| Diseases |
Alias |
|
| 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
|
|
|
| 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
|
|
|
| Hypoalphalipoproteinemia |
|
|
| 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
|
|
|
| Eye Disease |
|
Eye Diseases
|
Abnormality Of The Eye
|
|
Toxoplasma Oculopathy
|
|
|
| Familial Hyperlipidemia |
|
Familial Hyperlipoproteinemia
|
Hyperlipidaemia
|
|
Hyperlipoproteinemias
|
Hyperlipidemia
|
|
Hyperlipemia
|
Hyperlipidemias
|
|
|
| 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
|
|
|
| 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
|
|
|
| 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
|
|
|
| Arcus Corneae |
|
Arcus Senilis
|
Corneal Arcus
|
|
Arcus Of Cornea
|
|
|
| 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
|
|
|
| Algoneurodystrophy |
|
Reflex Sympathetic Dystrophy
|
Algoneurodystrophy, Site Unspecified
|
|
|
| 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
|
|
|
| Cholesterol Ester Storage Disease |
|
|
| 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
|
|
|
| Kwashiorkor |
|
Kwashiokor
|
Nutritional Edema With Dyspigmentation Of Skin And Hair
|
|
Nutritional Oedema With Dyspigmentation Of Skin And/Or Hair
|
|
|
| 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
|
|
|
| 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
|
|
|
| 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
|
|
|
| Peripheral Vascular Disease |
|
Peripheral Arterial Disease
|
Arterial Occlusive Disease
|
|
Arterial Occlusive Diseases
|
Pad
|
|
Peripheral Vascular Diseases
|
Peripheral Occlusive Disease
|
|
Peripheral Arterial Diseases
|
Helicobacter Infections
|
|
|
| Uremia |
|
|
| Atherosclerosis Susceptibility |
|
Atherosclerosis
|
Atherosclerosis, Susceptibility To
|
|
ATHS
|
Atherogenic Lipoprotein Phenotype
|
|
Alp
|
Arteriosclerosis
|
|
|
| Mucolipidosis |
|
|
| Cystinosis |
|
Cystine Storage Disease
|
Cystine Diathesis
|
|
Cystine Disease
|
Cystinoses
|
|
Protein Defect Of Cystin Transport
|
Cystin Transport, Protein Defect Of
|
|
Nephropathic Cystinosis
|
Protein Defect Of Cystine Transport
|
|
|
| Corneal Disease |
|
Corneal Diseases
|
Corneal Disorders
|
|
|
| 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
|
|
|
| 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
|
|
|
| Nephrosclerosis |
|
|
| Hemolytic Anemia |
|
Anemia, Hemolytic
|
Anemia Hemolytic
|
|
Anaemia Due To Other Disorders Of Glutathione Metabolism
|
Chronic Non Spherocytic Anaemia
|
|
G6pd - [Glucose-6-Phosphate Dehydrogenase Deficiency] Anaemia
|
Anaemia Due To Glucose-6-Phosphate Dehydrogenase Deficiency
|
|
Glucose-6-Phosphate Dehydrogenase Deficiency With Anaemia
|
Glucose-6-Phosphate Dehydrogenase Deficiency Anaemia
|
|
Favism Anaemia
|
Haemolytic Anaemia Due Tog6pd Deficiency
|
|
Favism
|
Pentose Phosphate Pathway Disorder Anaemia
|
|
Anaemia Due To Pentose Phosphate Pathway Defect
|
|
|
| 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
|
|
|
| Fetal Macrosomia |
|
|
| Nephrotic Syndrome |
|
Finnish Congenital Nephrotic Syndrome
|
Ns - [Nephrotic Syndrome]
|
|
Nephrosis Syndrome
|
Nephrosis Nos
|
|
Glomerular Lesion Nephrosis
|
|
|
| Monocarboxylate Transporter 1 Deficiency |
|
Ketoacidosis Due To Monocarboxylate Transporter-1 Deficiency
|
MCT1D
|
|
Ketosis
|
|
|
| Sea-Blue Histiocyte Disease |
|
Sea-Blue Histiocytosis
|
Sea-Blue Histiocyte Syndrome
|
|
Histiocytosis, Sea-Blue
|
Inherited Lipemic Splenomegaly
|
|
SBHD
|
|
|
| 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
|
|
|
| Obstructive Jaundice |
|
Jaundice, Obstructive
|
Cholestatic Jaundice
|
|
Cholestatic Jaundice Syndrome
|
Obstructive Hyperbilirubinemia
|
|
Jaundice Obstructive
|
Jaundice Cholestatic
|
|
|
| Lysosomal And Lipase Deficiency |
|
|
| Alcoholic Liver Cirrhosis |
|
Alcoholic Cirrhosis
|
Portal Cirrhosis
|
|
Alcoholic Cirrhosis Of Liver
|
Liver Cirrhosis, Alcoholic
|
|
Laennec'S Cirrhosis
|
Laennec'S Cirrhosis, Alcoholic
|
|
Alcohol Cirrhosis
|
Alcoholic Laennec Cirrhosis
|
|
Alcoholic Cirrhosis Nos
|
Etoh Cirrhosis
|
|
Alcohol Hepatic Cirrhosis
|
Alcohol Liver Cirrhosis
|
|
Laennec Cirrhosis
|
|
|
| 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
|
|
|
| Lysosomal Acid Lipase Deficiency |
|
Wolman Disease
|
Cholesteryl Ester Storage Disease
|
|
Lal Deficiency
|
Lipa Deficiency
|
|
Cholesterol Ester Storage Disease
|
CESD
|
|
Cholesterol Ester Hydrolase Deficiency
|
Acid Lipase Deficiency
|
|
Acid Esterase Deficiency
|
Familial Xanthomatosis
|
|
Wolman Xanthomatosis
|
Wolman'S Disease
|
|
Wolman'S Or Triglyceride Storage Type Iii Disease
|
Xanthomatosis, Familial
|
|
Liposomal Acid Lipase Deficiency, Wolman Type
|
Familial Visceral Xanthomatosis
|
|
Primary Familial Xanthomatosis
|
Primary Familial Xanthomatosis With Adrenal Calcification
|
|
Acid Lipase Disease
|
WOD
|
|
Acid Cholesteryl Ester Hydrolase Deficiency, Type 2
|
|
|
| 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
|
|
|
| Cardiovascular System Disease |
|
Abnormality Of The Cardiovascular System
|
Cardiovascular Disease
|
|
Disease Of Subdivision Of Hemolymphoid System
|
Disorder Of Cardiovascular System
|
|
Cardiovascular Diseases
|
|
|
| Corneal Dystrophy, Meesmann, 1 |
|
Meesmann Corneal Dystrophy
|
Mecd
|
|
Corneal Dystrophy, Meesmann Epithelial
|
Juvenile Hereditary Epithelial Dystrophy
|
|
Corneal Dystrophy, Juvenile Epithelial Of Meesmann
|
MECD1
|
|
Meesmann Corneal Dystrophy 1
|
Meesmann Corneal Epithelial Dystrophy
|
|
Meesmann Epithelial Corneal Dystrophy
|
Corneal Dystrophy, Juvenile Epithelial, Of Meesmann
|
|
Stocker-Holt Dystrophy
|
Meesman Dystrophy
|
|
Meesman'S Corneal Dystrophy
|
Juvenile Hereditary Epithelial Dystrophy Of Meesmann
|
|
Corneal Dystrophy, Meesmann 1
|
Juvenile Epithelial Corneal Dystrophy Of Meesmann
|
|
Mcd
|
Dystrophy, Corneal, Meesmann
|
|
|
| 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
|
|
|
| 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
|
|
|
| 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
|
|
|
| Diabetes Mellitus |
|
|
| Deficiency Anemia |
|
Anemia
|
Deficiency Anemias
|
|
Anaemia
|
|
|
| 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
|
|
|
| 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
|
|
|
