| Diseases |
Alias |
|
| Hypoalphalipoproteinemia, Primary, 2 |
|
Apolipoprotein A-I Deficiency
|
Hypoalphalipoproteinemia, Primary, 2, Autosomal Recessive
|
|
Primary Hypoalphalipoproteinemia 2
|
High Density Lipoprotein Deficiency
|
|
Apoa-I Deficiency
|
Familial Apoa-I Deficiency
|
|
Familial Hypoalphalipoproteinemia
|
FHA2
|
|
Apolipoprotein A-I
|
|
|
| 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
|
|
|
| Hypoalphalipoproteinemia, Primary, 2, Intermediate |
|
Hypoalphalipoproteinemia, Primary, 2, Autosomal Dominant
|
FHA2I
|
|
|
| Aapoai Amyloidosis |
|
Apolipoprotein A-I Amyloidosis
|
Familial Amyloid Nephropathy Due To Apolipoprotein A-I Variant
|
|
Familial Renal Amyloidosis Due To Apolipoprotein A-I Variant
|
Hereditary Amyloid Nephropathy Due To Apolipoprotein A-I Variant
|
|
Hereditary Renal Amyloidosis Due To Apolipoprotein A-I Variant
|
|
|
| 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
|
|
|
| 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
|
|
|
| Spastic Paraplegia 50, Autosomal Recessive |
|
Hereditary Spastic Paraplegia 50
|
SPG50
|
|
Ap-4 Deficiency Syndrome
|
Ap-4-Associated Hereditary Spastic Paraplegia
|
|
Adaptor Protein Complex 4 Deficiency
|
Cerebral Palsy, Spastic Quadriplegic, 3, Formerly
|
|
Cpsq3, Formerly
|
Autosomal Recessive Spastic Paraplegia 50
|
|
Cpsq3
|
Spastic Quadriplegic Cerebral Palsy 3
|
|
Ap-4 Deficiency
|
Ap-4-Associated Hsp
|
|
Paraplegia, Spastic, Autosomal Recessive, Type 50
|
Spastic Paraplegia-50, Autosomal Recessive
|
|
|
| Hypoalphalipoproteinemia |
|
|
| Familial Hyperlipidemia |
|
Familial Hyperlipoproteinemia
|
Hyperlipidaemia
|
|
Hyperlipoproteinemias
|
Hyperlipidemia
|
|
Hyperlipemia
|
Hyperlipidemias
|
|
|
| Coronary Stenosis |
|
|
| Amyloidosis |
|
Amyloid Disease
|
Amyloid
|
|
Amyloid Degeneration
|
Amyloidosis Nos
|
|
Amyloid Deposition
|
Amyloid Infiltration
|
|
Idiopathic Amyloidosis
|
Hyaloid Degeneration
|
|
Lardaceous Degeneration
|
|
|
| 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
|
|
|
| Arteriosclerosis |
|
Arteriosclerotic Vascular Disease
|
|
|
| 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
|
|
|
| Hereditary Amyloidosis |
|
Amyloidosis Hereditary
|
Familial Amyloidosis
|
|
Amyloidosis Familial
|
Amyloidosis, Hereditary
|
|
Amyloidosis, Familial
|
Genetic Amyloidosis
|
|
Heredofamilial Amyloidosis
|
|
|
| Arcus Corneae |
|
Arcus Senilis
|
Corneal Arcus
|
|
Arcus Of Cornea
|
|
|
| Cerebral Atherosclerosis |
|
Intracranial Arteriosclerosis
|
|
|
| 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
|
|
|
| Fish-Eye Disease |
|
FED
|
Dyslipoproteinemic Corneal Dystrophy
|
|
Alpha-Lcat Deficiency
|
Lcata Deficiency
|
|
Partial Lcat Deficiency
|
Alpha-Lecithin:Cholesterol Acyltransferase Deficiency
|
|
Alpha-Lecithin Cholesterol Acyltransferase Deficiency
|
Disease, Fish-Eye
|
|
Lecithin Acyltransferase Deficiency
|
|
|
| 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
|
|
|
| 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
|
|
|
| Polyneuropathy |
|
|
| 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
|
|
|
| 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
|
|
|
| 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
|
|
|
| Atherosclerosis Susceptibility |
|
Atherosclerosis
|
Atherosclerosis, Susceptibility To
|
|
ATHS
|
Atherogenic Lipoprotein Phenotype
|
|
Alp
|
Arteriosclerosis
|
|
|
| Hypertriglyceridemia 1 |
|
Hypertriglyceridemia
|
Hypertriglyceridemia, Familial
|
|
Hypertriglyceridemia, Susceptibility To
|
HYTG1
|
|
FHTR
|
Hypertriglyceridemias Familial
|
|
|
| Cardiovascular System Disease |
|
Abnormality Of The Cardiovascular System
|
Cardiovascular Disease
|
|
Disease Of Subdivision Of Hemolymphoid System
|
Disorder Of Cardiovascular System
|
|
Cardiovascular Diseases
|
|
|
| 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
|
|
|
| Vascular Disease |
|
Vascular Diseases
|
Aneurysm
|
|
Spinal Cord Ischemia
|
Vascular Anomaly
|
|
Spinal Cord Vascular Diseases
|
Vascular Tissue Disease
|
|
|
| Nephrotic Syndrome |
|
Finnish Congenital Nephrotic Syndrome
|
Ns - [Nephrotic Syndrome]
|
|
Nephrosis Syndrome
|
Nephrosis Nos
|
|
Glomerular Lesion Nephrosis
|
|
|
| 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
|
|
|
| Angina Pectoris |
|
Prinzmetal'S Variant Angina
|
Angina
|
|
Prinzmetal Angina
|
Variant Angina
|
|
Angina Inversa
|
Prinzmetal'S Angina
|
|
Coronary Artery Vasospasm
|
Angina Pectoris, Variant
|
|
Variant Angina Pectoris
|
Vasospastic Angina
|
|
Angor Pectoris
|
Anginal Syndrome
|
|
Ischaemic Chest Pain
|
Angina Pectoris Syndrome
|
|
Angina Syndrome
|
Cardiac Angina Syndrome
|
|
Ap - [Angina Pectoris]
|
Angina Nos
|
|
Ap - [Angina Pectoris] Syndrome
|
Ischaemic Heart Disease With Angina
|
|
Heart Angina
|
Chest Angina
|
|
Angina Attack
|
Anginal Cardiopathy
|
|
Coronary Pain Nos
|
|
|
| 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
|
|
|
| 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
|
|
|
| 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
|
|
|
| Fetal Macrosomia |
|
|
| 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
|
|
|
| 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
|
|
|
| Acute Myocardial Infarction |
|
Cardiac Attack
|
Heart Attack
|
|
|
| Hepatoblastoma |
|
|
| 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
|
|
|
| Amyloid Neuropathy |
|
Amyloid Neuropathies
|
Neuropathy Amyloid
|
|
|
| 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
|
|
|
| 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
|
|
|
| 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
|
|
|
| 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
|
|
|
| Sleeping Sickness |
|
African Trypanosomiasis
|
African Sleeping Sickness
|
|
Trypanosomiasis, Human East-African
|
Trypanosomiasis, East African
|
|
Trypanosomiasis African
|
Trypanosomiasis, African
|
|
Human African Trypanosomiasis
|
|
|
| Pyloric Stenosis |
|
|
| 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
|
|
|
| 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
|
|
|
| Diabetes Mellitus |
|
|
| 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
|
|
|
| Varicose Veins |
|
Varices
|
Varix
|
|
Venous Ectasia
|
Venous Varices
|
|
Varicosity
|
|
|
| Glucose Intolerance |
|
Glucose: Intolerance
|
Glucose: Malabsorption
|
|
Malabsorption Of Glucose
|
Impaired Glucose Tolerance
|
|
|
| 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
|
|
|
| Cerebrovascular Disease |
|
Cerebrovascular Disorder
|
Cerebrovascular Accident
|
|
Cerebrovascular Disorders
|
Cva
|
|
Stroke
|
|
|
| Apolipoprotein A-Iv Associated Amyloidosis |
|
Aapoaiv Amyloidosis
|
Renal Aapoaiv Amyloidosis
|
|
Apolipoprotein A-Iv Amyloidosis
|
|
|
| Nonobstructive Coronary Artery Disease |
|
Non-Cad
|
Non-Obstructive Coronary Artery Disease
|
|
|
| Peripheral Vascular Disease |
|
Peripheral Arterial Disease
|
Arterial Occlusive Disease
|
|
Arterial Occlusive Diseases
|
Pad
|
|
Peripheral Vascular Diseases
|
Peripheral Occlusive Disease
|
|
Peripheral Arterial Diseases
|
Helicobacter Infections
|
|
|
| Budd-Chiari Syndrome |
|
Hepatic Vein Thrombosis
|
Chiari Syndrome
|
|
BDCHS
|
Membranous Obstruction Of The Inferior Vena Cava
|
|
Budd-Chiari Syndrome, Somatic
|
Movc
|
|
Budd-Chiari Syndrome, Susceptibility To, Somatic
|
Budd-Chiari Syndrome, Susceptibility To
|
|
Membranous Obstruction Of Inferior Vena Cava
|
Hepatic Vein Block
|
|
Obstruction Of Hepatic Veins
|
Hepatic Vein Obstruction
|
|
Hepatic Venous Block
|
|
|
| Prediabetes Syndrome |
|
Prediabetes
|
Impaired Glucose Tolerance
|
|
Prediabetic State
|
IGT
|
|
Igt - [Impaired Glucose Tolerance]
|
Impaired Glucose Tolerance With Unspecified Complication
|
|
Impaired Glucose Tolerance Without Complication
|
Abnormal Glucose Tolerance
|
|
|
| Psoriatic Arthritis |
|
Psoriatic Arthritis, Susceptibility To
|
Psoriatic Arthropathy
|
|
Arthropathic Psoriasis
|
Arthritis, Psoriatic
|
|
Arthritis Psoriatica
|
PSORAS
|
|
Arthritic Psoriasis
|
Psoriasis Arthropathica
|
|
Arthritis Psoriatic
|
Arthritis, Psoriatic, Susceptibility To
|
|
|
| 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
|
|
|
| Tobacco Addiction |
|
Nicotine Dependence
|
Tobacco Addiction, Susceptibility To
|
|
Nicotine Addiction
|
Tobacco Use Disorder
|
|
Smoking Habit
|
Nicotine Dependence, Protection Against
|
|
Nicotine Addiction, Protection From
|
Cigarette Habituation
|
|
Cigarette Habituation, Susceptibility To
|
Smoking Habit, Susceptibility To
|
|
Nicotine Dependence, Susceptibility To
|
Nicotine Addiction, Susceptibility To
|
|
Addiction, Tobacco, Susceptibility To
|
Compulsive Tobacco User Syndrome
|
|
Tobacco Dependence
|
Tobacco Dependence Syndrome
|
|
Cigarette Addiction
|
Cigarette Dependence
|
|
Smoking Addiction
|
Smokers Syndrome
|
|
|
| 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
|
|
|
| Myelitis |
|
Spinal Cord Inflammation Nos
|
Radiculomyelitis Nos
|
|
Myeloradiculitis
|
|
|
| Acquired Immunodeficiency Syndrome |
|
Acquired Immune Deficiency Syndrome
|
AIDS
|
|
Acquired Immune Deficiency
|
Acquired Immunodeficiency
|
|
Acquired Immunodeficiency Due To Protein Loss
|
|
|
| Childhood Testicular Germ Cell Tumor |
|
Paediatric Testicular Germ Cell Neoplasm
|
Paediatric Testicular Germ Cell Tumour
|
|
Pediatric Testicular Germ Cell Neoplasm
|
Pediatric Testicular Germ Cell Tumor
|
|
Testicular Germ Cell Tumor, Pediatric
|
|
|
| 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
|
|
|
| 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
|
|
|
| Hypothyroidism |
|
Thyroid Diseases
|
Thyroid Disease
|
|
Thyroid Deficiency
|
Thyroid Insufficiency
|
|
Dysfunction Thyroid
|
Thyroid Dysfunction
|
|
|
| Silent Myocardial Infarction |
|
|
| 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
|
|
|
| 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
|
|
|
| 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
|
|
|
| Hypobetalipoproteinemia, Familial, 2 |
|
Familial Hypobetalipoproteinemia 2
|
FHBL2
|
|
Hypolipidemia, Familial, Combined
|
Combined Familial Hypolipidemia
|
|
Combined Hypobetalipoproteinemia Familial
|
Hypobetalipoproteinemia, Familial, Type 2
|
|
|
| Pulmonary Coin Lesion |
|
Coin Lesion Of Lung
|
Solitary Pulmonary Nodule
|
|
Coin Lesion Lung
|
|
|
| Intermediate Coronary Syndrome |
|
Unstable Angina
|
Angina At Rest
|
|
Anginal Chest Pain At Rest
|
Impending Infarction
|
|
Preinfarction Angina
|
Worsening Angina
|
|
Angina, Unstable
|
Myocardial Preinfarction Syndrome
|
|
Angina Unstable
|
Crescendo Angina
|
|
Angina Decubitus
|
Acute Coronary Insufficiency
|
|
Unstable Angina Pectoris
|
Preinfarctional Angina Pectoris
|
|
Worsening Effort Angina
|
Preinfarction Syndrome
|
|
Unstable Angina Pectoris Syndrome
|
Unstable Anginal Attack
|
|
Unstable Cardiac Angina
|
Unstable Chest Angina
|
|
Unstable Heart Angina
|
De Novo Effort Angina Pectoris
|
|
Crescendo Angina Pectoris
|
Ua - [Unstable Angina]
|
|
|
| Alagille Syndrome 1 |
|
Alagille Syndrome
|
Arteriohepatic Dysplasia
|
|
Alagille-Watson Syndrome
|
Cholestasis With Peripheral Pulmonary Stenosis
|
|
Hepatic Ductular Hypoplasia
|
Alagille Syndrome Due To A Jag1 Point Mutation
|
|
ALGS1
|
Algs
|
|
Aws
|
Syndromic Bile Duct Paucity
|
|
Cardiovertebral Syndrome
|
Hepatofacioneurocardiovertebral Syndrome
|
|
Paucity Of Interlobular Bile Ducts
|
Watson-Miller Syndrome
|
|
Alagille Syndrome Due To 20p12 Microdeletion
|
Ahd
|
|
Hepatic Ductular Hypoplasia, Syndromatic
|
Watson Alagille Syndrome
|
|
Alagille'S Syndrome
|
Alagille Syndrome Due To Del(20)(P12)
|
|
Alagille Syndrome Due To Monosomy 20p12
|
Alagille-Watson Syndrome Due To Monosomy 20p12
|
|
Arteriohepatic Dysplasia Due To Monosomy 20p12
|
Syndromic Bile Duct Paucity Due To Monosomy 20p12
|
|
Alagille-Watson Syndrome Due To A Jag1 Point Mutation
|
Arteriohepatic Dysplasia Due To A Jag1 Point Mutation
|
|
Syndromic Bile Duct Paucity Due To A Jag1 Point Mutation
|
Alagille Syndrome, Type 1
|
|
|
| Corneal Degeneration |
|
Degenerative Corneal Opacity
|
|
|
| Carotid Artery Disease |
|
Carotid Artery Diseases
|
Disorder Of Carotid Artery
|
|
|
| Prader-Willi Syndrome |
|
Prader-Labhart-Willi Syndrome
|
PWS
|
|
Willi-Prader Syndrome
|
Prader-Willi Syndrome Due To Translocation
|
|
Prader-Willi Syndrome Due To Imprinting Mutation
|
Prader-Willi Syndrome Due To Maternal Uniparental Disomy Of Chromosome 15
|
|
Prader Willi Syndrome
|
Upd(15)Mat
|
|
|
| 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
|
|
|
| Deafness, Autosomal Recessive 74 |
|
DFNB74
|
Autosomal Recessive Nonsyndromic Deafness 74
|
|
Autosomal Recessive Deafness 74
|
Deafness, Autosomal Recessive, 74
|
|
Deafness, Autosomal Recessive, Type 74
|
|
|
| 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
|
|
|
| Arteries, Anomalies Of |
|
Artery Disease
|
Arteriopathic Disease
|
|
|
| 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
|
|
|
| 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 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
|
|
|
| Asymmetric Motor Neuropathy |
|
|
| Ichthyosis, Congenital, Autosomal Recessive 4a |
|
Ichthyosis Congenita Iib
|
Icr2b
|
|
Autosomal Recessive Congenital Ichthyosis 4a
|
ARCI4A
|
|
Lamellar Ichthyosis 2
|
Li2
|
|
Ichthyosis, Lamellar, 2, Formerly
|
Li2, Formerly
|
|
Ichthyosis Lamellar 2
|
Lamellar Ichthyosis, Type 2
|
|
Ichthyosis, Lamellar 2
|
Ichthyosis, Congenital, Autosomal Recessive, Type 4a
|
|
|
| Inflammatory Bowel Disease |
|
Inflammatory Bowel Diseases
|
Bowel Disease, Inflammatory
|
|
|
| Cardiomyopathy, Dilated, 1m |
|
Dilated Cardiomyopathy 1m
|
CMD1M
|
|
Cardiomyopathy, Dilated 1m
|
Cardiomyopathy, Dilated, Type 1m
|
|
|
| Nervous System Disease |
|
Abnormality Of The Nervous System
|
Nervous System Diseases
|
|
Nervous System Disorder
|
|
|
