| 疾病名称 |
别名 |
|
| Timothy Syndrome |
|
Long Qt Syndrome With Syndactyly
|
TS
|
|
Lqt8
|
Long Qt Syndrome 8
|
|
Long Qt Syndrome Type 8
|
Long Qt Syndrome-Syndactyly Syndrome
|
|
|
| Long Qt Syndrome 8 |
|
|
| Brugada Syndrome 3 |
|
BRGDA3
|
Brugada Syndrome, Type 3
|
|
|
| Neurodevelopmental Disorder With Hypotonia, Language Delay, And Skeletal Defects With Or Without Seizures |
|
|
| Cacna1c-Related Disorders |
|
|
| Timothy Syndrome Type 1 |
|
|
| Long Qt Syndrome |
|
Romano-Ward Syndrome
|
Long Q-T Syndrome
|
|
Lqt
|
Qt Syndrome, Long
|
|
Congenital Long Qt Syndrome
|
Familial Long Qt Syndrome
|
|
|
| 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]
|
|
|
| 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
|
|
|
| Ventricular Fibrillation, Paroxysmal Familial, 1 |
|
Paroxysmal Familial Ventricular Fibrillation
|
Ivf
|
|
Ventricular Fibrillation, Idiopathic
|
Ventricular Fibrillation
|
|
VF1
|
Vf
|
|
Ventricular Fibrillation, Familial, 1
|
Paroxysmal Ventricular Fibrillation
|
|
Idiopathic Ventricular Fibrillation
|
Ventricular Fibrillation, Paroxysmal Familial, Type 1
|
|
Ventricular Fibrillation, Paroxysmal Familial
|
Familial Paroxysmal Ventricular Fibrillation 1
|
|
Susceptibility To Ventricular Fibrillation During Myocardial Infarction
|
Ventricular Fibrillation Adverse Event
|
|
|
| Heart Conduction Disease |
|
Conduction Disorder Of The Heart
|
Heart Rhythm Disease
|
|
|
| Schizotypal Personality Disorder |
|
|
| Cardiac Conduction Defect |
|
Sudden Cardiac Death
|
Cardiac Conduction Defect, Susceptibility To
|
|
SCD
|
Cardiac Conduction Abnormality
|
|
Death Sudden Cardiac
|
Cardiac Conduction Disease
|
|
Conduction Disorder Of The Heart
|
|
|
| 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
|
|
|
| Sick Sinus Syndrome |
|
Sinus Node Dysfunction
|
Sinus Node Disease
|
|
Sinus Node Infection
|
Snd
|
|
Sss
|
Snd - [Sinus Node Dysfunction]
|
|
Sinoatrial Node Dysfunction
|
Sss - [Sick Sinus Syndrome]
|
|
Sick Sinus
|
Sick Sinus Tachycardia
|
|
|
| Cerebral Palsy |
|
Infantile Cerebral Palsy
|
Mixed Cerebral Palsy
|
|
Palsy Cerebral
|
Palsy, Cerebral
|
|
Cerebral Palsy, Mixed
|
|
|
| Right Bundle Branch Block |
|
Right Bundle Branch Block With Left Posterior Fascicular Block
|
|
|
| Cardiomyopathy, Familial Hypertrophic, 1 |
|
Asymmetric Septal Hypertrophy
|
Familial Hypertrophic Cardiomyopathy
|
|
Hypertrophic Cardiomyopathy 1
|
CMH1
|
|
Hypertrophic Cardiomyopathy 19
|
CMH
|
|
Ventricular Hypertrophy, Hereditary
|
Ash
|
|
Hypertrophic Subaortic Stenosis, Idiopathic
|
Cardiomyopathy, Familial Hypertrophic
|
|
Cardiomyopathy, Hypertrophic, 1, Digenic
|
Cardiomyopathy, Familial Hypertrophic 1
|
|
Hcm
|
Hereditary Ventricular Hypertrophy
|
|
Idiopathic Hypertrophic Subaortic Stenosis
|
Hypertrophic Cardiomyopathy
|
|
Cardiomyopathy, Hypertrophic, Familial
|
Cardiomyopathy, Hypertrophic, 1
|
|
Familial Asymmetric Septal Hypertrophy
|
Heritable Hypertrophic Cardiomyopathy
|
|
Fhc
|
Cardiomyopathy, Hypertrophic, Familial, Type 1
|
|
|
| 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
|
|
|
| Autism |
|
Autistic Disorder
|
Autism Susceptibility 1
|
|
Childhood Autism
|
Autistic Disorder Of Childhood Onset
|
|
Infantile Autism
|
Kanner'S Syndrome
|
|
Autistic
|
|
|
| Arrhythmogenic Right Ventricular Cardiomyopathy |
|
Arrhythmogenic Right Ventricular Dysplasia
|
Arvc
|
|
Arvd
|
Arrhythmogenic Right Ventricular Dysplasia/Cardiomyopathy
|
|
Arvc Cardiomyopathy
|
Arrhythmogenic Right Ventricular Cardiomyopathy-Dysplasia
|
|
Arvd/C
|
Right Ventricular Dysplasia, Arrhythmogenic
|
|
Ventricular Dysplasia, Right, Arrhythmogenic
|
Cardiomyopathy, Ventricular, Right, Arrhythmogenic
|
|
Dysplasia, Arrhythmogenic Right Ventricular
|
|
|
| Short Qt Syndrome |
|
Sqts
|
Familial Short Qt Syndrome
|
|
|
| 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
|
|
|
| Sinoatrial Node Disease |
|
Sa Node
|
Sinuatrial Node
|
|
Sinus Node Dysfunction
|
|
|
| Personality Disorder |
|
Personality Disorders
|
Character Disorder
|
|
Personality
|
Specific Personality Disorders
|
|
Enduring Personality Change After Psychiatric Illness
|
|
|
| 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
|
|
|
| Long Qt Syndrome 3 |
|
LQT3
|
Long Qt Syndrome Type 3
|
|
Long Qt Syndrome-3
|
Qt Syndrome, Long, Type 3
|
|
|
| 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
|
|
|
| Long Qt Syndrome 9 |
|
LQT9
|
Long Qt Syndrome-9
|
|
Qt Syndrome, Long, Type 9
|
|
|
| Long Qt Syndrome 11 |
|
LQT11
|
Long Qt Syndrome-11
|
|
Qt Syndrome, Long, Type 11
|
|
|
| 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
|
|
|
| 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
|
|
|
| Bipolar Disorder |
|
Bipolar Depression
|
Manic Disorder
|
|
Depression, Bipolar
|
Bipolar Disorder Manic Phase
|
|
Depressive-Manic Psych.
|
Manic Bipolar Affective Disorder
|
|
Manic Bipolar I Disorder
|
Manic Depression
|
|
Manic Depressive Disorder
|
Mixed Bipolar Disorder
|
|
Bipolar Affective Disorder
|
Bipolar Affective Psychosis
|
|
Bipolar Spectrum Disorder
|
Manic Depressive Illness
|
|
Depression Bipolar
|
Bipolar Disorder, Mixed
|
|
Major Affective Disorder
|
Major Affective Disorder 1
|
|
Major Affective Disorder 2
|
|
|
| Long Qt Syndrome 13 |
|
LQT13
|
Qt Syndrome, Long, Type 13
|
|
|
| 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 Periodic Paralysis |
|
Genetic Periodic Paralysis
|
Paralyses, Familial Periodic
|
|
|
| Narcolepsy |
|
Paroxysmal Sleep
|
Gelineau Syndrome
|
|
Narcoleptic Syndrome
|
Narcolepsy-Cataplexy Syndrome
|
|
Cataplexy And Narcolepsy
|
Narcolepsy, Without Cataplexy
|
|
Gelineau'S Syndrome
|
Narcolepsy With Or Without Cataplexy
|
|
Narcolepsy Nos
|
|
|
| Immunodeficiency 10 |
|
Immune Dysfunction With T-Cell Inactivation Due To Calcium Entry Defect 2
|
Combined Immunodeficiency Due To Stim1 Deficiency
|
|
IMD10
|
Stim1 Deficiency
|
|
Cid Due To Stim1 Deficiency
|
Immune Dysfunction, With T-Cell Inactivation Due To Calcium Entry Defect 2
|
|
Immunodeficiency, Type 10
|
|
|
| T Cell And Nk Cell Immunodeficiency |
|
|
| Anhidrosis, Isolated, With Normal Sweat Glands |
|
Isolated Anhidrosis With Normal Sweat Glands
|
Dann-Epstein-Sohar Syndrome
|
|
ANHD
|
Isolated Generalized Anhidrosis With Normal Sweat Glands
|
|
Anhidrosis, Familial Generalized, With Normal Sweat Glands
|
|
|
| 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
|
|
|
| Episodic Ataxia, Type 2 |
|
Episodic Ataxia Type 2
|
EA2
|
|
Apca
|
Capa
|
|
Cerebellopathy, Hereditary Paroxysmal
|
Acetazolamide-Responsive Hereditary Paroxysmal Cerebellar Ataxia
|
|
Cerebellar Ataxia, Paroxysmal, Acetazolamide-Responsive
|
Episodic Ataxia With Nystagmus
|
|
Ataxia, Episodic, With Nystagmus
|
Episodic Ataxia, Nystagmus-Associated
|
|
Ataxia, Familial Paroxysmal
|
Acetazolamide-Responsive Episodic Ataxia Syndrome
|
|
Acetazolamide-Responsive, Hereditary, Paroxysmal, Cerebellar Ataxia
|
Ataxia, Familial, Paroxysmal
|
|
Nystagmus-Associated Episodic Ataxia
|
Familial Paroxysmal Ataxia
|
|
Episodic Ataxia 2
|
Ea-2
|
|
Episodic Ataxia Nystagmus-Associated
|
Hereditary Paroxysmal Cerebellopathy
|
|
Ataxia, Episodic, Type 2
|
|
|
| Atrioventricular Block |
|
|
| Familial Hemiplegic Migraine |
|
Hemiplegic Migraine, Familial
|
Hemiplegic-Ophthalmoplegic Migraine
|
|
Fhm
|
Hemiplegic Migraine Familial
|
|
|
| Intrinsic Cardiomyopathy |
|
|
| Cyclothymic Disorder |
|
Cyclothymia
|
Cycloid Personality
|
|
Cyclothymic Personality
|
Affective Personality Disorder
|
|
Cyclothymic Personality Disorder
|
Cycloid Personality Disorder
|
|
|
| Ventricular Tachycardia, Catecholaminergic Polymorphic, 1, With Or Without Atrial Dysfunction And/Or Dilated Cardiomyopathy |
|
Catecholaminergic Polymorphic Ventricular Tachycardia 1
|
Ventricular Tachycardia, Catecholaminergic Polymorphic, 1
|
|
CPVT1
|
Ventricular Tachycardia, Stress-Induced Polymorphic
|
|
Vtsip
|
Bidirectional Tachycardia
|
|
Stress-Induced Polymorphic Ventricular Tachycardia
|
Cvpt1
|
|
Double Tachycardia Induced By Catecholamines
|
Malignant Paroxysmal Ventricular Tachycardia
|
|
Multifocal Ventricular Premature Beats
|
Paroxysmal Ventricular Fibrillation
|
|
Syncopal Paroxysmal Tachycardia
|
Syncopal Tachyarythmia
|
|
Ventricular Tachycardia Catecholaminergic Polymorphic 1
|
Tachycardia, Ventricular, Catecholaminergic Polymorphic, Type 1
|
|
Multifocal Pvcs
|
Multifocal Premature Ventricular Beats
|
|
Paroxysmal Familial Ventricular Fibrillation
|
Catecholaminergic Polymorphic Ventricular Tachycardia Type 1
|
|
|
| Brugada Syndrome 4 |
|
BRGDA4
|
Brugada Syndrome, Type 4
|
|
|
| Bipolar I Disorder |
|
Manic Depression Nos
|
Manic-Depressive Illness
|
|
Bipolar Disorder Nos
|
|
|
| Spinocerebellar Ataxia 6 |
|
Spinocerebellar Ataxia Type 6
|
SCA6
|
|
Type 6 Spinocerebellar Ataxia
|
Spinocerebellar Ataxia-6
|
|
Ataxia, Spinocerebellar, Type 6
|
|
|
| Fleck Retina, Familial Benign |
|
FRFB
|
Familial Benign Flecked Retina
|
|
Familial Benign Fleck Retina
|
|
|
| Pervasive Developmental Disorder |
|
Pervasive Development Disorder
|
Pervasive Developmental Disorders
|
|
Pervasive Child Development Disorders
|
Autistic Behavior
|
|
Autism Spectrum Disorders
|
|
|
| Inner Ear Disease |
|
Labyrinthine Dysfunction
|
Diseases Of Inner Ear
|
|
Labyrinthine Disease
|
Abnormality Of The Inner Ear
|
|
Labyrinth Diseases
|
Labyrinthine Disorder
|
|
Nonfunctioning Labyrinth
|
Labyrinthine Loss Of Function
|
|
Labyrinthine Syndrome
|
Labyrinthine Disorder Nos
|
|
|
| Mental Depression |
|
Depression
|
Depressive Disorder
|
|
|
| Familial Atrial Fibrillation |
|
Atrial Fibrillation, Familial
|
Atfb
|
|
Atrial Fibrillation Autosomal Dominant
|
Autosomal Dominant Atrial Fibrillation
|
|
Auricular Fibrillation
|
Atrial Fibrillation
|
|
Atrial Fibrillation, Familial, 1
|
|
|
| Episodic Ataxia |
|
Isaacs Syndrome
|
Neuromyotonia
|
|
Isaacs' Syndrome
|
Acquired Neuromyotonia
|
|
Continuous Muscle Fiber Activity Syndrome
|
Quantal Squander Syndrome
|
|
Isaacs-Mertens Syndrome
|
Ea Syndrome
|
|
Episodic Ataxia Syndrome
|
Isaac Syndrome
|
|
Isaac'S-Merten'S Syndrome
|
Isaac-Mertens Syndrome
|
|
Peripheral Nerve Hyperexcitability
|
Ea
|
|
Peripheral Nerve Hyperexcitability Syndrome
|
Ataxia, Episodic
|
|
Isaacs Neuromyotonia
|
Continuous Muscle Fibre Activity
|
|
|
| Synostosis |
|
|
| Schizophrenia |
|
SCZD
|
Schizophrenia With Or Without An Affective Disorder
|
|
Schizophrenia 12
|
Schizophrenia, Susceptibility To
|
|
Schizophrenia-1
|
Dementia Praecox
|
|
Schizophrenia 1
|
|
|
| Malignant Hyperthermia |
|
Anesthesia Related Hyperthermia
|
Malignant Hyperpyrexia Due To Anesthesia
|
|
Hyperpyrexia, Malignant
|
Hyperthermia, Malignant
|
|
Malignant Hyperpyrexia
|
Mhs
|
|
Malignant Fever
|
|
|
| Mood Disorder |
|
Mood Disorders
|
Episodic Mood Disorder
|
|
|
| Psychotic Disorder |
|
Psychotic Disorders
|
Mental Or Behavioural Disorder
|
|
Psychotic
|
Mental Disorders
|
|
|
| Chromosomal Duplication Syndrome |
|
|
| 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
|
|
|
| Congenital Stationary Night Blindness |
|
Night Blindness, Congenital Stationary
|
Congenital Essential Nyctalopia
|
|
Oguchi Disease
|
Blindness, Night, Stationary, Congenital
|
|
|
| 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
|
|
|
| Attention Deficit-Hyperactivity Disorder |
|
Attention Deficit Hyperactivity Disorder
|
ADHD
|
|
Attention Deficit Disorder
|
Attention Deficit-Hyperactivity Disorder, Susceptibility To
|
|
Attention Deficit Disorder With Hyperactivity
|
Hyperkinetic Disorder
|
|
Hyperactivity Of Childhood
|
Attention-Deficit/Hyperactivity Disorder
|
|
Add
|
Addh
|
|
Attention Deficit
|
Attention Deficit Disorder Of Childhood With Hyperactivity
|
|
Attention Deficit Disorder With Hyperactivity Syndrome
|
Hyperkinetic Syndrome
|
|
Attention-Deficit Hyperactivity Disorder
|
Attention-Deficit/Hyperactivity Disorder, Predominantly Inattentive Type
|
|
Disturbance Of Activity And Attention
|
Disorder Of Activity And Attention
|
|
Adhd - [Attention Deficit Hyperactivity Disorder]
|
Hyperkinetic Disorders
|
|
Disorder Of Activity And Attention With Hyperkinesia
|
Attention Deficit Syndrome With Hyperactivity
|
|
|
| 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
|
|
|
| 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
|
|
|
| Isolated Elevated Serum Creatine Phosphokinase Levels |
|
Elevated Serum Cpk
|
Idiopathic Hyperckemia
|
|
Isolated Hyperckemia
|
Elevated Serum Creatine Phosphokinase
|
|
H-Ck
|
Idiopathic Persistent Elevation Of Serum Creatine Kinase
|
|
|
| Inflammatory Bowel Disease |
|
Inflammatory Bowel Diseases
|
Bowel Disease, Inflammatory
|
|
|
| Migraine With Or Without Aura 1 |
|
Migraine
|
Migraine With Or Without Aura, Susceptibility To, 1
|
|
Migraine Disorder
|
Migraine Variant
|
|
Migraines
|
Migraine Disorders
|
|
Mgr1
|
Mgau
|
|
Ma
|
Migraine With Or Without Aura
|
|
Classic Migraine
|
Common Migraine
|
|
Disorder, Migraine
|
Headache Migraine
|
|
Headache Migrainous
|
Migraine Headache
|
|
Migraine Syndrome
|
Headache Including Migraine
|
|
Migraine, Susceptibility To
|
|
|
| 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
|
|
|
| Chromosome 22q11.2 Deletion Syndrome, Distal |
|
22q11.2 Deletion Syndrome
|
Autosomal Dominant Opitz G/Bbb Syndrome
|
|
Catch22
|
Cayler Cardiofacial Syndrome
|
|
Conotruncal Anomaly Face Syndrome
|
Digeorge Syndrome
|
|
Sedlackova Syndrome
|
Shprintzen Syndrome
|
|
Velocardiofacial Syndrome
|
22q11.2 Distal Deletion Syndrome
|
|
Distal 22q11.2 Microdeletion Syndrome
|
22q11.2ds
|
|
Vcfs
|
Velo-Cardio-Facial Syndrome
|
|
Distal Chromosome 22q11.2 Deletion Syndrome
|
Chromosome 22q11.2 Deletion Syndrome Distal
|
|
Chromosome 22q11.2 Deletion Syndrome
|
Deletion 22q11.2 Syndrome
|
|
22q11ds
|
Catch 22
|
|
Digeorge Sequence
|
Microdeletion 22q11.2
|
|
Monosomy 22q11
|
Takao Syndrome
|
|
Distal Del(22)(Q11.2)
|
Distal Monosomy 22q11.2
|
|
Catch 22 Syndrome
|
Chromosome Deletion Syndrome 22q11.2, Distal
|
|
|
| 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
|
|
|
| Rasopathy |
|
Ras/Mitogen-Activated Protein Kinase Syndrome
|
|
|
