| Diseases |
Alias |
|
| Adiponectin, Serum Level Of, Quantitative Trait Locus 1 |
|
Adiponectin Deficiency
|
ADIPQTL1
|
|
ADPND
|
|
|
| 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
|
|
|
| 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
|
|
|
| Glucose Intolerance |
|
Glucose: Intolerance
|
Glucose: Malabsorption
|
|
Malabsorption Of Glucose
|
Impaired Glucose Tolerance
|
|
|
| Gestational Diabetes |
|
Gestational Diabetes Mellitus
|
GDM
|
|
Diabetes Mellitus Arising In Pregnancy
|
Maternal Gestational Diabetes Mellitus
|
|
Diabetes Mellitus, Gestational
|
Diabetes Mellitus, Pregnancy Related
|
|
Diabetes, Pregnancy-Induced
|
Diabetes Gestational
|
|
Diabetes, Gestational
|
Diabetes Of Pregnancy
|
|
Gdm - [Gestational Diabetes Mellitus]
|
Gestational Diabetes Mellitus Nos
|
|
Gestational Diabetes Complicating Pregnancy, Childbirth, Or The Puerperium
|
|
|
| Liver Disease |
|
Liver Failure
|
Liver Diseases
|
|
Abnormality Of The Liver
|
Liver Dysfunction
|
|
Disorder Of Liver
|
Hepatic Disorder
|
|
Hepatic Disease
|
Disease Of Bilirubin Metabolism
|
|
Disorder Of Bilirubin Metabolism
|
Liver Decompensation
|
|
Liver Function Failure
|
Hepatic Failure Nos
|
|
Liver Failure Nos
|
End Stage Liver Disease
|
|
Decompensated Liver Failure
|
Decompensation Of Liver Function
|
|
Hepatic Decompensation
|
Hepatic Insufficiency
|
|
Liver Cell Necrosis With Hepatic Failure
|
Liver Insufficiency
|
|
Decompensated Liver Disease
|
End Stage Liver Failure
|
|
Liver Necrosis With Hepatic Failure
|
|
|
| Acquired Generalized Lipodystrophy |
|
Lawrence Syndrome
|
Acquired Lipoatrophic Diabetes
|
|
Lawrence-Seip Syndrome
|
Familial Generalized Lipodystrophy
|
|
|
| Hyperglycemia |
|
|
| Obesity-Hypoventilation Syndrome |
|
Obesity Hypoventilation Syndrome
|
Pickwickian Syndrome
|
|
Cardiopulmonary Obesity Syndrome
|
Extreme Obesity With Alveolar Hypoventilation With Body-Mass-Index Unspecified
|
|
Alveolar Hypoventilation Syndrome
|
Alveolus Hypoventilation Syndrome
|
|
Ohs - [Obesity Hypoventilation Syndrome]
|
|
|
| Arteriolosclerosis |
|
|
| Leptin Deficiency Or Dysfunction |
|
Morbid Obesity
|
Obesity Due To Congenital Leptin Deficiency
|
|
LEPD
|
Congenital Leptin Deficiency
|
|
Obesity, Morbid
|
Obesity, Morbid, Due To Leptin Deficiency
|
|
Severe Obesity
|
Obesity, Morbid, Nonsyndromic 1
|
|
Leptin Deficiency
|
Obesity, Severe, Due To Leptin Deficiency
|
|
Leptin
|
Morbid Obesity Due To Leptin Deficiency
|
|
Obesity Morbid
|
Leptin Dysfunction
|
|
|
| Diabetes Mellitus |
|
|
| Acanthosis Nigricans |
|
|
| Anorexia Nervosa |
|
Anorexia Nervosa, Susceptibility To
|
ANON
|
|
Anorexia Nervosa, Susceptibility To, 1
|
An
|
|
Anorexia Nervosa 1
|
An - [Anorexia Nervosa]
|
|
|
| Arteriosclerosis Obliterans |
|
|
| 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
|
|
|
| Arteriosclerosis |
|
Arteriosclerotic Vascular Disease
|
|
|
| Abdominal Obesity-Metabolic Syndrome 1 |
|
Metabolic Syndrome X
|
Metabolic Syndrome
|
|
AOMS1
|
Dysmetabolic Syndrome X
|
|
Metabolic Disease
|
Abdominal Obesity Metabolic Syndrome
|
|
|
| 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
|
|
|
| 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
|
|
|
| Proteasome-Associated Autoinflammatory Syndrome 1 |
|
Jmp Syndrome
|
Nakajo-Nishimura Syndrome
|
|
Nkjo
|
Autoinflammation, Lipodystrophy, And Dermatosis Syndrome
|
|
Proteasome-Associated Autoinflammatory Syndrome 1 And Digenic Forms
|
Nakajo Syndrome
|
|
PRAAS1
|
Chronic Atypical Neutrophilic Dermatosis With Lipodystrophy And Elevated Temperature Syndrome
|
|
Candle
|
Joint Contractures, Muscular Atrophy, Microcytic Anemia, And Panniculitis-Induced Lipodystrophy
|
|
Aldd
|
Inflammation
|
|
Joint Contractures - Muscle Atrophy - Microcytic Anemia - Panniculitis-Induced Lipodystrophy
|
Nakajo Nishimura Syndrome
|
|
Amyotrophy Fat Tissue Anomaly
|
Japanese Autoinflammatory Syndrome With Lipodystrophy
|
|
Jasl
|
Joint Contractures Muscular Atrophy Microcytic Anemia And Panniculitis-Induced Lipodystrophy
|
|
Nns
|
Nodular Erythema With Digital Changes
|
|
Secondary Hypertrophic Osteoperiostosis With Pernio
|
|
|
| Sleep Apnea |
|
|
| Hyperandrogenism |
|
Hyperandrogenization Syndrome
|
|
|
| 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
|
|
|
| Polycystic Ovary Syndrome |
|
Polycystic Ovarian Syndrome
|
Pcos
|
|
Polycystic Ovarian Disease
|
Polycystic Ovaries
|
|
Stein-Leventhal Syndrome
|
Multicystic Ovaries
|
|
Polycystic Ovary
|
Sclerocystic Ovaries
|
|
Sclerocystic Ovary Syndrome
|
Stein-Leventhal Synd.
|
|
Cystic Disease Of Ovaries
|
Cystic Disease Of Ovary
|
|
Pco
|
Pcod
|
|
Sclerocystic Ovarian Degeneration
|
Polycystic Ovary Syndrome, Susceptibility To
|
|
Pcos - [Polycystic Ovary Syndrome]
|
Polycystic Ovary Nos
|
|
Pco - [Polycystic Ovary]
|
|
|
| Cardiovascular System Disease |
|
Abnormality Of The Cardiovascular System
|
Cardiovascular Disease
|
|
Disease Of Subdivision Of Hemolymphoid System
|
Disorder Of Cardiovascular System
|
|
Cardiovascular Diseases
|
|
|
| Severe Pre-Eclampsia |
|
Severe Preeclampsia
|
Antepartum Severe Pre-Eclampsia
|
|
Postpartum Severe Pre-Eclampsia
|
Severe Pre-Eclampsia, With Delivery
|
|
Severe Toxemia
|
Severe Pre-Eclampsia, Antepartum Condition Or Complication
|
|
Severe Pre-Eclampsia, Postpartum Condition Or Complication
|
Severe Puerperal Pre-Eclampsia
|
|
Severe Pre-Eclamptic Toxaemia
|
Severe Pet - [Pre-Eclamptic Toxaemia]
|
|
|
| Vascular Disease |
|
Vascular Diseases
|
Aneurysm
|
|
Spinal Cord Ischemia
|
Vascular Anomaly
|
|
Spinal Cord Vascular Diseases
|
Vascular Tissue Disease
|
|
|
| Laron Syndrome |
|
Growth Hormone Insensitivity Syndrome
|
Growth Hormone Receptor Deficiency
|
|
Laron Dwarfism
|
Pituitary Dwarfism Ii
|
|
Laron-Type Isolated Somatotropin Defect
|
Primary Growth Hormone Resistance
|
|
Laron-Type Dwarfism
|
Laron Type Pituitary Dwarfism I
|
|
Primary Growth Hormone Insensitivity
|
Primary Gh Resistance
|
|
Gh-R Deficiency
|
Growth Hormone Receptor Defect
|
|
Laron-Type Pituitary Dwarfism
|
Laron-Type Short Stature
|
|
Severe Gh Insensitivity
|
Ghis
|
|
Short Stature Due To A Defect In Growth Hormone Receptor Or Post-Receptor Pathway
|
Complete Growth Hormone Insensitivity
|
|
Gh Receptor Deficiency
|
Primary Gh Insensitivity
|
|
Short Stature Due To Growth Hormone Resistance
|
LARS
|
|
|
| Atherosclerosis Susceptibility |
|
Atherosclerosis
|
Atherosclerosis, Susceptibility To
|
|
ATHS
|
Atherogenic Lipoprotein Phenotype
|
|
Alp
|
Arteriosclerosis
|
|
|
| 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
|
|
|
| Liver Cirrhosis |
|
Cirrhosis
|
Cirrhosis Of Liver
|
|
CIRRH
|
Cryptogenic Cirrhosis
|
|
Cirrhosis, Cryptogenic
|
Cirrhosis Nos
|
|
|
| Mandibular Hypoplasia, Deafness, Progeroid Features, And Lipodystrophy Syndrome |
|
Mdp Syndrome
|
Mandibular Hypoplasia-Deafness-Progeroid Syndrome
|
|
MDPL
|
Mdpl Syndrome
|
|
Mandibular Hypoplasia-Deafness-Progeroid Features-Lipodystrophy Syndrome
|
Mandibular Hypoplasia-Hearing Loss-Progeroid Syndrome
|
|
Lipodystrophy
|
Mandibular Hypoplasia, Deafness, Progeroid Features
|
|
Hypoplasia, Mandibular, Deafness, Progeroid Features, And Lipodystrophy Syndrome
|
Andibular Hypoplasia, Deafness, Progeroid Features, And Lipodystrophy Syndrome
|
|
|
| Hyperinsulinism |
|
|
| Acquired Metabolic Disease |
|
|
| 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
|
|
|
| Pre-Eclampsia |
|
Preeclampsia
|
Gestational Hypertension
|
|
Hypertension Induced By Pregnancy
|
Pre-Eclamptic Toxaemia
|
|
Pregnancy Associated Hypertension
|
Proteinuric Hypertension Of Pregnancy
|
|
Hypertension, Pregnancy-Induced, Susceptibility To
|
Preeclampsia/Eclampsia
|
|
Pregnancy Toxemia
|
Toxaemia Of Pregnancy
|
|
Gestational Proteinuric Hypertension
|
Pregnancy-Induced Hypertension
|
|
Toxemia Of Pregnancy
|
Preeclampsia, Susceptibility To
|
|
Transient Hypertension Of Pregnancy
|
Gestational [Pregnancy-Induced] Hypertension Without Significant Proteinuria
|
|
Gestational Hypertension Nos
|
Mild Proteinuric Hypertension Of Pregnancy
|
|
Pih - [Pregnancy-Induced Hypertension]
|
Pregnancy-Induced Hypertension Nos
|
|
Gestational [Pregnancy-Induced] Hypertension With Significant Proteinuria
|
Pe - [Pre-Eclampsia]
|
|
Pre-Eclampsia Nos
|
Pre-Eclamptic Nos
|
|
Pregnancy Pre-Eclampsia
|
Puerperal Pre-Eclampsia
|
|
Pre-Eclampsia Toxaemia
|
Toxaemia In Pregnancy
|
|
Pet - [Pre-Eclamptic Toxaemia]
|
Maternal Toxaemia
|
|
|
| Lipodystrophy, Familial Partial, Type 2 |
|
FPLD2
|
Lipoatrophic Diabetes
|
|
Familial Partial Lipodystrophy Type 2
|
Familial Partial Lipodystrophy, Dunnigan Type
|
|
Fpl2
|
Lipoatrophic Diabetes Mellitus
|
|
Lipodystrophy, Familial Partial, Dunnigan Type
|
Lipodystrophy, Familial, Of Limbs And Lower Trunk
|
|
Lipodystrophy, Reverse Partial
|
Familial Partial Lipodystrophy Dunnigan Type
|
|
Dunnigan Syndrome
|
Familial Lipodystrophy Of Limbs And Lower Trunk
|
|
Reverse Partial Lipodystrophy
|
Lipodystrophy, Familial Partial, 2
|
|
Generalized Lipoatrophy Associated With Diabetes, Hepatic Steatosis, Hypertrophic Cardiomyopathy And Leukomelanodermic Papules
|
Lipodystrophy Familial Of Limbs And Lower Trunk
|
|
Lipodystrophy Reverse Partial
|
Diabetes Mellitus, Lipoatrophic
|
|
Familial Partial Lipodystrophy, Type 2
|
Familial Generalized Lipodystrophy
|
|
|
| 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
|
|
|
| Familial Partial Lipodystrophy |
|
Lipodystrophy, Familial Partial
|
Fpld
|
|
Kobberling-Dunnigan Syndrome
|
Dunnigan Syndrome
|
|
Koberling-Dunnigan Syndrome
|
Dunnigan-Kobberling Syndrome
|
|
Fpl
|
Familial Partial Lipodystrophy, Type 2
|
|
|
| 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
|
|
|
| Pericarditis |
|
|
| Acromegaly |
|
Gigantism
|
Growth Hormone Excess
|
|
Pituitary Giant
|
Somatotroph Adenoma
|
|
Growth Hormone-Secreting Pituitary Adenoma
|
|
|
| Overnutrition |
|
|
| Familial Hyperlipidemia |
|
Familial Hyperlipoproteinemia
|
Hyperlipidaemia
|
|
Hyperlipoproteinemias
|
Hyperlipidemia
|
|
Hyperlipemia
|
Hyperlipidemias
|
|
|
| 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
|
|
|
| Congenital Generalized Lipodystrophy |
|
Berardinelli-Seip Congenital Lipodystrophy
|
Berardinelli-Seip Syndrome
|
|
Brunzell Syndrome
|
Bscl
|
|
Generalized Lipodystrophy
|
Lipodystrophy, Congenital Generalized
|
|
Seip Syndrome
|
Total Lipodystrophy
|
|
Cgl
|
Lipoatrophic Diabetes
|
|
Lipodystrophy, Generalized, Congenital
|
Familial Generalized Lipodystrophy
|
|
Congenital Generalized Lipodystrophy Type 2
|
Lipoatrophic Diabetes Mellitus
|
|
Familial Partial Lipodystrophy, Type 2
|
|
|
| Pellagra |
|
Niacin Deficiency
|
Niacin-Tryptophan Deficiency
|
|
Pellagroid Syndrome
|
|
|
| Carotid Stenosis |
|
Carotid Artery Stenosis
|
Stenosis, Carotid Artery
|
|
|
| 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
|
|
|
| Calcification Of Joints And Arteries |
|
Hereditary Arterial And Articular Multiple Calcification Syndrome
|
CALJA
|
|
Arterial Calcification Due To Cd73 Deficiency
|
Arterial Calcification Due To Deficiency Of Cd73
|
|
Acdc
|
Arterial Calcification And Distal Joint Calcification
|
|
Arterial Calcification Due To Deficiency Of Cd73:Acdc
|
Calcification Of Joints And Arteries
|
|
Calja
|
|
|
| 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
|
|
|
| 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
|
|
|
| Gastroesophageal Reflux |
|
Gastroesophageal Reflux Disease
|
Gerd
|
|
GER
|
Gastroesophageal Reflux, Pediatric
|
|
Acid Reflux
|
Gastresophageal Reflux
|
|
Gastro-Esophageal Reflux
|
Gerd - Gastro-Esophageal Reflux Disease
|
|
|
| Hypothyroidism |
|
Thyroid Diseases
|
Thyroid Disease
|
|
Thyroid Deficiency
|
Thyroid Insufficiency
|
|
Dysfunction Thyroid
|
Thyroid Dysfunction
|
|
|
| Hutchinson-Gilford Progeria Syndrome |
|
Progeria
|
HGPS
|
|
Hutchinson-Gilford Syndrome
|
Hutchinson-Gilford Progeria
|
|
Hutchinson Gilford Syndrome
|
Hutchinson Gilford Progeria Syndrome
|
|
Hutchinson-Gilford Disease
|
Progeria Of Childhood
|
|
Hutchinson-Gilford-Progeria Syndrome
|
|
|
| Hyperthyroidism |
|
|
| Nutritional Deficiency Disease |
|
Malnutrition
|
Nutritional Disorder
|
|
Nutritional Deficiency
|
Nutrition
|
|
Deficiency Diseases
|
Carbamoyl-Phosphate Synthase I Deficiency Disease
|
|
Nutrition Disorders
|
|
|
| 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
|
|
|
| Abdominal Obesity-Metabolic Syndrome Quantitative Trait Locus 2 |
|
Abdominal Obesity-Metabolic Syndrome
|
Abdominal Obesity Metabolic Syndrome
|
|
Metabolic Syndrome X
|
Aoms2
|
|
Aoms1
|
|
|
| Lipid Storage Disease |
|
Lipoidosis
|
Inborn Lipid Storage Disorder
|
|
Lipoid Storage Diseas
|
Lipid Storage Diseases
|
|
Lipidoses
|
|
|
| Ovarian Disease |
|
Ovarian Dysfunction
|
Ovarian Diseases
|
|
Ovarian Disorders
|
Disorder Of Endocrine Ovary
|
|
|
| Non-Alcoholic Steatohepatitis |
|
Nonalcoholic Steatohepatitis
|
Nash
|
|
Nash - [Non-Alcoholic Steatohepatitis]
|
Non-Alcoholic Steatohepatosis
|
|
|
| Conn'S Syndrome |
|
Cushing Syndrome
|
Hyperaldosteronism
|
|
Primary Hyperaldosteronism
|
Hypercortisolism
|
|
Primary Aldosteronism
|
Cushing'S Syndrome
|
|
Adrenal Gland Hyperfunction
|
Conn Syndrome
|
|
Hyperadrenalism
|
Ectopic Acth Syndrome
|
|
Hyperadrenocorticism
|
Cushing Disease
|
|
Cushing'S Disease
|
Adrenal Cortex Adenoma
|
|
Corticotroph Pituitary Adenoma
|
Pituitary Corticotroph Micro-Adenoma
|
|
Pituitary-Dependent Cushing Syndrome
|
Pituitary Acth Hypersecretion
|
|
Acth Syndrome, Ectopic
|
Acth-Secreting Pituitary Adenoma
|
|
Adrenal Hyperfunction Resulting From Pituitary Acth Excess
|
Ectopic Adrenocorticotropic Hormone Syndrome
|
|
Nodular Primary Adrenocortical Dysplasia
|
Pituitary Dependent Cushing Syndrome
|
|
Pituitary Cushing Syndrome
|
Pituitary-Dependant Cushing Syndrome
|
|
Pituitary-Dependant Hypercortisolism
|
Pituitary-Dependant Hypercortisolism Disorder
|
|
Aldosteronism Primary
|
Acth Syndrome Ectopic
|
|
Adrenal Cushing'S Syndrome
|
Adrenal Cortical Adenoma
|
|
Cushing Syndrome Nos
|
Cortisol Hypersecretion
|
|
Corticoadrenal Hypersecretion
|
Cushing Syndrome Secondary To Ectopic Acth-Secretion
|
|
Ectopic Cushing Syndrome
|
Hypercortisolism Due To Nonpituitary Tumour
|
|
Ectopic Acth - [Adrenocorticotropic Hormone] Secretion
|
Ectopic Acth - [Adrenocorticotropic Hormone] Secretion Causing Cushing Syndrome
|
|
Idiopathic Aldosteronism
|
Aldosteronism
|
|
Primary Aldosteronism Due To Bilateral Adrenal Hyperplasia
|
Primary Aldosteronism Due To Adrenal Hyperplasia
|
|
|
| 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
|
|
|
| Glucose Metabolism Disease |
|
Glucose Metabolism Disorders
|
Disorder Of Glucose Metabolism
|
|
|
| Nonobstructive Coronary Artery Disease |
|
Non-Cad
|
Non-Obstructive Coronary Artery Disease
|
|
|
| Adult Syndrome |
|
Acro-Dermato-Ungual-Lacrimal-Tooth Syndrome
|
Acro Dermato Ungual Lacrimal Tooth Syndrome
|
|
Pigment Anomaly-Ectrodactyly-Hypodontia Syndrome
|
Acro-Dermato-Ungual-Lacrimal-Tooth Syndrome
|
|
Adult
|
|
|
| Asthma |
|
Chronic Obstructive Asthma
|
Asthma, Diminished Response To Antileukotriene Treatment In
|
|
Bronchial Hyperreactivity
|
Asthma, Susceptibility To
|
|
Asthma, Bronchial
|
Asthma, Protection Against
|
|
Asthma, Nocturnal, Susceptibility To
|
Nocturnal Asthma
|
|
Asthma-Related Traits
|
Asthma-Related Traits, Susceptibility To
|
|
Asthma, Nocturnal
|
Chronic Obstructive Asthma With Acute Exacerbation
|
|
Chronic Obstructive Asthma With Status Asthmaticus
|
Exercise Induced Asthma
|
|
Exercise-Induced Asthma
|
Bronchial Asthma
|
|
Asthma, Exercise-Induced
|
Idiosyncratic Asthma
|
|
Unspecified Asthma With Acute Exacerbation
|
Asthma, Unspecified, With Stated Status Asthmaticus
|
|
Status Asthmaticus Nos
|
Acute Severe Asthma
|
|
Acute Severe Bronchial Asthma
|
Status Asthma
|
|
Status Post Asthmaticus
|
|
|
| Hypoglycemia |
|
Hypoglycaemia
|
Low Blood Sugar
|
|
Hypoglycaemia Nos
|
Spontaneous Hypoglycaemia
|
|
Nondiabetic Hypoglycaemia
|
Hypoglycaemic Disorder Nos
|
|
Hypoglycaemic Syndrome
|
|
|
| Prolactinoma |
|
Prolactin-Producing Pituitary Gland Adenoma
|
Prolactin-Secreting Pituitary Adenoma
|
|
Forbes-Albright Syndrome
|
Lactotroph Adenoma
|
|
Prl-Secreting Pituitary Adenoma
|
Prloma
|
|
Pituitary Lactotrophic Adenoma
|
Familial Prolactinoma
|
|
Pituitary Adenoma, Prolactin-Secreting
|
Prolactinoma Of Pituitary Gland
|
|
PSPA
|
|
|
| Complete Generalized Lipodystrophy |
|
|
| Inherited Metabolic Disorder |
|
Inborn Errors Of Metabolism
|
Inborn Metabolic Disorder
|
|
Inborn Metabolism Disorder
|
Metabolic Hereditary Disorder
|
|
Inborn Error Of Metabolism
|
Metabolism, Inborn Errors
|
|
|
| Endometrial Cancer |
|
Endometrial Carcinoma
|
Endometrial Neoplasm
|
|
Malignant Neoplasm Of Endometrium
|
Endometrioid Carcinoma
|
|
Endometrial Neoplasms
|
Carcinoma, Endometrioid
|
|
Endometrial Cancer, Familial
|
Endometrial Carcinoma, Somatic
|
|
Endometrial Cancer, Susceptibility To
|
Endometrial Ca
|
|
Malignant Endometrial Neoplasm
|
Neoplasm Of Endometrium
|
|
Primary Malignant Neoplasm Of Endometrium
|
Tumor Of Endometrium
|
|
Carcinoma Of The Endometrium
|
Endometrioid Carcinoma Of Female Reproductive System
|
|
ENDMC
|
Carcinoma Endometrioid
|
|
Endometrial Cancers
|
Cancer, Endometrial
|
|
Uterine Corpus Cancer
|
|
|
| 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
|
|
|
| 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
|
|
|
| Lipodystrophy, Congenital Generalized, Type 2 |
|
Congenital Generalized Lipodystrophy Type 2
|
CGL2
|
|
Berardinelli-Seip Congenital Lipodystrophy Type 2
|
Berardinelli-Seip Syndrome
|
|
Brunzell Syndrome Bscl2-Related
|
Total Lipodystrophy And Acromegaloid Gigantism
|
|
Berardinelli-Seip Congenital Lipodystrophy, Type 2
|
Seip Syndrome
|
|
Berardinelli Syndrome
|
Lipodystrophy, Total, And Acromegaloid Gigantism
|
|
Lipoatrophic Diabetes, Congenital
|
Lipodystrophy, Berardinelli-Seip Congenital, Type 2
|
|
Brunzell Syndrome, Bscl2-Related
|
Congenital Lipoatrophic Diabetes
|
|
Congenital Generalized Lipodystrophy 2
|
Lipoatrophic Diabetes
|
|
Lipodystrophy Berardinelli Type
|
Familial Generalized Lipodystrophy
|
|
Lipoatrophic Diabetes Mellitus
|
Familial Partial Lipodystrophy, Type 2
|
|
|
| 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]
|
|
|
| Placenta Disease |
|
Placenta Diseases
|
Placenta Disorder
|
|
Pregnancy Complications
|
Placenta Disorders
|
|
|
| Sleep Disorder |
|
Sleep Disorders
|
Non-Organic Sleep Disorder
|
|
|
| Rheumatoid Arthritis |
|
RA
|
Arthritis, Rheumatoid
|
|
Rheumatoid Arthritis, Susceptibility To
|
Arthritis Or Polyarthritis, Rheumatic
|
|
Atrophic Arthritis
|
Rheumatism Arthritis
|
|
Rheumatoid Polyarthritis
|
|
|
| Arterial Calcification Of Infancy |
|
Idiopathic Infantile Arterial Calcification
|
Generalized Arterial Calcification Of Infancy
|
|
Iiac
|
Occlusive Infantile Arteriopathy
|
|
Infantile Arteriosclerosis
|
Gaci
|
|
Idiopathic Obliterative Arteriopathy
|
Generalized Arterial Calcification In Infancy
|
|
Arteriopathia Calcificans Infantum
|
Diffuse Arterial Calcifying Elastopathy Of Infancy
|
|
Infantile Calcifying Arteriopathy
|
Medial Coronary Sclerosis Of Infancy
|
|
Coronary Sclerosis, Medial, Of Infancy
|
Calcification, Arterial, Generalized, Infancy
|
|
|
| Lysosomal Storage Disease |
|
Lysosomal Storage Diseases
|
Disorder Of Lysosomal Enzyme
|
|
Inborn Lysosomal Enzyme Disorder
|
Lysosomal Storage Metabolism Disorder
|
|
Lysosomal Storage Disorder
|
|
|
| Generalized Atherosclerosis |
|
Generalised Atherosclerosis
|
|
|
| Aromatase Excess Syndrome |
|
AEXS
|
Increased Aromatase Activity
|
|
Familial Hyperestrogenism
|
Hereditary Prepubertal Gynecomastia
|
|
Aromatase Activity, Increased
|
Familial Gynecomastia Due To Increased Aromatase Activity
|
|
Hereditary Gynecomastia
|
Gynecomastia, Familial
|
|
Familial Gynecomastia
|
|
|
| Pheochromocytoma |
|
Pheochromocytoma, Susceptibility To
|
Phaeochromocytoma
|
|
Adrenal Gland Chromaffin Paraganglioma
|
Adrenal Gland Chromaffinoma
|
|
Adrenal Gland Paraganglioma
|
Adrenal Gland Pheochromocytoma
|
|
Chromaffin Paraganglioma Of The Adrenal Gland
|
Intraadrenal Paraganglioma
|
|
PCC
|
Chromaffin Cell Tumor
|
|
Medullary Chromaffinoma
|
Medullary Paraganglioma
|
|
Pheochromoblastoma
|
Pheochromocytomas
|
|
Chromaffin Cell Neoplasm
|
Pheochromocytoma, Malignant
|
|
|
| Scoliosis |
|
|
| 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
|
|
|
| Psychotic Disorder |
|
Psychotic Disorders
|
Mental Or Behavioural Disorder
|
|
Psychotic
|
Mental Disorders
|
|
|
| Arteries, Anomalies Of |
|
Artery Disease
|
Arteriopathic Disease
|
|
|
| Inflammatory Bowel Disease |
|
Inflammatory Bowel Diseases
|
Bowel Disease, Inflammatory
|
|
|
| Autism Spectrum Disorder |
|
Asd
|
Autism Spectrum Disorders
|
|
Autistic Continuum
|
Pervasive Developmental Disorder
|
|
Pervasive Development Disorder
|
Autistic Behavior
|
|
Autistic Disorder
|
Autistic
|
|
Autistic Disorder Of Childhood Onset
|
Infantile Autism
|
|
Childhood Autism
|
Kanner Syndrome
|
|
Pervasive Developmental Delay Nos
|
Pervasive Developmental Disorder, Not Otherwise Specified
|
|
|
| Disorder Of Sexual Development |
|
Disorder Of Sex Development
|
Disorders Of Sex Development
|
|
Sex Development Disorder
|
Sex Differentiation Disease
|
|
Dsd
|
Sex Differentiation Disorders
|
|
|
| Schizophrenia |
|
SCZD
|
Schizophrenia With Or Without An Affective Disorder
|
|
Schizophrenia 12
|
Schizophrenia, Susceptibility To
|
|
Schizophrenia-1
|
Dementia Praecox
|
|
Schizophrenia 1
|
|
|
| Breast Cancer |
|
Breast Carcinoma
|
Male Breast Cancer
|
|
Breast Cancer, Familial
|
Malignant Neoplasm Of Breast
|
|
Breast Cancer, Susceptibility To
|
Breast Cancer, Early-Onset
|
|
Malignant Tumor Of Breast
|
Carcinoma Of Male Breast
|
|
Breast Cancer, Invasive Ductal
|
Breast Cancer, Protection Against
|
|
Breast Cancer, Somatic
|
Breast Cancer, Male
|
|
Breast Cancer, Lobular, Somatic
|
Breast Tumor
|
|
Mammary Cancer
|
Mammary Tumor
|
|
Malignant Neoplasm Of Male Breast
|
Mammary Carcinoma
|
|
Male Breast Carcinoma
|
Familial Cancer Of Breast
|
|
Invasive Ductal Breast Carcinoma
|
Breast Cancer Susceptibility
|
|
Breast Cancer, Male, Susceptibility To
|
Breast Cancer, Early-Onset, Susceptibility To
|
|
Malignant Tumor Of The Breast
|
Mammary Neoplasm
|
|
Primary Breast Cancer
|
Neoplasm Of Male Breast
|
|
Carcinoma Of Breast
|
Breast Cancer In Men
|
|
Familial Breast Cancer
|
Cancer Of Breast
|
|
BC
|
Breast Cancer Familial
|
|
Breast Cancer Familial Male
|
Breast Cancer, Familial Male
|
|
Breast Male Carcinoma
|
Breast Neoplasms
|
|
Breast Neoplasms, Male
|
Mammary Tumors
|
|
Mammary Carcinomas
|
Cancer, Breast
|
|
Cancer, Breast, Susceptibility
|
Invasive Breast Ductal Carcinoma
|
|
Breast Neoplasm
|
Susceptibility To Breast Cancer
|
|
Mammary Neoplasms
|
Animal Mammary Neoplasms
|
|
Primary Malignant Neoplasm Of Breast
|
Infiltrating Ductal Carcinoma Of Breast
|
|
Infiltrating Duct Carcinoma Of Unspecified Site
|
Infiltrating Ductular Carcinoma Of Unspecified Site
|
|
Invasive Breast Carcinoma Of No Special Type
|
Microinvasive Carcinoma Of Breast
|
|
Carcinoma With Apocrine Differentiation
|
|
|
| Autism |
|
Autistic Disorder
|
Autism Susceptibility 1
|
|
Childhood Autism
|
Autistic Disorder Of Childhood Onset
|
|
Infantile Autism
|
Kanner'S Syndrome
|
|
Autistic
|
|
|
| Connective Tissue Disease |
|
Connective Tissue Diseases
|
Connective Tissue Disorder
|
|
Abnormality Of Connective Tissue
|
Disorder Of Connective Tissue
|
|
Connective Tissue Disorders
|
|
|
| Nervous System Disease |
|
Abnormality Of The Nervous System
|
Nervous System Diseases
|
|
Nervous System Disorder
|
|
|
| Dilated Cardiomyopathy |
|
Familial Dilated Cardiomyopathy
|
Primary Dilated Cardiomyopathy
|
|
Idiopathic Dilated Cardiomyopathy
|
Congestive Cardiomyopathy
|
|
Idiopathic Dilation Cardiomyopathy
|
Primary Familial Dilated Cardiomyopathy
|
|
Cardiomyopathy, Dilated
|
DCM
|
|
Cardiomyopathy, Familial Dilated
|
Dilated Cardiomyopathy, Familial
|
|
Hypokinetic Dilated Cardiomyopathy, Familial
|
Familial Idiopathic Cardiomyopathy
|
|
Fdc
|
Cardiomyopathy, Familial Idiopathic
|
|
Idiopathic Cardiomegaly
|
Dilated Congestive Cardiomyopathy
|
|
Chronic Dilated Cardiomyopathy
|
Ccm - [Congestive Cardiomyopathy]
|
|
Cocm - [Congestive Cardiomyopathy]
|
Dcm - [Dilated Cardiomyopathy]
|
|
Dilated-Hypokinetic Cardiomyopathy
|
Congestive Idiopathic Cardiomyopathy
|
|
Primary Idiopathic Dilated Cardiomyopathy
|
|
|
