| Diseases |
Alias |
|
| Sick Sinus Syndrome 1 |
|
SSS1
|
Sinus Node Disease, Familial, Autosomal Recessive
|
|
Sick Sinus Syndrome, Congenital
|
Sinus Bradycardia Syndrome, Familial
|
|
Sinus Rhythm, Congenital Absence Of
|
Autosomal Recessive Sick Sinus Syndrome 1
|
|
Congenital Absence Of Sinus Rhythm
|
Familial Sinus Bradycardia Syndrome
|
|
Familial Sinus Node Disease Autosomal Recessive
|
Sick Sinus Syndrome 1, Autosomal Recessive
|
|
|
| Long Qt Syndrome 3 |
|
LQT3
|
Long Qt Syndrome Type 3
|
|
Long Qt Syndrome-3
|
Qt Syndrome, Long, Type 3
|
|
|
| Timothy Syndrome |
|
Long Qt Syndrome With Syndactyly
|
TS
|
|
Lqt8
|
Long Qt Syndrome 8
|
|
Long Qt Syndrome Type 8
|
Long Qt Syndrome-Syndactyly Syndrome
|
|
|
| Severe Congenital Neutropenia 5 |
|
Congenital Neutropenia-Myelofibrosis-Nephromegaly Syndrome
|
Congenital Neutropenia-Bone Marrow Fibrosis-Nephromegaly Syndrome
|
|
Vps45 Deficiency
|
Scn5
|
|
|
| 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
|
|
|
| Paine Syndrome |
|
Pain Disorder
|
Pain
|
|
Microcephaly With Spastic Diplegia
|
Pain Syndrome
|
|
|
| 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
|
|
|
| Craniometaphyseal Dysplasia, Autosomal Recessive |
|
CMDR
|
Autosomal Recessive Craniometaphyseal Dysplasia
|
|
Craniometaphyseal Dysplasia, Autosomal Recessive Type
|
Dysplasia, Craniometaphyseal, Autosomal Recessive
|
|
|
| Atrial Fibrillation |
|
A-Fib
|
Fibrillation, Atrial
|
|
Af - [Atrial Fibrillation]
|
Rapid Atrial Fibrillation
|
|
A Fib - [Atrial Fibrillation]
|
|
|
| Cardiovascular System Disease |
|
Abnormality Of The Cardiovascular System
|
Disease Of Subdivision Of Hemolymphoid System
|
|
Disorder Of Cardiovascular System
|
Cardiovascular Diseases
|
|
Cardiovascular Disease
|
|
|
| Heart Conduction Disease |
|
Conduction Disorder Of The Heart
|
Heart Rhythm Disease
|
|
|
| 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
|
|
|
| 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
|
|
|
| Developmental And Epileptic Encephalopathy 14 |
|
Malignant Migrating Partial Seizures Of Infancy
|
Eiee14
|
|
Epilepsy Of Infancy With Migrating Focal Seizures
|
Mmpsi
|
|
DEE14
|
Epileptic Encephalopathy, Early Infantile, 14
|
|
Early Infantile Epileptic Encephalopathy 14
|
Malignant Migrating Partial Epilepsy Of Infancy
|
|
Migrating Partial Epilepsy Of Infancy
|
Migrating Partial Seizures Of Infancy
|
|
Mmpei
|
Mpei
|
|
Mpsi
|
Malignant Migrating Focal Seizures Of Infancy
|
|
Migrating Partial Seizures In Infancy
|
Developmental And Epileptic Encephalopathy, 14
|
|
Encephalopathy, Epileptic, Early Infantile, Type 14
|
|
|
| Malignant Hyperthermia |
|
Anesthesia Related Hyperthermia
|
Malignant Hyperpyrexia Due To Anesthesia
|
|
Hyperpyrexia, Malignant
|
Hyperthermia, Malignant
|
|
Malignant Hyperpyrexia
|
Mhs
|
|
Malignant Fever
|
|
|
| Long Qt Syndrome 9 |
|
LQT9
|
Long Qt Syndrome-9
|
|
Qt Syndrome, Long, Type 9
|
|
|
| Cardiomyopathy, Dilated, 1b |
|
Cardiomyopathy, Familial Dilated, 1
|
Cardiomyopathy, Dilated 1b
|
|
CMD1B
|
Cmpd1
|
|
Cardiomyopathy, Familial Dilated
|
Fdc
|
|
Dilated Cardiomyopathy 1b
|
Familial Dilated Cardiomyopathy
|
|
|
| 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
|
|
|
| Monocular Esotropia |
|
|
| Intrinsic Cardiomyopathy |
|
|
| Familial Sick Sinus Syndrome |
|
Familial Sinus Node Dysfunction
|
|
|
| Migraine, Familial Hemiplegic, 3 |
|
FHM3
|
Familial Hemiplegic Migraine 3
|
|
Mhp3
|
Migraine, Hemiplegic, Familial, Type 3
|
|
|
| Contractures, Pterygia, And Spondylocarpotarsal Fusion Syndrome 1a |
|
Multiple Pterygium Syndrome, Autosomal Dominant
|
CPSFS1A
|
|
Contractures, Pterygia, And Spondylocarpostarsal Fusion Syndrome 1a
|
Autosomal Dominant Disease
|
|
Contractures, Pterygia, And Variable Skeletal Fusions Syndrome 1a
|
Cpskf1a
|
|
Pterygium Syndrome, Multiple
|
Autosomal Dominant
|
|
Arthrogryposis, Distal, Type 8, Formerly
|
Da8, Formerly
|
|
Autosomal Dominant Multiple Pterygium Syndrome
|
Distal Arthrogryposis Type 8
|
|
Arthrogryposis, Distal, Type 8
|
Da8
|
|
Pterygium Syndrome, Multiple, Autosomal Dominant
|
Autosomal Dominant Disorder
|
|
|
| Familial Periodic Paralysis |
|
Genetic Periodic Paralysis
|
Paralyses, Familial Periodic
|
|
|
| Atrial Fibrillation, Familial, 10 |
|
ATFB10
|
Fibrillation, Atrial, Familial, Type 10
|
|
|
| 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
|
|
|
| Severe Congenital Neutropenia |
|
Congenital Neutropenia
|
Neutropenia, Severe Congenital
|
|
Congenital Agranulocytosis
|
Infantile Genetic Agranulocytosis
|
|
Kostmann Disease
|
Kostmann'S Agranulocytosis
|
|
Kostmann'S Syndrome
|
Severe Infantile Genetic Neutropenia
|
|
|
| Sinoatrial Node Disease |
|
Sa Node
|
Sinuatrial Node
|
|
Sinus Node Dysfunction
|
|
|
| Progressive Familial Heart Block, Type Ia |
|
PFHB1A
|
Bundle Branch Block
|
|
Heart Block, Nonprogressive
|
Lenegre-Lev Disease
|
|
Hereditary Bundle Branch System Defect
|
Progressive Familial Heart Block Type Ia
|
|
Pfhbia
|
Pccd
|
|
Hbbd
|
Progressive Familial Heart Block, Type 1a
|
|
Heart Block, Progressive Familial, Type I
|
Pfhbi
|
|
Cardiac Conduction Defect, Progressive
|
Heart Block, Progressive, Type Ia
|
|
Progressive Familial Heart Block Type 1a
|
Familial Progressive Cardiac Conduction Defect
|
|
Heart Block Progressive Familial Type 1
|
Familial Lenègre Disease
|
|
Familial Lev Disease
|
Familial Lev-Lenègre Disease
|
|
Familial Pccd
|
Familial Progressive Heart Block
|
|
Hereditary Bundle Branch Defect
|
Progressive Familial Heart Block
|
|
Progressive Familial Heart Block 1a
|
Cardiac Conduction Defect
|
|
Progressive Cardiac Conduction Defect
|
Progressive Familial Heart Block Type I
|
|
Heart Block, Progressive, Familial, Type 1a
|
Bundle-Branch Block
|
|
Conduction Disorder Of The Heart
|
|
|
| Syncope |
|
|
| Familial Atrial Fibrillation |
|
Atrial Fibrillation, Familial
|
Atfb
|
|
Atrial Fibrillation Autosomal Dominant
|
Autosomal Dominant Atrial Fibrillation
|
|
Auricular Fibrillation
|
Atrial Fibrillation
|
|
Atrial Fibrillation, Familial, 1
|
|
|
| Familial Isolated Dilated Cardiomyopathy |
|
Familial Or Idiopathic Dilated Cardiomyopathy
|
|
|
| Long Qt Syndrome 14 |
|
LQT14
|
Long Qt Syndrome, Type 14
|
|
|
| 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
|
|
|
| Early Infantile Epileptic Encephalopathy |
|
Early Infantile Epileptic Encephalopathy With Suppression Bursts
|
Early Infantile Epileptic Encephalopathy With Burst-Suppression
|
|
Eiee
|
Early Infantile Epileptic Encephalopathy With Suppression-Bursts
|
|
Ohtahara Syndrome
|
Encephalopathy, Epileptic, Early Infantile
|
|
|
| Pontocerebellar Hypoplasia, Type 14 |
|
PCH14
|
Pontocerebellar Hypoplasia Type 14
|
|
Pontocerebellar Hypoplasia 14
|
Doid:0112325
|
|
|
| Wolff-Parkinson-White Syndrome |
|
Wolff-Parkinson-White Pattern
|
Wpw Syndrome
|
|
Anomalous Atrioventricular Excitation
|
Anomalous A-V Excitation
|
|
Ventricular Pre-Excitation With Arrhythmia
|
WPWS
|
|
Ventricular Familial Preexcitation Syndrome
|
Preexcitation Syndrome
|
|
Ventricular Preexcitation
|
Wpw - [Wolff-Parkinson- White] Syndrome
|
|
Pre-Excitation Syndrome
|
|
|
| Neuroblastoma |
|
Nb
|
Neuroblastoma, Susceptibility To
|
|
Neuroblastomas
|
Central Neuroblastoma
|
|
|
| Right Bundle Branch Block |
|
Right Bundle Branch Block With Left Posterior Fascicular Block
|
|
|
| Dravet Syndrome |
|
Severe Myoclonic Epilepsy Of Infancy
|
Smei
|
|
Severe Myoclonic Epilepsy In Infancy
|
Epileptic Encephalopathy, Early Infantile, 6
|
|
DRVT
|
Developmental And Epileptic Encephalopathy 6a
|
|
Dee6a
|
Eiee6
|
|
Dee6
|
Developmental And Epileptic Encephalopathy 6
|
|
Early Infantile Epileptic Encephalopathy 6
|
Myoclonic Epilepsy, Severe, Of Infancy
|
|
Sme
|
Severe Myoclonus Epilepsy Of Infancy
|
|
Borderline Smei
|
Smeb
|
|
Smeb-M
|
Smeb-O
|
|
Smeb-Sw
|
Smei-Borderland
|
|
Smei-Borderland More Than One Feature
|
Smei-Borderland-Myoclonic Seizures
|
|
Smei-Borderland-Spike Wave
|
Intractable Childhood Epilepsy With Generalized Tonic-Clonic Seizures
|
|
ICEGTC
|
Developmental And Epileptic Encephalopathy, 6
|
|
Infantile Severe Myoclonic Epilepsy
|
Epilepsy, Intractable Childhood, With Generalized Tonic-Clonic Seizures
|
|
|
| Hypertrophic Cardiomyopathy |
|
Hypertrophic Obstructive Cardiomyopathy
|
Cardiomyopathy, Hypertrophic
|
|
Cardiomyopathy, Hypertrophic, Familial
|
Familial Hypertrophic Cardiomyopathy
|
|
Cardiomyopathy Hypertrophic Obstructive
|
Idiopathic Myocardial Hypertrophy
|
|
Idiopathic Hypertrophic Cardiomyopathy
|
Obstructive Idiopathic Hypertrophic Cardiomyopathy
|
|
Obstructive Cardiomyopathy
|
Idiopathic Hypertrophic Subaortic Stenosis
|
|
Muscular Subaortic Stenosis
|
Hypertrophic Obstructive Subaortic Stenosis
|
|
|
| Generalized Epilepsy With Febrile Seizures Plus |
|
Gefs+
|
Genetic Epilepsy With Febrile Seizures Plus
|
|
Generalized Epilepsy With Febrile Seizures-Plus
|
Genetic Epilepsy With Febrile Seizures-Plus
|
|
Epilepsy, Generalized, With Febrile Seizures Plus
|
|
|
| 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
|
|
|
| Ebstein Anomaly |
|
Ebstein'S Anomaly
|
Ebstein'S Anomaly Of Common Atrioventricular Valve
|
|
Ebstein'S Anomaly Of Right Atrioventricular Valve
|
Ebstein'S Anomaly Of Tricuspid Valve
|
|
Ebstein'S Malformation
|
Ebstein Malformation Of The Tricuspid Valve
|
|
Ebstein Anomaly Of The Tricuspid Valve
|
Ebstein Disease
|
|
Accessory Tricuspid Valve Tissue
|
Congenital Ebstein Deformity Of Tricuspid Valve
|
|
Ebstein Syndrome
|
Ebstein Cardiopathy
|
|
Ebstein Anomaly Of Tricuspid Valve
|
|
|
| Developmental And Epileptic Encephalopathy |
|
Encephalopathy, Developmental And Epileptic
|
|
|
| Palmoplantar Keratoderma And Congenital Alopecia 1 |
|
Autosomal Dominant Palmoplantar Keratoderma And Congenital Alopecia
|
PPKCA1
|
|
Keratoderma-Hypotrichosis-Leukonychia Totalis Syndrome
|
Autosomal Dominant Palmoplantar Hyperkeratosis And Congenital Alopecia
|
|
Palmoplantar Keratoderma And Congenital Alopecia, Stevanovic Type
|
Ppk-Ca, Stevanovic Type
|
|
Ppkca, Stevanovic Type
|
Palmoplantar Keratoderma With Congenital Alopecia
|
|
Ppkca Stevanovic Type
|
Alopecia Congenita With Hyperkeratosis Of The Palms And Soles
|
|
Alopecia Congenita Keratosis Palmoplantaris
|
Keratoderma, Palmoplantar, With Congenital Alopecia, Type 1
|
|
|
| Heart Disease |
|
Heart Failure
|
Congenital Heart Disease
|
|
Heart Diseases
|
Congenital Heart Defects
|
|
Congenital Heart Defect
|
Congenital Anomaly Of Heart
|
|
Heart Defect
|
Heart Malformation
|
|
Heart-Congenital Defect
|
Congenital Heart Disorder
|
|
Heart Defects Congenital
|
Heart Defects, Congenital
|
|
Heart Defects
|
Heart Disease, Congenital
|
|
Disease, Heart, Congenital
|
Congestive Heart Failure
|
|
|
| Left Ventricular Noncompaction |
|
Left Ventricular Hypertrabeculation
|
Noncompaction Cardiomyopathy
|
|
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
|
|
|
| Ventricular Fibrillation, Paroxysmal Familial, 1 |
|
Paroxysmal Familial Ventricular Fibrillation
|
Ivf
|
|
Ventricular Fibrillation, Idiopathic
|
VF1
|
|
Vf
|
Ventricular Fibrillation, Familial, 1
|
|
Paroxysmal Ventricular Fibrillation
|
Idiopathic Ventricular Fibrillation
|
|
Ventricular Fibrillation, Paroxysmal Familial, Type 1
|
Ventricular Fibrillation
|
|
Ventricular Fibrillation, Paroxysmal Familial
|
Familial Paroxysmal Ventricular Fibrillation 1
|
|
Susceptibility To Ventricular Fibrillation During Myocardial Infarction
|
Ventricular Fibrillation Adverse Event
|
|
|
| Restrictive Cardiomyopathy |
|
Familial Restrictive Cardiomyopathy
|
Cardiomyopathy, Restrictive
|
|
Cardiomyopathy, Constrictive
|
Primary Restrictive Cardiomyopathy
|
|
Rcm
|
Cardiomyopathy Restrictive
|
|
|
| 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
|
|
|
| Trichothiodystrophy 7, Nonphotosensitive |
|
TTD7
|
Nonphotosensitive Trichothiodystrophy 7
|
|
Trichothiodystrophy 7, Non-Photosensitive
|
|
|
| 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
|
|
|
| Brugada Syndrome 1 |
|
BRGDA1
|
Sudden Unexplained Nocturnal Death Syndrome
|
|
Right Bundle Branch Block, St Segment Elevation, And Sudden Death Syndrome
|
Sunds
|
|
Brugada Syndrome, Type 1
|
Brugada Syndrome
|
|
|
| Distal Arthrogryposis |
|
Arthrogryposis Multiplex Congenita
|
Arthrogryposis
|
|
Congenital Multiple Arthrogryposis
|
Congenital Arthromyodysplasia
|
|
Fibrous Ankylosis Of Multiple Joints
|
Guerin-Stern Syndrome
|
|
Guérin-Stern Syndrome
|
Myodystrophia Fetalis Deformans
|
|
Otto Syndrome
|
Rocher-Sheldon Syndrome
|
|
Rossi Syndrome
|
Amc
|
|
Multiple Congenital Arthrogryposis
|
Arthrogryposis Syndrome
|
|
Arthrogryposis, Distal
|
Distal Arthrogryposis Syndrome
|
|
Freeman-Sheldon Syndrome
|
Arthrogryposis, Distal, Type 2b
|
|
Congenital Multiplex Arthrogryposis
|
Amyoplasia Congenita
|
|
Congenital Amyoplasia
|
Amc - [Arthrogryposis Multiplex Congenita]
|
|
|
| Autosomal Genetic Disease |
|
Autosomal Hereditary Disorder
|
|
|
| Cardiomyopathy, Dilated, 1e |
|
Left Ventricular Noncompaction 9
|
Left Ventricular Noncompaction 5
|
|
Dilated Cardiomyopathy 1e
|
Dilated Cardiomyopathy 1s
|
|
CMD1E
|
Cdcd2
|
|
Cardiomyopathy, Dilated, 1y
|
CMD1Y
|
|
Cardiomyopathy, Dilated, 1s
|
CMD1S
|
|
Dilated Cardiomyopathy 1y
|
Dilated Cardiomyopathy With Conduction Defect 2
|
|
Dilated Cardiomyopathy With Conduction Disorder And Arrhythmia
|
Cardiomyopathy, Dilated, With Conduction Disorder And Arrhythmia
|
|
Cardiomyopathy, Dilated, With Conduction Defect 2
|
Cardiomyopathy Dilated With Conduction Defect Type 2
|
|
Cardiomyopathy, Dilated 1e
|
Cardiomyopathy, Dilated 1s
|
|
Cardiomyopathy, Dilated 1y
|
Left Ventricular Non-Compaction 5
|
|
LVNC5
|
Left Ventricular Non-Compaction 9
|
|
LVNC9
|
Cardiomyopathy, Dilated, Type 1e
|
|
Cardiomyopathy, Dilated, Type 1s
|
Cardiomyopathy, Dilated, Type 1y
|
|
|
| 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
|
|
|
| Left Bundle Branch Hemiblock |
|
Left Bundle Branch Block
|
Left Bundle-Branch Block
|
|
|
| Cardiac Arrest |
|
Cardiopulmonary Arrest
|
Circulatory Arrest
|
|
Heart Arrest
|
|
|
| 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
|
|
|
| Noonan Syndrome With Multiple Lentigines |
|
Leopard Syndrome
|
Multiple Lentigines Syndrome
|
|
Moynahan Syndrome
|
Cardiomyopathic Lentiginosis
|
|
Progressive Cardiomyopathic Lentiginosis
|
Cardio-Cutaneous Syndrome
|
|
Lentiginosis Profusa
|
Capute-Rimoin-Konigsmark-Esterly-Richardson Syndrome
|
|
Generalized Lentiginosis
|
Gorlin Syndrome Ii
|
|
Lentiginosis Profusa Syndrome
|
Lentigines, Electrocardiographic Conduction Abnormalities, Ocular Hypertelorism, Pulmonic Stenosis, Abnormal Genitalia, Retardation Of Growth, Deafnes
|
|
Diffuse Lentiginosis
|
Nsml
|
|
Familial Multiple Lentigines Syndrome
|
Alopecia-Epilepsy-Intellectual Disability Syndrome, Moynahan Type
|
|
Progressive Cardiomyopathic Lentiginosis Syndrome
|
Alopecia Epilepsy Oligophrenia Syndrome Of Moynahan
|
|
|
| Progressive Familial Heart Block |
|
Hereditary Bundle Branch Defect
|
Hereditary Bundle Branch System Defect
|
|
Familial Lenegre Disease
|
Familial Lev Disease
|
|
Familial Lev-Lenegre Disease
|
Familial Pccd
|
|
Familial Progressive Heart Block
|
Pfhb
|
|
Bundle Branch Block
|
Hbbd
|
|
Lenegre Lev Disease
|
Lev Syndrome
|
|
Lev'S Disease
|
Lev-Lenègre Disease
|
|
Pccd
|
Progressive Cardiac Conduction Defect
|
|
Bundle-Branch Block
|
|
|
| Long Qt Syndrome 2 |
|
LQT2
|
Long Qt Syndrome 2, Acquired, Susceptibility To
|
|
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
|
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
|
|
|
| Palmoplantar Keratoderma, Nonepidermolytic |
|
Nonepidermolytic Palmoplantar Keratoderma
|
NEPPK
|
|
Tylosis
|
Unna-Thost Syndrome
|
|
Keratoderma, Palmoplantar, Diffuse
|
Ppkne
|
|
Keratoderma, Nonepidermolytic Palmoplantar
|
Diffuse Nonepidermolytic Palmomplantar Keratoderma
|
|
Thost-Unna Syndrome
|
Non-Epidermolytic Palmoplantar Keratoderma
|
|
Autosomal Dominant Diffuse Palmoplantar Keratoderma, Norrbotten Type
|
Diffuse Palmoplantar Keratoderma, Bothnian Type
|
|
Krt1-Related Diffuse Nonepidermolytic Keratoderma
|
Krt1-Related Diffuse Neppk
|
|
Keratoderma, Palmoplantar, Non-Epidermolytic
|
Nonepidermolytic Unna-Thost Disease
|
|
Non-Epidermolytic Unna-Thost Disease
|
Keratoderma, Palmoplantar, Nonepidermolytic
|
|
Hyperkeratosis
|
|
|
| First-Degree Atrioventricular Block |
|
First Degree Atrioventricular Block
|
First Degree Heart Block
|
|
Incomplete Atrioventricular Block, First Degree
|
First Degree Atrioventricular Heart Block
|
|
|
| Atrial Heart Septal Defect |
|
Atrial Septal Defect
|
Atrial Septal Defects
|
|
Atrioseptal Defect
|
Auricular Septal Defect
|
|
Congenital Atrial Septal Defect
|
Interatrial Septal Defect
|
|
Interauricular Septal Defect
|
Heart Septal Defects, Atrial
|
|
Septal Defect, Atrial
|
|
|
| Cardiomyopathy, Dilated, With Woolly Hair And Keratoderma |
|
Carvajal Syndrome
|
Palmoplantar Keratoderma With Left Ventricular Cardiomyopathy And Woolly Hair
|
|
DCWHK
|
Dilated Cardiomyopathy With Woolly Hair And Keratoderma
|
|
Cardiomyopathy Dilated With Woolly Hair And Keratoderma
|
Kwwh Type Ii
|
|
Keratoderma With Woolly Hair Type Ii
|
Woolly Hair-Palmoplantar Hyperkeratosis-Dilated Cardiomyopathy Syndrome
|
|
Woolly Hair-Palmoplantar Keratoderma-Dilated Cardiomyopathy Syndrome
|
Wooly Hair-Palmoplantar Hyperkeratosis-Dilated Cardiomyopathy Syndrome
|
|
Wooly Hair-Palmoplantar Keratoderma-Dilated Cardiomyopathy Syndrome
|
Epidermolytic Palmoplantar Keratoderma Woolly Hair And Dilated Cardiomyopathy
|
|
Wooly Hair - Palmoplantar Keratoderma - Dilated Cardiomyopathy
|
Cardiomyopathy, Dilated With Woolly Hair And Keratoderma
|
|
|
| Idiopathic Ventricular Fibrillation, Non Brugada Type |
|
Familial Paroxysmal Ventricular Fibrillation, Non Brugada Type
|
|
|
| Mitochondrial Dna Depletion Syndrome 12b |
|
|
| Naxos Disease |
|
Mal De Naxos
|
NXD
|
|
Cardiomyopathy, Arrhythmogenic Right Ventricular, With Skin, Hair, And Nail Abnormalities
|
Woolly Hair, Palmoplantar Keratoderma, And Cardiac Abnormalities
|
|
Palmoplantar Keratoderma With Arrhythmogenic Right Ventricular Cardiomyopathy And Woolly Hair
|
Keratosis Palmoplantaris With Arrythmogenic Cardiomyopathy
|
|
Keratosis Palmoplantaris With Arrhythmogenic Cardiomyopathy
|
Keratosis Palmoplantaris Arrythmogenic Cardiomyopathy Woolly Hair
|
|
Woolly Hair Palmoplantar Keratoderma Cardiac Abnormalities
|
Kwwh Type I
|
|
Keratoderma With Woolly Hair Type I
|
Palmoplantar Hyperkeratosis With Arrythmogenic Cardiomyopathy
|
|
Palmoplantar Keratoderma With Arrythmogenic Cardiomyopathy
|
|
|
| Axonal Neuropathy |
|
|
| 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
|
|
|
| Brugada Syndrome 4 |
|
BRGDA4
|
Brugada Syndrome, Type 4
|
|
|
| Fetal Akinesia Deformation Sequence 1 |
|
Fetal Akinesia Deformation Sequence
|
Fads
|
|
Fetal Akinesia Sequence
|
FADS1
|
|
Arthrogryposis Multiplex Congenita With Pulmonary Hypoplasia
|
Pena-Shokeir Syndrome Type 1
|
|
Fetal Akinesia Deformation Sequence Syndrome
|
Arthrogryposis Multiplex Congenita-Pulmonary Hypoplasia Syndrome
|
|
Arthrogryposis Multiplex Congenita Pulmonary Hypoplasia
|
Pena-Shokeir Syndrome, Type I
|
|
Foetal Akinesia Deformation Sequence Syndrome
|
Foetal Akinesia Sequence
|
|
Fetal Akinesia Deformation Sequence Syndrome 1
|
Pena-Shokeir Syndrome, Type 1
|
|
Pena Shokeir Syndrome, Type 1
|
Akinesia, Fetal, Deformation Sequence
|
|
Akinesia, Fetal, Deformation Sequence, Type 1
|
Pena-Shokeir Syndrome Type I
|
|
|
| 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
|
|
|
| Short Qt Syndrome |
|
Sqts
|
Familial Short Qt Syndrome
|
|
|
| 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
|
|
Hypertrophic Cardiomyopathy
|
Cardiomyopathy, Hypertrophic, 1
|
|
Familial Asymmetric Septal Hypertrophy
|
Heritable Hypertrophic Cardiomyopathy
|
|
Idiopathic Hypertrophic Subaortic Stenosis
|
Fhc
|
|
Cardiomyopathy, Hypertrophic, Familial, Type 1
|
Cardiomyopathy, Hypertrophic, Familial
|
|
|
| Familial Progressive Cardiac Conduction Defect |
|
Familial Lenegre Disease
|
Familial Lev Disease
|
|
Familial Lev-Lenegre Disease
|
Familial Pccd
|
|
Familial Progressive Heart Block
|
Hereditary Bundle Branch Defect
|
|
Hereditary Bundle Branch System Defect
|
|
|
| Long Qt Syndrome 12 |
|
LQT12
|
Qt Syndrome, Long, Type 12
|
|
|
| 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
|
|
|
| Atrial Standstill 1 |
|
ATRST1
|
Atrial Cardiomyopathy With Heart Block
|
|
Cardiomyopathy, Familial, With Conduction Disturbance
|
Atrial Standstill, Digenic
|
|
Familial Cardiomyopathy With Conduction Disturbance
|
Standstill, Atrial, Type 1
|
|
Heart Block
|
Cardiomyopathies
|
|
Idiopathic Cardiomyopathy
|
Idiopathic Cardiopathy
|
|
Primary Myocardial Disease
|
Primary Cardiomyopathy
|
|
Myocardiopathy
|
Myocardosis
|
|
Primary Idiopathic Myocardial Disease
|
|
|
| Lipoprotein Quantitative Trait Locus |
|
Coronary Artery Disease
|
Coronary Artery Disease, Susceptibility To
|
|
Coronary Artery Anomaly
|
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
|
|
|
| Long Qt Syndrome |
|
Romano-Ward Syndrome
|
Long Q-T Syndrome
|
|
Lqt
|
Qt Syndrome, Long
|
|
Congenital Long Qt Syndrome
|
Familial Long Qt Syndrome
|
|
|
| Trigeminal Nerve Disease |
|
Trigeminal Nerve Diseases
|
Disorders Of 5th Cranial Nerve
|
|
Disorders Of The Fifth Cranial Nerve
|
|
|
| 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
|
|
|
| Brugada Syndrome 6 |
|
BRGDA6
|
Brugada Syndrome, Type 6
|
|
|
| Atrial Standstill |
|
Atrial Cardiomyopathy With Heart Block
|
Standstill, Atrial
|
|
Cardiomyopathy, Familial, With Conduction Disturbance
|
|
|
| Second-Degree Atrioventricular Block |
|
Second-Degree Heart Block
|
Second Degree Atrioventricular Block
|
|
Second Degree Atrioventricular Heart Block
|
Second Degree Heart Block
|
|
Incomplete Atrioventricular Block, Second Degree Nos
|
Second-Degree Block, Type 1 And 2
|
|
Atrioventricular Block, Type 1 And 2
|
Second Degree Incomplete Atrioventricular Block
|
|
Av - [Atrioventricular] Block 2nd
|
|
|
| Familial Isolated Arrhythmogenic Right Ventricular Dysplasia |
|
Familial Isolated Arvc
|
Familial Isolated Arvd
|
|
Familial Isolated Arrhythmogenic Right Ventricular Cardiomyopathy
|
Familial Isolated Arrhythmogenic Ventricular Cardiomyopathy
|
|
Familial Isolated Arrhythmogenic Ventricular Dysplasia
|
|
|
| Paroxysmal Extreme Pain Disorder |
|
PEPD
|
Familial Rectal Pain
|
|
Pexpd
|
Submandibular, Ocular, And Rectal Pain With Flushing
|
|
Pain, Submandibular, Ocular, And Rectal, With Flushing
|
Rectal Pain, Familial
|
|
Submandibular, Ocular And Rectal Pain With Flushing
|
Familial Rectal Syndrome
|
|
Frp
|
Pain Disorder, Paroxysmal, Extreme
|
|
|
| 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 10 |
|
LQT10
|
Atrial Fibrillation, Familial, 17
|
|
ATFB17
|
Long Qt Syndrome-10
|
|
Qt Syndrome, Long, Type 10
|
|
|
| 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
|
|
|
| Cardiac Sarcoidosis |
|
|
| Epilepsy, Idiopathic Generalized |
|
Idiopathic Generalized Epilepsy
|
Generalised Epilepsy
|
|
Epilepsy, Generalized
|
EIG
|
|
Ige
|
Epilepsy, Idiopathic Generalized, Susceptibility To, 1
|
|
Epilepsy, Idiopathic Generalized 1
|
Epilepsy, Idiopathic Generalized, Susceptibility To
|
|
Epilepsy, Idiopathic, Generalized
|
Epilepsy, Idiopathic, Generalized, Susceptibility To, Type 1
|
|
|
| Familial Long Qt Syndrome |
|
Congenital Long Qt Syndrome
|
Lqts
|
|
|
| Sudden Infant Death Syndrome |
|
SIDS
|
Sudden Infant Death Syndrome, Susceptibility To
|
|
Cot Death
|
Crib Death
|
|
Sudden Death Of Nonspecific Cause In Infancy
|
Sudden Infant Death
|
|
Death, Sudden, Syndrome, Infant
|
|
|
| Long Qt Syndrome 13 |
|
LQT13
|
Qt Syndrome, Long, Type 13
|
|
|
| Brugada Syndrome 5 |
|
BRGDA5
|
Cardiac Conduction Defect, Nonspecific
|
|
Brugada Syndrome, Type 5
|
|
|
| Erythromelalgia |
|
Primary Erythromelalgia
|
Erythermalgia
|
|
Primary Erythermalgia
|
Mitchell Disease
|
|
Familial Erythromelalgia
|
|
|
| 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
|
|
|
| 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]
|
|
|
| Atrioventricular Block |
|
|
| Rasopathy |
|
Ras/Mitogen-Activated Protein Kinase Syndrome
|
|
|
| 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
|
|
|
| Familial Woolly Hair Syndrome |
|
Wooly Hair
|
Familial Wooly Hair Syndrome
|
|
Hereditary Woolly Hair Syndrome
|
Hereditary Wooly Hair Syndrome
|
|
Woolly Hair
|
Syndrome With Woolly Hair
|
|
Wooly Hair Syndrome
|
|
|
