| Diseases |
Alias |
|
| 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
|
|
|
| Aapoaii Amyloidosis |
|
Apolipoprotein A-Ii Amyloidosis
|
Familial Amyloid Nephropathy Due To Apolipoprotein A-Ii Variant
|
|
Familial Renal Amyloidosis Due To Apolipoprotein A-Ii Variant
|
Hereditary Amyloid Nephropathy Due To Apolipoprotein A-Ii Variant
|
|
Hereditary Renal Amyloidosis Due To Apolipoprotein A-Ii Variant
|
|
|
| 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
|
|
|
| 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
|
|
|
| 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
|
|
|
| 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
|
|
|
| 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
|
|
|
| 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 |
|
|
| Familial Hyperlipidemia |
|
Familial Hyperlipoproteinemia
|
Hyperlipidaemia
|
|
Hyperlipoproteinemias
|
Hyperlipidemia
|
|
Hyperlipemia
|
Hyperlipidemias
|
|
|
| Carotid Artery Disease |
|
Carotid Artery Diseases
|
Disorder Of Carotid Artery
|
|
|
| Amyloidosis |
|
Amyloid Disease
|
Amyloid
|
|
Amyloid Degeneration
|
Amyloidosis Nos
|
|
Amyloid Deposition
|
Amyloid Infiltration
|
|
Idiopathic Amyloidosis
|
Hyaloid Degeneration
|
|
Lardaceous Degeneration
|
|
|
| Hypertriglyceridemia 1 |
|
Hypertriglyceridemia
|
Hypertriglyceridemia, Familial
|
|
Hypertriglyceridemia, Susceptibility To
|
HYTG1
|
|
FHTR
|
Hypertriglyceridemias Familial
|
|
|
| Apolipoprotein A-Iv Associated Amyloidosis |
|
Aapoaiv Amyloidosis
|
Renal Aapoaiv Amyloidosis
|
|
Apolipoprotein A-Iv Amyloidosis
|
|
|
| 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
|
|
|
| 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
|
|
|
| Thrombophilia Due To Hrg Deficiency |
|
Hereditary Thrombophilia Due To Congenital Histidine-Rich Glycoprotein Deficiency
|
Hereditary Thrombophilia Due To Congenital Hrg Deficiency
|
|
Thph11
|
|
|
| Immunoglobulin Heavy-And-Light Chain |
|
Ah/Al Amyloidosis
|
Ig Heavy-And-Light-Chain Amyloidosis
|
|
|
| Polyneuropathy |
|
|
| 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
|
|
|
| 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
|
|
|
| Atherosclerosis Susceptibility |
|
Atherosclerosis
|
Atherosclerosis, Susceptibility To
|
|
ATHS
|
Atherogenic Lipoprotein Phenotype
|
|
Alp
|
Arteriosclerosis
|
|
|
| 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
|
|
|
| Dialysis-Related Amyloidosis |
|
Abeta2m Amyloidosis
|
Amyloidosis Beta2m
|
|
Beta2-Microglobulinic Amyloidosis
|
Variant Abeta2m Amyloidosis
|
|
Autosomal Dominant Beta2-Microglobulinic Amyloidosis
|
Aβ2m Amyloidosis
|
|
Dialysis-Related Beta2-Microglobulin Amyloidosis
|
Amyloidosis Dialysis-Related
|
|
Beta-2-Microglobulin Amyloidosis
|
Dra
|
|
Hemodialysis-Associated Amyloidosis
|
|
|
| Type 1 Diabetes Mellitus 6 |
|
Diabetes Mellitus, Insulin-Dependent, 6
|
Iddm6
|
|
Insulin-Dependent Diabetes Mellitus 6
|
T1D6
|
|
Insulin-Dependent Diabetes Mellitus-6
|
|
|
| Immunoglobulin Heavy Chain Amyloidosis |
|
Ah Amyloidosis
|
Heavy Chain Amyloidosis
|
|
Amyloidosis Derived From Immunoglobulin Heavy Chain
|
Ig Heavy-Chain-Associated Amyloidosis
|
|
|
| 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
|
|
|
| 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
|
|
|
| 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
|
|
|
| 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
|
|
|
| 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
|
|
|
| Vascular Disease |
|
Vascular Diseases
|
Aneurysm
|
|
Spinal Cord Ischemia
|
Vascular Anomaly
|
|
Spinal Cord Vascular Diseases
|
Vascular Tissue Disease
|
|
|
| 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
|
|
|
| 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
|
|
|
| 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
|
|
|
| Diabetes Mellitus |
|
|
| Cardiovascular System Disease |
|
Abnormality Of The Cardiovascular System
|
Cardiovascular Disease
|
|
Disease Of Subdivision Of Hemolymphoid System
|
Disorder Of Cardiovascular System
|
|
Cardiovascular Diseases
|
|
|
| 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
|
|
|
