| Diseases |
Alias |
|
| Ehlers-Danlos Syndrome, Vascular Type |
|
Eds Iv
|
Eds4
|
|
Vascular Ehlers-Danlos Syndrome
|
Veds
|
|
Sack-Barabas Syndrome
|
EDSVASC
|
|
Ehlers-Danlos Syndrome, Type Iv, Autosomal Dominant
|
Vascular Type Ehlers-Danlos Syndrome
|
|
Arterial-Ecchymotic Eds
|
Ehlers-Danlos Syndrome Type 4
|
|
Vascular Eds
|
Ehlers-Danlos Syndrome, Type 4
|
|
Ehlers-Danlos Syndrome, Type Iv
|
Ehlers-Danlos Syndrome, Arterial Type
|
|
Ehlers-Danlos Syndrome, Ecchymotic Type
|
Ehlers-Danlos Syndrome, Sack-Barabas Type
|
|
Autosomal Dominant Type Iv Ehlers-Danlos Syndrome
|
Eds Type Iv
|
|
Eds Type 4
|
Ehlers Danlos Syndrome, Sack-Barabas Type
|
|
Ehlers Danlos Syndrome, Arterial Type
|
Ehlers Danlos Syndrome, Ecchymotic Type
|
|
Ehlers-Danlos Syndrome Type Iv
|
Ehlers-Danlos Syndrome 4
|
|
Ehlers-Danlos Syndrome Arterial Type
|
Ehlers-Danlos Syndrome Ecchymotic Type
|
|
Ehlers-Danlos Syndrome, Type 4 Variant
|
Ehlers-Danlos, Vascular Type Syndrome
|
|
|
| Polymicrogyria With Or Without Vascular-Type Ehlers-Danlos Syndrome |
|
PMGEDSV
|
Polymicrogyria With Or Without Vascular-Type Eds
|
|
Polymicrogyria Without Vascular-Type Ehlers-Danlos Syndrome
|
Polymicrogyria, With/Without Vascular-Type Eds
|
|
|
| Ehlers-Danlos Syndrome |
|
Eds
|
Cutis Hyperelastica
|
|
Elastic Skin
|
Ehlers-Danlos Syndromes
|
|
Ed Syndrome
|
Ehlers Danlos Syndrome
|
|
Ehlers Danlos Disease
|
Eds - [Ehlers-Danlos Syndrome]
|
|
|
| Acrogeria, Gottron Type |
|
Acrogeria
|
Metageria
|
|
Acrometageria
|
Gottron Syndrome
|
|
Familial Acrogeria
|
Gottron'S Syndrome
|
|
|
| Aortic Aneurysm, Familial Thoracic 4 |
|
AAT4
|
Faa4
|
|
Aortic Aneurysm/Aortic Dissection And Patent Ductus Arteriosus
|
Familial Aortic Aneurysm 4
|
|
Non-Syndromic Thoracic Aortic Aneurysms And Dissection
|
Taad
|
|
Thoracic Aortic Aneurysms And Dissection
|
Thoracic Aortic Aneurysms And Dissections
|
|
Aneurysm, Aortic, Thoracic, Familial, Type 4
|
|
|
| Aortic Aneurysm, Familial Thoracic 1 |
|
Thoracic Aortic Aneurysm
|
Annuloaortic Ectasia
|
|
Familial Thoracic Aortic Aneurysm And Aortic Dissection
|
Familial Aortic Dissection
|
|
Familial Taad
|
Familial Thoracic Aortic Aneurysm
|
|
Congenital Aneurysm Of Ascending Aorta
|
Familial Aortic Aneurysm
|
|
Familial Thoracic Aortic Aneurysm And Dissection
|
Aortic Aneurysm, Thoracic
|
|
AAT1
|
Faa1
|
|
Aortic Dissection, Familial
|
Aortic Aneurysm, Familial Thoracic
|
|
Aneurysm, Thoracic Aortic
|
Faa
|
|
Ftaad
|
Taa
|
|
Taad
|
Cystic Medial Necrosis Of Aorta
|
|
Familial Non-Syndromic Thoracic Aortic Aneurysm And Aortic Dissection
|
Aortic Aneurysm Thoracic
|
|
Familial Aortic Aneurysms
|
Aneurysm, Aortic, Thoracic, Familial, Type 1
|
|
Aneurysm Of Thoracic Aorta
|
Intrathoracic Aneurysm
|
|
Thoracic Aorta Aneurysm
|
Thoracic Aortic Aneurysm Without Rupture
|
|
Thoracic Aneurysm
|
Thorax Arterial Aneurysm
|
|
Thoracic Artery Aneurysm
|
Thoracic Arterial Aneurysm
|
|
Thorax Aneurysm
|
Thorax Aortic Aneurysm
|
|
Dissection Of Thoracic Aorta
|
|
|
| Familial Abdominal Aortic Aneurysm |
|
|
| Ehlers-Danlos Syndrome, Hypermobility Type |
|
Ehlers-Danlos Syndrome, Type 3
|
Ehlers-Danlos Syndrome, Type Iii
|
|
EDSHMB
|
Eds Iii
|
|
Benign Hypermobility Syndrome
|
Ehlers-Danlos Syndrome Hypermobility Type
|
|
Eds3
|
Type Iii Ehlers-Danlos Syndrome
|
|
Ehlers-Danlos Syndrome Type 3
|
Es-D3
|
|
|
| Aortic Dissection |
|
|
| Familial Cerebral Saccular Aneurysm |
|
Familial Berry Aneurysm
|
Familial Intracranial Saccular Aneurysm
|
|
|
| Loeys-Dietz Syndrome |
|
Loeys-Dietz Aortic Aneurysm Syndrome
|
Lds
|
|
Aortic Aneurysm Syndrome Due To Tgf-Beta Receptors Anomalies
|
Furlong Syndrome
|
|
|
| Hypermobile Ehlers-Danlos Syndrome |
|
Heds
|
Ehlers-Danlos Syndrome Type 3
|
|
Ehlers-Danlos Syndrome Hypermobility Type
|
Hypermobile Eds
|
|
Joint Hypermobility
|
Benign Joint Hypermobility Syndrome
|
|
Eds Hypermobility Type
|
Eds Type Iii
|
|
Ehlers-Danlos Syndrome Type Iii
|
Joint Hypermobility Syndrome
|
|
Eds3
|
Ehlers-Danlos Syndrome, Hypermobility Type
|
|
Eds Iii
|
Eds-Ht
|
|
|
| Lipoblastoma |
|
|
| Ehlers-Danlos Syndrome, Classic Type, 2 |
|
Ehlers-Danlos Syndrome, Type Ii
|
EDSCL2
|
|
Ehlers-Danlos Syndrome, Type Ii, Formerly
|
Eds2, Formerly
|
|
Ehlers Danlos Syndrome, Mild Classic Type, Formerly
|
Eds Ii, Formerly
|
|
Ehlers Danlos Syndrome, Mitis Type, Formerly
|
Ehlers-Danlos Syndrome Classic Type 2
|
|
Eds2
|
Eds Ii
|
|
Ehlers-Danlos Syndrome 2
|
Ehlers-Danlos Syndrome Mild Classic Type
|
|
Ehlers-Danlos Syndrome Mitis Type
|
Ehlers-Danlos, Classic Syndrome, Type 2
|
|
Ehlers-Danlos Syndrome Type 2
|
|
|
| Pelvic Organ Prolapse |
|
Rectal Prolapse
|
Pelvic Organ Prolapse, Susceptibility To, 1
|
|
Pelvic Organ Prolapse, Susceptibility To
|
Prolapse Of Vagina And Rectum
|
|
Vaginal Prolapse
|
Pelvic Organ Prolapse 1
|
|
Procidentia, Rectum
|
Prolapse Of Rectal Mucosa
|
|
Procidentia Of Rectum
|
Rectal Mucosa Prolapse
|
|
Rectum Prolapse
|
Procidentia Rectum
|
|
Rp - [Rectal Prolapse]
|
Male Proctocele
|
|
Male Rectocele
|
Proctoptosis
|
|
Female Genital Prolapse
|
Female Prolapse
|
|
Incompetence Of Pelvic Fundus
|
Relaxation Of Perineum
|
|
Deficiency Of Perineum
|
|
|
| Ehlers-Danlos Syndrome, Classic Type, 1 |
|
Ehlers-Danlos Syndrome, Type I
|
EDSCL1
|
|
Ehlers-Danlos Syndrome Classic Type 1
|
Ehlers-Danlos Syndrome Type 1
|
|
Ehlers-Danlos Syndrome, Type I, Formerly
|
Eds1, Formerly
|
|
Ehlers-Danlos Syndrome, Severe Classic Type, Formerly
|
Eds I, Formerly
|
|
Ehlers-Danlos Syndrome, Gravis Type, Formerly
|
Ehlers-Danlos Syndrome, Type 1
|
|
Type I Ehlers-Danlos Syndrome
|
Eds1
|
|
Eds I
|
Ehlers-Danlos Syndrome, Gravis Type
|
|
Ehlers-Danlos Syndrome, Severe Classic Type
|
Ehlers-Danlos Syndrome 1
|
|
Ehlers-Danlos, Classic Syndrome, Type 1
|
Ehlers-Danlos Syndrome Type 2
|
|
|
| Marfan Syndrome |
|
MFS
|
Mfs1
|
|
Marfan'S Syndrome
|
Marfan Syndrome Type 1
|
|
Marfan Syndrome, Type I
|
Mass Phenotype
|
|
Contractural Arachnodactyly
|
Mass Syndrome
|
|
Octd
|
Overlap Connective Tissue Disease
|
|
Marfanoid Hypermobility Syndrome
|
Marfan Disease
|
|
|
| Brittle Bone Disorder |
|
Osteogenesis Imperfecta
|
Brittle Bone Disease
|
|
Fragilitas Ossium
|
Osteopsathyrosis
|
|
Lobstein Disease
|
Oi
|
|
Vrolik Disease
|
Lobstein'S Disease
|
|
Lobstein'S Syndrome
|
Vrolik'S Disease
|
|
Porak And Durante Disease
|
Glass Bone Disease
|
|
Osteogenesis Imperfecta, Dominant Perinatal Lethal
|
Osteogenesis Imperfecta, Recessive Perinatal Lethal
|
|
Brittle Bone Syndrome
|
Oi - [Osteogenesis Imperfecta]
|
|
Ossium Fragility
|
Osteitis Fragilitans
|
|
Bony Fragility
|
Blue Sclera With Fragility Of Bone And Deafness
|
|
White Blue Sclera - Fragility Of Bone - Deafness
|
|
|
| Breast Scirrhous Carcinoma |
|
Infiltrating Carcinoma Of Breast With Fibrotic Stroma
|
Scirrhous Carcinoma Of Breast
|
|
|
| Collagen Disease |
|
Collagen Diseases
|
Collagen Disorder
|
|
|
| Hypermobility Syndrome |
|
Benign Joint Hypermobility
|
|
|
| Splenic Artery Aneurysm |
|
Aneurysm Of Splenic Artery
|
|
|
| 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
|
|
|
| Aortic Aneurysm |
|
Aortic Rupture
|
Thoracoabdominal Aortic Aneurysm, Ruptured
|
|
Ruptured Aortic Aneurysm
|
Aortic Aneurysms
|
|
Aortic Aneurysm Without Mention Of Rupture Nos
|
Ruptured Abdominal Aortic Aneurysm
|
|
Aortic Aneurysm, Ruptured
|
Ruptured Thoracic Aortic Aneurysm
|
|
|
| Connective Tissue Disease |
|
Connective Tissue Diseases
|
Connective Tissue Disorder
|
|
Abnormality Of Connective Tissue
|
Disorder Of Connective Tissue
|
|
Connective Tissue Disorders
|
|
|
| Varicose Veins |
|
Varices
|
Varix
|
|
Venous Ectasia
|
Venous Varices
|
|
Varicosity
|
|
|
| Polymicrogyria |
|
|
| Congenital Disorder Of Glycosylation, Type Iic |
|
CDG2C
|
Congenital Disorder Of Glycosylation Type Iic
|
|
Leukocyte Adhesion Deficiency Type Ii
|
Cdg Iic
|
|
Cdgiic
|
Rambam-Hasharon Syndrome
|
|
Leukocyte Adhesion Deficiency, Type Ii
|
Lad2
|
|
Leukocyte Adhesion Deficiency 2
|
Cdg-Iic
|
|
Congenital Disorder Of Glycosylation, Type 2c
|
Rhs
|
|
Cdg Syndrome Type Iic
|
Lad-Ii
|
|
Rambam Hasharon Syndrome
|
Congenital Disorder Of Glycosylation 2c
|
|
Glycosylation, Congenital Disorder Of, Type Iic
|
|
|
| Placenta Disease |
|
Placenta Diseases
|
Placenta Disorder
|
|
Pregnancy Complications
|
Placenta Disorders
|
|
|
| Carotid Artery Dissection |
|
Dissection Of Carotid Artery
|
|
|
| Hemopneumothorax |
|
|
| Arterial Tortuosity Syndrome |
|
Arterial Tortuosity
|
Ats
|
|
ATORS
|
Tortuosity, Arterial, Syndrome
|
|
|
| Pulsating Exophthalmos |
|
|
| Tricuspid Valve Prolapse |
|
|
| Plantar Fascial Fibromatosis |
|
Dupuytren'S Contracture Of Foot
|
Ledderhose'S Disease
|
|
Fibromatosis, Plantar
|
Ledderhose Disease
|
|
|
| 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
|
|
|
| Orthostatic Intolerance |
|
Mitral Valve Prolapse
|
Neurocirculatory Asthenia
|
|
Mitral Valve Prolapse Syndrome
|
Irritable Heart
|
|
Systolic Click-Murmur Syndrome
|
Soldiers Heart
|
|
Cardiovascular Malfunction Arising From Mental Factors
|
Cardiovascular Neurosis
|
|
Da Costa'S Syndrome
|
Krishaber'S Disease
|
|
Barlow'S Syndrome
|
Floppy Mitral Valve
|
|
Mitral Leaflet Syndrome
|
Myxomatous Mitral Valve Prolapse
|
|
Postural Orthostatic Tachycardia Syndrome Due To Net Deficiency
|
Familial Orthostatic Tachycardia Due To Norepinephrine Transporter Deficiency
|
|
Orthostatic Intolerance Due To Net Deficiency
|
Pots Due To Net Deficiency
|
|
OI
|
Intolerance, Orthostatic
|
|
Mitral Valve Prolapse, Familial, X-Linked
|
Ballooning Mitral Valve
|
|
Barlow Syndrome
|
Flail Mitral Leaflet
|
|
Myxomatous Mitral Valve
|
Mitral Valve Prolapse-Click Syndrome
|
|
Prolapsing Mitral Valve Leaflet Syndrome
|
Billowing Mitral Valve Leaflet
|
|
Posterior Mitral Leaflet Deformity
|
Ballooning Posterior Leaflet Syndrome
|
|
Blue Valve Syndrome
|
Floppy Mitral Valve Syndrome
|
|
Mitral Valvular Prolapse
|
Systolic Click Syndrome
|
|
|
| Stickler Syndrome, Type I |
|
Stickler Syndrome 1
|
Stickler Syndrome Type 1
|
|
STL1
|
Aom
|
|
Stickler Syndrome, Type 1
|
Stickler Syndrome, Vitreous Type 1
|
|
Stickler Syndrome, Membranous Vitreous Type
|
Arthroophthalmopathy, Hereditary Progressive
|
|
Arthro-Ophthalmopathy Hereditary Progressive
|
Stickler Syndrome Membranous Vitreous Type
|
|
Stickler Syndrome Type I
|
Stickler Syndrome Vitreous Type 1
|
|
|
| Prolapse Of Urethra |
|
|
| Aortic Disease |
|
Aortic Diseases
|
Aortic Disorder
|
|
Disorder Of The Aorta
|
|
|
| Loeys-Dietz Syndrome 1 |
|
Furlong Syndrome
|
Loeys-Dietz Aortic Aneurysm Syndrome
|
|
LDS1
|
Aat5
|
|
Loeys-Dietz Syndrome Type 1
|
Aortic Aneurysm, Familial Thoracic 5
|
|
Familial Throacic Aortic Aneurysm 5
|
Loeys-Dietz Syndrome
|
|
Aortic Aneurysm Syndrome, Loeys-Dietz Type
|
Familial Thoracic Aortic Aneurysm 5
|
|
Ldas
|
Marfanoid Disorder-Craniosynostosis Syndrome
|
|
Aneurysm, Aortic, Thoracic, Familial, Type 5
|
Loeys-Dietz Syndrome, Type 1
|
|
Loeys-Dietz Syndrome, Type 2a
|
|
|
| Amebiasis |
|
Amoebiasis
|
Entamoebiasis
|
|
Chronic Intestinal Amebiasis
|
Amoebiasis, Unspecified
|
|
Amebic Colitis
|
Amoebic Enteritis
|
|
Infection Due To Entamoeba Histolytica
|
Amoebic Infection
|
|
Disease Due To Endamoebidae
|
Amoebiasis Nos
|
|
|
| Cerebral Arterial Disease |
|
Cerebral Arterial Diseases
|
|
|
| Cerebral Arteriopathy, Autosomal Dominant, With Subcortical Infarcts And Leukoencephalopathy, Type 2 |
|
CADASIL2
|
Cadasil 2
|
|
Autosomal Dominant Cerebral Arteriopathy With Subcortical Infarcts And Leukoencephalopathy Type 2
|
Htra1-Related Autosomal Dominant Cerebral Small Vessel Disease
|
|
Htra1-Related Autosomal Dominant Cerebral Angiopathy
|
Cerebral Arteriopathy, Autosomal Dominant, With Subcortical Infarcts And Leukoencephalopathy, 2
|
|
Cerebral Arteriopathy With Subcortical Infarcts And Leukoencephalopathy, Autosomal Dominant, 2
|
|
|
| Inguinal Hernia |
|
Hernia Inguinal
|
Hernia, Inguinal
|
|
Inguinal Hernias
|
Bubonocele
|
|
Indirect Inguinal Hernia
|
Direct Inguinal Hernia
|
|
Oblique Inguinal Hernia
|
Scrotal Hernia
|
|
Ih - [Inguinal Hernia]
|
|
|
| Bethlem Myopathy 1 |
|
Bethlem Myopathy
|
Myopathy, Benign Congenital, With Contractures
|
|
Muscular Dystrophy, Benign Congenital
|
BTHLM1
|
|
Muscular Dystrophy, Limb-Girdle, Autosomal Dominant 5
|
Lgmdd5
|
|
Benign Congenital Muscular Dystrophy
|
Benign Autosomal Dominant Myopathy
|
|
Myopathy, Bethlem
|
Myopathy, Bethlem, Type 1
|
|
|
| Aortic Aneurysm, Familial Abdominal, 1 |
|
Abdominal Aortic Aneurysm
|
Aortic Aneurysm, Familial Abdominal 1
|
|
Aneurysm, Abdominal Aortic
|
AAA
|
|
Aortic Aneurysm, Abdominal
|
AAA1
|
|
Aortic Aneurysm, Familial Abdominal
|
Aortic Aneurysm Abdominal
|
|
Abdominal Aortic Aneurysms
|
Abdominal Aortic Aneurysm Without Mention Of Perforation Or Rupture
|
|
Abdomen Aneurysm
|
Abdominal Aorta Aneurysm
|
|
Aneurysm Of Abdominal Aorta
|
Aortic Abdomen Aneurysm
|
|
Aaa - [Abdominal Aortic Aneurysm]
|
Abdominal Aneurysm
|
|
Abdominal Aorta Aneurysm Rupture
|
Abdominal Aorta Aneurysm Ruptured
|
|
Abdominal Aortic Aneurysm Which Has Ruptured
|
Ruptured Aaa
|
|
Abdomen Aorta Aneurysm Ruptured
|
Abdomen Aorta Rupture
|
|
Abdomen Aortic Aneurysm Rupture
|
Abdomen Aneurysm Rupture
|
|
Abdomen Aortic Aneurysm Ruptured
|
Abdomen Aortic Rupture
|
|
Abdominal Aorta Rupture
|
Abdominal Aortic Rupture
|
|
Rupture Abdomen Aorta Aneurysm
|
Rupture Abdominal Aortic Aneurysm
|
|
Ruptured Abdomen Aneurysm
|
Ruptured Abdomen Aorta
|
|
Ruptured Abdomen Aortic
|
Ruptured Abdominal Aneurysm
|
|
Ruptured Abdominal Aorta
|
Ruptured Abdominal Aortic
|
|
Ruptured Aorta Abdominalis Aneurysm
|
False Abdomen Aorta Aneurysm Ruptured
|
|
False Abdominal Aortic Aneurysm Ruptured
|
False Abdominal Aorta Aneurysm Ruptured
|
|
False Abdomen Aortic Aneurysm Ruptured
|
|
|
| Stickler Syndrome |
|
Arthroophthalmopathy
|
Hereditary Arthro-Ophthalmo-Dystrophy
|
|
Hereditary Arthro-Ophthalmopathy
|
Stickler Dysplasia
|
|
Hereditary Progressive Arthroophthalmopathy
|
Stickler Syndrome, Type 1
|
|
|
| Interstitial Lung Disease 2 |
|
Idiopathic Pulmonary Fibrosis
|
Ipf
|
|
Fibrocystic Pulmonary Dysplasia
|
Pulmonary Fibrosis, Idiopathic
|
|
Pulmonary Fibrosis, Idiopathic, Susceptibility To
|
Cryptogenic Fibrosing Alveolitis
|
|
ILD2
|
Idiopathic Pulmonary Fibrosis, Familial
|
|
Fibrosing Alveolitis, Cryptogenic
|
Uip
|
|
Fibrosing Alveolitis
|
Interstitial Pneumonitis, Usual
|
|
Familial Idiopathic Pulmonary Fibrosis
|
Idiopathic Fibrosing Alveolitis, Chronic Form
|
|
Usual Interstitial Pneumonia
|
Fibrosing Alveolitis Cryptogenic
|
|
Hamman-Rich Disease
|
Idiopathic Pulmonary Fibrosis Familial
|
|
Interstitial Pneumonitis Usual
|
Fibrosis Idiopathic Pulmonary
|
|
Fibrosis, Pulmonary, Idiopathic
|
Hamman-Rich Syndrome
|
|
Chronic Idiopathic Pulmonary Fibrosis
|
Acute Interstitial Pneumonia
|
|
Interstitial Pulmonary Fibrosis
|
Ipf - [Idiopathic Pulmonary Fibrosis]
|
|
Idiopathic Lung Fibrosis
|
Fibrosing Lung Disease
|
|
Pulmonary Fibrosis Nos
|
Fibrosing Pneumonitis
|
|
|
| Osteochondrodysplasia |
|
Skeletal Dysplasia
|
Chondrodystrophy
|
|
Congenital Anomaly Of Cartilage
|
Osteochondrodysplasias
|
|
Cartilage Development Disorder
|
Osteochondrodysplasia Syndrome
|
|
Dysplasia, Skeletal
|
Mucopolysaccharidosis Iv
|
|
|
| Patent Ductus Arteriosus 1 |
|
Patent Ductus Arteriosus
|
PDA1
|
|
Pda
|
Ductus Arteriosus, Patent
|
|
Patent Ductus Arteriosus, Susceptibility To
|
Patent Ductus Botalli
|
|
Patency Of The Ductus Arteriosus
|
Patent Ductus Arteriosus Familial
|
|
Ductus Arteriosus Patent
|
Patent Ductus Arteriosus - Persisting Type
|
|
|
| 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
|
|
|
| Williams-Beuren Syndrome |
|
Williams Syndrome
|
WBS
|
|
Wms
|
Deletion 7q11.23
|
|
Monosomy 7q11.23
|
Chromosome 7q11.23 Deletion Syndrome, 1.5- To 1.8-Mb
|
|
Fanconi Schlesinger Syndrome
|
Beuren Syndrome
|
|
Elfin Facies Syndrome
|
Elfin Facies With Hypercalcemia
|
|
Hypercalcemia-Supravalvar Aortic Stenosis
|
Ws
|
|
|
| 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
|
|
|
| Hypertrophic Cardiomyopathy |
|
Hypertrophic Obstructive Cardiomyopathy
|
Cardiomyopathy, Hypertrophic
|
|
Cardiomyopathy Hypertrophic Obstructive
|
Cardiomyopathy, Hypertrophic, Familial
|
|
Idiopathic Myocardial Hypertrophy
|
Idiopathic Hypertrophic Cardiomyopathy
|
|
Obstructive Idiopathic Hypertrophic Cardiomyopathy
|
Obstructive Cardiomyopathy
|
|
Idiopathic Hypertrophic Subaortic Stenosis
|
Muscular Subaortic Stenosis
|
|
Hypertrophic Obstructive Subaortic Stenosis
|
|
|
