ccm - [Congestive Cardiomyopathy]
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Cocm - [Congestive Cardiomyopathy]
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Dcm - [Dilated Cardiomyopathy]
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Dilated-Hypokinetic Cardiomyopathy
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Congestive Idiopathic Cardiomyopathy
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Primary Idiopathic Dilated Cardiomyopathy
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