| 疾病名称 |
别名 |
|
| Andersen Cardiodysrhythmic Periodic Paralysis |
|
Andersen Syndrome
|
Andersen-Tawil Syndrome
|
|
LQT7
|
Long Qt Syndrome 7
|
|
Ats
|
Periodic Paralysis, Potassium-Sensitive Cardiodysrhythmic Type
|
|
Long Qt Syndrome Type 7
|
Andersen Tawil Syndrome
|
|
Potassium-Sensitive Cardiodysrhythmic Type
|
Lqts Type 7
|
|
Long Qt Syndrome-7
|
|
|
| Short Qt Syndrome 3 |
|
SQT3
|
Short Qt Syndrome Type 3
|
|
Short Qt Syndrome-3
|
|
|
| Atrial Fibrillation, Familial, 9 |
|
ATFB9
|
Fibrillation, Atrial, Familial, Type 9
|
|
|
| Glycogen Storage Disease Iv |
|
Gsd Iv
|
Glycogen Branching Enzyme Deficiency
|
|
Andersen Disease
|
Amylopectinosis
|
|
Glycogen Storage Disease Type Iv
|
GSD4
|
|
Brancher Deficiency
|
Glycogen Storage Disease, Type Iv
|
|
Glycogen Storage Disease Due To Glycogen Branching Enzyme Deficiency, Congenital Neuromuscular Form
|
Gbe1 Deficiency
|
|
Glycogenosis Iv
|
Cirrhosis, Familial, With Deposition Of Abnormal Glycogen
|
|
Glycogen Storage Disease Type 4
|
Glycogenosis 4
|
|
Potassium-Sensitive Periodic Paralysis, Ventricular Ectopy, And Dysmorphic Features
|
Andersen'S Disease
|
|
Glycogen Storage Disease Due To Glycogen Branching Enzyme Deficiency, Childhood Neuromuscular Form
|
Glycogen Storage Disease Due To Glycogen Branching Enzyme Deficiency, Fatal Perinatal Neuromuscular Form
|
|
Brancher Deficiency Glycogenosis
|
Branching-Transferase Deficiency Glycogenosis
|
|
Deficiency Of 1,4-Alpha-Glucan Branching Enzyme
|
Andersen-Tawil Syndrome
|
|
Gsd 4
|
Andersen Cardiodysrhythmic Periodic Paralysis
|
|
Lqt7
|
Long Qt Syndrome 7
|
|
Periodic Paralysis, Potassium-Sensitive Cardiodysrhythmic Type
|
Andersen Glycogenosis
|
|
Branching Enzyme Deficiency
|
Glycogenosis, Type Iv
|
|
Gsd Type Iv
|
Type Iv Glycogenosis
|
|
Gbe Deficiency, Childhood Neuromuscular Form
|
Gsd Due To Glycogen Branching Enzyme Deficiency, Childhood Neuromuscular Form
|
|
Gsd Type 4, Childhood Neuromuscular Form
|
Gsdiv, Childhood Neuromuscular Form
|
|
Glycogen Storage Disease Type 4, Childhood Neuromuscular Form
|
Glycogen Storage Disease Type Iv, Childhood Neuromuscular Form
|
|
Glycogenosis Due To Glycogen Branching Enzyme Deficiency, Childhood Neuromuscular Form
|
Glycogenosis Type 4, Childhood Neuromuscular Form
|
|
Glycogenosis Type Iv, Childhood Neuromuscular Form
|
Glycogen Storage Disease Due To Glycogen Branching Enzyme Deficiency, Adult Neuromuscular Form
|
|
Gbe Deficiency, Adult Neuromuscular Form
|
Gsd Due To Glycogen Branching Enzyme Deficiency, Adult Neuromuscular Form
|
|
Gsd Type 4, Adult Neuromuscular Form
|
Gsdiv, Adult Neuromuscular Form
|
|
Glycogen Storage Disease Type 4, Adult Neuromuscular Form
|
Glycogen Storage Disease Type Iv, Adult Neuromuscular Form
|
|
Glycogenosis Due To Glycogen Branching Enzyme Deficiency, Adult Neuromuscular Form
|
Glycogenosis Type 4, Adult Neuromuscular Form
|
|
Glycogenosis Type Iv, Adult Neuromuscular Form
|
Gbe Deficiency, Congenital Neuromuscular Form
|
|
Gsd Due To Glycogen Branching Enzyme Deficiency, Congenital Neuromuscular Form
|
Gsd Type 4, Congenital Neuromuscular Form
|
|
Gsdiv, Congenital Neuromuscular Form
|
Glycogen Storage Disease Type 4, Congenital Neuromuscular Form
|
|
Glycogen Storage Disease Type Iv, Congenital Neuromuscular Form
|
Glycogenosis Due To Glycogen Branching Enzyme Deficiency, Congenital Neuromuscular Form
|
|
Glycogenosis Type 4, Congenital Neuromuscular Form
|
Glycogenosis Type Iv, Congenital Neuromuscular Form
|
|
Glycogen Storage Disease Due To Glycogen Branching Enzyme Deficiency, Childhood Combined Hepatic And Myopathic Form
|
Gbe Deficiency, Childhood Combined Hepatic And Myopathic Form
|
|
Gsd Due To Glycogen Branching Enzyme Deficiency, Childhood Combined Hepatic And Myopathic Form
|
Gsd Type 4, Childhood Combined Hepatic And Myopathic Form
|
|
Gsdiv, Childhood Combined Hepatic And Myopathic Form
|
Glycogen Storage Disease Type 4, Childhood Combined Hepatic And Myopathic Form
|
|
Glycogen Storage Disease Type Iv, Childhood Combined Hepatic And Myopathic Form
|
Glycogenosis Due To Glycogen Branching Enzyme Deficiency, Childhood Combined Hepatic And Myopathic Form
|
|
Glycogenosis Type 4, Childhood Combined Hepatic And Myopathic Form
|
Glycogenosis Type Iv, Childhood Combined Hepatic And Myopathic Form
|
|
Gbe Deficiency, Fatal Perinatal Neuromuscular Form
|
Gsd Due To Glycogen Branching Enzyme Deficiency, Fatal Perinatal Neuromuscular Form
|
|
Gsd Type 4, Fatal Perinatal Neuromuscular Form
|
Gsdiv, Fatal Perinatal Neuromuscular Form
|
|
Glycogen Storage Disease Type 4, Fatal Perinatal Neuromuscular Form
|
Glycogen Storage Disease Type Iv, Fatal Perinatal Neuromuscular Form
|
|
Glycogenosis Due To Glycogen Branching Enzyme Deficiency, Fatal Perinatal Neuromuscular Form
|
Glycogenosis Type 4, Fatal Perinatal Neuromuscular Form
|
|
Glycogenosis Type Iv, Fatal Perinatal Neuromuscular Form
|
Glycogen Storage Disease Due To Glycogen Branching Enzyme Deficiency, Non Progressive Hepatic Form
|
|
Gbe Deficiency, Non Progressive Hepatic Form
|
Gsd Due To Glycogen Branching Enzyme Deficiency, Non Progressive Hepatic Form
|
|
Gsd Type 4, Non Progressive Hepatic Form
|
Gsdiv, Non Progressive Hepatic Form
|
|
Glycogen Storage Disease Type 4, Non Progressive Hepatic Form
|
Glycogen Storage Disease Type Iv, Non Progressive Hepatic Form
|
|
Glycogenosis Due To Glycogen Branching Enzyme Deficiency, Non Progressive Hepatic Form
|
Glycogenosis Type 4, Non Progressive Hepatic Form
|
|
Glycogenosis Type Iv, Non Progressive Hepatic Form
|
Glycogen Storage Disease Due To Glycogen Branching Enzyme Deficiency, Progressive Hepatic Form
|
|
Gbe Deficiency, Progressive Hepatic Form
|
Gsd Due To Glycogen Branching Enzyme Deficiency, Progressive Hepatic Form
|
|
Gsd Type 4, Progressive Hepatic Form
|
Gsdiv, Progressive Hepatic Form
|
|
Glycogen Storage Disease Type 4, Progressive Hepatic Form
|
Glycogen Storage Disease Type Iv, Progressive Hepatic Form
|
|
Glycogenosis Due To Glycogen Branching Enzyme Deficiency, Progressive Hepatic Form
|
Glycogenosis Type 4, Progressive Hepatic Form
|
|
Glycogenosis Type Iv, Progressive Hepatic Form
|
Glycogen Storage Disease 4
|
|
Gsd-Iv
|
Storage Disease, Glycogen, Type Iv
|
|
|
| Familial Short Qt Syndrome |
|
Sqts
|
Genetic Short Qt Syndrome
|
|
|
| Familial Atrial Fibrillation |
|
Atrial Fibrillation, Familial
|
Atfb
|
|
Atrial Fibrillation Autosomal Dominant
|
Autosomal Dominant Atrial Fibrillation
|
|
Auricular Fibrillation
|
Atrial Fibrillation
|
|
Atrial Fibrillation, Familial, 1
|
|
|
| Periodic Paralysis |
|
Westphal Disease
|
Periodic Myotonia
|
|
Myoplegic Dystrophy
|
Familial Recurrent Paralysis
|
|
Familial Myoplegia
|
Cavare Disease
|
|
Cavarre Disease
|
Familial Paralysis
|
|
Familial Periodic Paralysis
|
Myotonic Periodic Paralysis
|
|
|
| Short Qt Syndrome |
|
Sqts
|
Familial Short Qt Syndrome
|
|
|
| Atrial Fibrillation |
|
A-Fib
|
Fibrillation, Atrial
|
|
Af - [Atrial Fibrillation]
|
Rapid Atrial Fibrillation
|
|
A Fib - [Atrial Fibrillation]
|
|
|
| Catecholaminergic Polymorphic Ventricular Tachycardia |
|
Cpvt
|
Catecholamine-Induced Polymorphic Ventricular Tachycardia
|
|
Familial Polymorphic Ventricular Tachycardia
|
Malignant Paroxysmal Ventricular Tachycardia
|
|
Multifocal Ventricular Premature Beats
|
Stress-Induced Polymorphic Ventricular Tachycardia
|
|
Bidirectional Tachycardia Induced By Catecholamine
|
Double Tachycardia Induced By Catecholamines
|
|
Polymorphic Catecholergic Ventricular Tachycardia
|
Syncopal Paroxysmal Tachycardia
|
|
Bidirectional Tachycardia Induced By Catecholamines
|
Fpvt
|
|
Bidirectional Ventricular Tachycardia Induced By Catecholamine
|
Polymorphic Ventricular Tachycardia Induced By Catecholamines
|
|
Ventricular Tachycardia, Catecholaminergic Polymorphic
|
Ventricular Tachycardia, Catecholaminergic Polymorphic, 1
|
|
Familial Ventricular Tachycardia
|
Multifocal Pvcs
|
|
Multifocal Premature Ventricular Beats
|
|
|
| Long Qt Syndrome |
|
Romano-Ward Syndrome
|
Long Q-T Syndrome
|
|
Lqt
|
Qt Syndrome, Long
|
|
Congenital Long Qt Syndrome
|
Familial Long Qt Syndrome
|
|
|
| Cardiac Arrhythmia, Ankyrin-B-Related |
|
Long Qt Syndrome 4
|
Ankyrin-B Syndrome
|
|
LQT4
|
Ankyrin-B-Related Cardiac Arrhythmia
|
|
Sick Sinus Syndrome With Bradycardia
|
Arrhythmia, Cardiac, Ankyrin B-Related
|
|
|
| Campomelic Dysplasia |
|
Acampomelic Campomelic Dysplasia
|
Camptomelic Dysplasia
|
|
Campomelic Dysplasia With Autosomal Sex Reversal
|
Cmpd
|
|
CMD1
|
Cmpd1
|
|
Cmpd1/Sra1
|
Acampomelic Campomelic Dysplasia With Autosomal Sex Reversal
|
|
Campomelic Dwarfism
|
Campomelic Syndrome
|
|
Dysplasia, Campomelic
|
Chronic Myeloproliferative Disorder
|
|
Familial Dilated Cardiomyopathy
|
|
|
| Ventricular Tachycardia, Catecholaminergic Polymorphic, 3 |
|
Catecholaminergic Polymorphic Ventricular Tachycardia 3
|
CPVT3
|
|
Cvpt3
|
Tachycardia, Ventricular, Catecholaminergic Polymorphic, Type 3
|
|
|
| Myasthenic Syndrome, Congenital, 20, Presynaptic |
|
Congenital Myasthenic Syndrome 20
|
CMS20
|
|
Congenital Myasthenic Syndrome 20 Presynaptic
|
Myasthenic Syndrome, Congenital, Type 20, Presynaptic
|
|
|
| Timothy Syndrome |
|
Long Qt Syndrome With Syndactyly
|
TS
|
|
Lqt8
|
Long Qt Syndrome 8
|
|
Long Qt Syndrome Type 8
|
Long Qt Syndrome-Syndactyly Syndrome
|
|
|
| Familial Periodic Paralysis |
|
Genetic Periodic Paralysis
|
Paralyses, Familial Periodic
|
|
|
| Hyperkalemic Periodic Paralysis |
|
HYPP
|
Gamstorp Disease
|
|
Gamstorp Episodic Adynamy
|
Adynamia Episodica Hereditaria With Or Without Myotonia
|
|
Familial Hyperkalemic Periodic Paralysis
|
Hyperkpp
|
|
Hyperpp
|
Adynamia Episodica Hereditaria
|
|
Primary Hyperkalemic Periodic Paralysis
|
Hyperkalemic Periodic Paralysis, Type 2
|
|
Sodium Channel Muscle Disease
|
Familial Hyperpp
|
|
Hyperkalemic Pp
|
Primary Hyperpp
|
|
Periodic Paralysis Hyperkalemic
|
Periodic Paralysis Normokalemic
|
|
NKPP
|
Periodic Paralysis Eukalemic
|
|
Paralysis, Hyperkalemic Periodic
|
Paralysis, Periodic, Hyperkalemic
|
|
Potassium Aggravated Myotonia
|
|
|
| Long Qt Syndrome 6 |
|
LQT6
|
Long Qt Syndrome 3/6
|
|
Lqt3/6
|
Susceptibility To Acquired Long Qt Syndrome 6
|
|
Long Qt Syndrome-6
|
Long Qt Syndrome 6, Acquired, Susceptibility To
|
|
Qt Syndrome, Long, Type 6
|
Long Qt Syndrome 3-6
|
|
|
| Long Qt Syndrome 2 |
|
LQT2
|
Long Qt Syndrome, Acquired, Reduced Susceptibility To
|
|
Long Qt Syndrome 1/2
|
Long Qt Syndrome 2/3
|
|
Long Qt Syndrome 2/5
|
Long Qt Syndrome 2, Acquired, Susceptibility To
|
|
Long Qt Syndrome, Acquired, Reduced
|
Long Qt Syndrome Type 2
|
|
Long Qt Syndrome 2/9
|
Lqt1/2
|
|
Lqt2/3
|
Lqt2/5
|
|
Lqt2/9
|
Susceptibility To Acquired Long Qt Syndrome 2
|
|
Long Qt Syndrome-2
|
Qt Syndrome, Long, Type 2
|
|
Long Qt Syndrome 1-2
|
Long Qt Syndrome 2-3
|
|
Long Qt Syndrome 2-5
|
Long Qt Syndrome 9
|
|
|
| Paramyotonia Congenita Of Von Eulenburg |
|
Paramyotonia Congenita
|
PMC
|
|
Paralysis Periodica Paramyotonica
|
Eulenburg Disease
|
|
Myotonia Congenita Intermittens
|
Von Eulenburg Paramyotonia Congenita
|
|
Paralysis Periodica Paramyotonia
|
Von Eulenberg'S Disease
|
|
Paramyotonia Congenita Without Cold Paralysis
|
Eulenburg Syndrome
|
|
Paramyotonia
|
|
|
| Long Qt Syndrome 13 |
|
LQT13
|
Qt Syndrome, Long, Type 13
|
|
|
| Long Qt Syndrome 5 |
|
LQT5
|
Long Qt Syndrome 2/5
|
|
Lqt2/5
|
Susceptibility To Acquired Long Qt Syndrome 5
|
|
Long Qt Syndrome-5
|
Long Qt Syndrome 5, Acquired, Susceptibility To
|
|
Qt Syndrome, Long, Type 5
|
Long Qt Syndrome 2-5
|
|
|
| Long Qt Syndrome 3 |
|
LQT3
|
Long Qt Syndrome Type 3
|
|
Long Qt Syndrome-3
|
Qt Syndrome, Long, Type 3
|
|
|
| Long Qt Syndrome 14 |
|
LQT14
|
Long Qt Syndrome, Type 14
|
|
|
| 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
|
|
|
| Long Qt Syndrome 15 |
|
LQT15
|
Long Qt Syndrome, Type 15
|
|
|
| Long Qt Syndrome 10 |
|
LQT10
|
Atrial Fibrillation, Familial, 17
|
|
ATFB17
|
Long Qt Syndrome-10
|
|
Qt Syndrome, Long, Type 10
|
|
|
| Long Qt Syndrome 9 |
|
LQT9
|
Long Qt Syndrome-9
|
|
Qt Syndrome, Long, Type 9
|
|
|
| Hypokalemic Periodic Paralysis, Type 1 |
|
Hypokalemic Periodic Paralysis
|
Hokpp
|
|
Hypopp
|
Westphall Disease
|
|
HOKPP1
|
Familial Hypokalemic Periodic Paralysis
|
|
Familial Periodic Paralysis
|
Westphal Disease
|
|
Hypokalemic Periodic Paralysis Type 1
|
Hypokalemic Familial Periodic Paralysis
|
|
Periodic Hypokalemic Paralysis
|
Periodic Paralysis I
|
|
Hypokpp
|
Primary Hypokalemic Periodic Paralysis
|
|
Periodic Paralysis Hypokalemic 1
|
Paralysis, Hypokalemic, Periodic
|
|
Paralysis, Hypokalemic, Periodic, Type 1
|
|
|
| Long Qt Syndrome 11 |
|
LQT11
|
Long Qt Syndrome-11
|
|
Qt Syndrome, Long, Type 11
|
|
|
| Congestive Heart Failure |
|
Congestive Heart Disease
|
Heart Failure
|
|
Cardiac Failure Congestive
|
Chf
|
|
Weak Heart
|
Heart Failure Congestive
|
|
Ccf - [Congestive Cardiac Failure]
|
Chf - [Congestive Heart Failure]
|
|
Congestive Cardiac Diseases
|
Congested Heart Failure
|
|
Congestive Cardiac Failure
|
Cardiac Anasarca
|
|
Cardiac Oedema
|
Cardiac Stasis
|
|
Cardiovascular Oedema
|
Cardiac Hydrops
|
|
Congestive Failure
|
Heart Congestion
|
|
Heart Fluid
|
Oedematous Heart
|
|
|
| Long Qt Syndrome 12 |
|
LQT12
|
Qt Syndrome, Long, Type 12
|
|
|
| Myotonia Congenita |
|
Congenital Myotonia, Autosomal Dominant Form
|
Congenital Myotonia
|
|
Thomsen And Becker Disease
|
Thomsen Disease
|
|
Thomsen'S Disease
|
Generalized Myotonia Of Thomsen
|
|
Congenital Myotonic Muscular Dystrophy
|
Myotonia Congenita Nos
|
|
|
| Jervell And Lange-Nielsen Syndrome 1 |
|
Jervell And Lange-Nielsen Syndrome
|
Jervell-Lange Nielsen Syndrome
|
|
Prolonged Qt Interval In Ekg And Sudden Death
|
Cardioauditory Syndrome Of Jervell And Lange-Nielsen
|
|
Surdo-Cardiac Syndrome
|
JLNS1
|
|
Deafness, Congenital, And Functional Heart Disease
|
Jlns
|
|
Long Qt Interval-Deafness Syndrome
|
Jervell And Lange-Nielson Syndrome
|
|
Jervell Lange-Nielsen Syndrome
|
Autosomal Recessive Long Qt Syndrome
|
|
Cardio-Auditory-Syncope Syndrome
|
Long Qt Interval-Hearing Loss Syndrome
|
|
Congenital Deafness And Functional Heart Disease
|
Long Qt Interval-Deafness
|
|
|
| Brugada Syndrome 4 |
|
BRGDA4
|
Brugada Syndrome, Type 4
|
|
|
| Intrinsic Cardiomyopathy |
|
|
| Long Qt Syndrome 1 |
|
Romano-Ward Syndrome
|
LQT1
|
|
Ward-Romano Syndrome
|
Rws
|
|
Ventricular Fibrillation With Prolonged Qt Interval
|
Wrs
|
|
Long Qt Syndrome 1, Acquired, Susceptibility To
|
Long Qt Syndrome 1, Acquired
|
|
Romano-Ward Long Qt Syndrome
|
Long Qt Syndrome Type 1
|
|
Long Qt Syndrome-1
|
Acquired Susceptibility To Long Qt Syndrome 1
|
|
Qt Syndrome, Long, Type 1
|
|
|
| Heart Conduction Disease |
|
Conduction Disorder Of The Heart
|
Heart Rhythm Disease
|
|
|
| Sinoatrial Node Disease |
|
Sa Node
|
Sinuatrial Node
|
|
Sinus Node Dysfunction
|
|
|
| Third-Degree Atrioventricular Block |
|
Third Degree Atrioventricular Block
|
Complete Atrioventricular Block
|
|
Complete Av Block
|
Third-Degree Block
|
|
Complete Atrioventricular Heart Block
|
Complete Heart Block
|
|
Third Degree Atrioventricular Heart Block
|
Third Degree Heart Block
|
|
Complete Heart Block Nos
|
Chb - [Complete Heart Block]
|
|
Idioventricular Rhythm
|
Av - [Atrioventricular] Block, Complete
|
|
|
| Scoliosis |
|
|
| First-Degree Atrioventricular Block |
|
First Degree Atrioventricular Block
|
First Degree Heart Block
|
|
Incomplete Atrioventricular Block, First Degree
|
First Degree Atrioventricular Heart Block
|
|
|
| Atrioventricular Block |
|
|
| Bartter Syndrome, Type 4a, Neonatal, With Sensorineural Deafness |
|
Bsnd
|
Sensorineural Deafness With Mild Renal Dysfunction
|
|
Bartter Disease Type 4a
|
BARTS4A
|
|
Bartter Syndrome, Type 4a
|
Bartter Syndrome Type 4
|
|
Bartter Syndrome, Neonatal, With Sensorineural Deafness
|
Bartter Syndrome With Sensorineural Deafness
|
|
Bartter Syndrome Type 4a
|
Neonatal Bartter Syndrome With Sensorineural Deafness
|
|
Bartter Syndrome Type Iv
|
Bartter Syndrome With Sensorineural Hearing Loss
|
|
Bartter Syndrome 4a, Neonatal, With Sensorineural Deafness
|
Hyperprostanglandin E Syndrome 4
|
|
Hypokalemic Alkalosis With Hypercalciuria Antenatal 4
|
Infantile Bartter Syndrome With Sensorineural Deafness
|
|
|
| Brugada Syndrome |
|
Sudden Unexpected Nocturnal Death Syndrome
|
Sudden Unexplained Nocturnal Death Syndrome
|
|
Bangungut
|
Brugada Type Idiopathic Ventricular Fibrillation
|
|
Pokkuri Death Syndrome
|
Sunds
|
|
Idiopathic Ventricular Fibrillation, Brugada Type
|
Sudden Unexplained Death
|
|
Dream Disease
|
Right Bundle Branch Block, St Segment Elevation, And Sudden Death Syndrome
|
|
Sudden Unexplained Death Syndrome
|
Suds
|
|
Sunds - [Sudden Unexplained Nocturnal Death Syndrome]
|
|
|
| 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
|
|
|
| Chromosome 2q35 Duplication Syndrome |
|
Syndactyly
|
Syndactyly Type 1
|
|
Sdty1
|
Zygodactyly
|
|
Syndactyly, Type I
|
Sd1
|
|
Syndactyly, Type 1, With Or Without Craniosynostosis
|
Symphalangism
|
|
Non-Syndromic Syndactyly
|
Symphalangy
|
|
Webbing Of Digits
|
Syndactyly, Type 1
|
|
|
| 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
|
|
|
| Left Ventricular Noncompaction |
|
Noncompaction Cardiomyopathy
|
Left Ventricular Hypertrabeculation
|
|
Lvnc
|
Spongy Myocardium
|
|
Isolated Noncompaction Of The Ventricular Myocardium
|
Left Ventricular Myocardial Noncompaction Cardiomyopathy
|
|
Fetal Myocardium
|
Honeycomb Myocardium
|
|
Hypertrabeculation Syndrome
|
Left Ventricular Non-Compaction
|
|
Lvht
|
Non-Compaction Of The Left Ventricular Myocardium
|
|
Ventricular Noncompaction, Left
|
Non-Compaction Cardiomyopathy
|
|
|
| Autism |
|
Autistic Disorder
|
Autism Susceptibility 1
|
|
Childhood Autism
|
Autistic Disorder Of Childhood Onset
|
|
Infantile Autism
|
Kanner'S Syndrome
|
|
Autistic
|
|
|
| Congenital Myasthenic Syndrome |
|
Congenital Myasthenia
|
Congenital Myasthenic Syndromes
|
|
Cms
|
Myasthenic Syndromes, Congenital
|
|
Myasthenic Syndromes Congenital
|
Myasthenic Syndrome, Congenital
|
|
Congenital Myasthenic Syndrome Ib
|
Congenital And Developmental Myasthenia
|
|
Developmental Myasthenia
|
|
|
| Orofacial Cleft |
|
|
| 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
|
|
|
| Patent Foramen Ovale |
|
Atrial Septal Defect Within Oval Fossa
|
Foramen Ovale Patent
|
|
Ostium Secundum Atrial Septal Defect
|
Atrial Septal Defect, Ostium Secundum Type
|
|
Foramen Ovale, Patent
|
Defect, Patent Or Persistent, Ostium Secundum
|
|
Ostium Secundum Type Atrial Septal Defect
|
Persistent Ostium Secundum
|
|
Asd Ostium Secundum Type
|
Ostium Secundum Asd
|
|
Osasd
|
Asd, Ostium Secundum Type
|
|
Pfo - [Patent Foramen Ovale]
|
Open Foramen Ovale
|
|
Open Oval Foramen
|
Persistent Foramen Ovale
|
|
Secundum Atrial Septal Defect
|
|
|
| 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
|
|
|
| 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
|
|
|
