| 疾病名称 |
别名 |
|
| Myopathy, Myofibrillar, 9, With Early Respiratory Failure |
|
Hereditary Myopathy With Early Respiratory Failure
|
Hmerf
|
|
Myopathy, Proximal, With Early Respiratory Muscle Involvement
|
Edstrom Myopathy
|
|
Mfm-Titinopathy
|
MFM9
|
|
Mprm
|
Hereditary Inclusion Body Myopathy With Early Respiratory Failure
|
|
Hibm-Erf
|
Myofibrillar Myopathy-Titinopathy
|
|
Myofibrillar Myopathy With Early Respiratory Failure
|
Myopathy, Distal, With Early Respiratory Failure, Autosomal Dominant
|
|
Myofibrillar Myopathy 9
|
Myofibrillar Myopathy 9 With Early Respiratory Failure
|
|
Autosomal Dominant Distal Myopathy With Early Respiratory Failure
|
Proximal Myopathy With Early Respiratory Muscle Involvement
|
|
Hereditary Proximal Myopathy With Early Respiratory Failure
|
Admerf
|
|
Edström Myopathy
|
Hmerf-Erf
|
|
|
| Salih Myopathy |
|
Early-Onset Myopathy With Fatal Cardiomyopathy
|
Myopathy, Early-Onset, With Fatal Cardiomyopathy
|
|
Eomfc
|
SALMY
|
|
Salih Cmd
|
Salih Congenital Muscular Dystrophy
|
|
Titinopathy & Early-Onset Myopathy With Fatal Cardiomyopathy
|
Myopathy, Salih
|
|
|
| Cardiomyopathy, Dilated, 1g |
|
Dilated Cardiomyopathy 1g
|
CMD1G
|
|
Cardiomyopathy, Dilated 1g
|
Cardiomyopathy, Dilated, Type 1g
|
|
|
| Cardiomyopathy, Familial Hypertrophic, 9 |
|
Hypertrophic Cardiomyopathy 9
|
CMH9
|
|
Cardiomyopathy, Familial Hypertrophic 9
|
Cardiomyopathy, Hypertrophic, Familial, Type 9
|
|
|
| Muscular Dystrophy, Limb-Girdle, Autosomal Recessive 10 |
|
Muscular Dystrophy, Limb-Girdle, Type 2j
|
Lgmd2j
|
|
LGMDR10
|
Titin-Related Limb-Girdle Muscular Dystrophy R10
|
|
Autosomal Recessive Limb-Girdle Muscular Dystrophy Type 2j
|
Lgmd Type 2j
|
|
Limb-Girdle Muscular Dystrophy Type 2j
|
Titin-Related Lgmd R10
|
|
Limb-Girdle Muscular Dystrophy 2j
|
Limb-Girdle Muscular Dystrophy, Type 2j
|
|
Dystrophy, Muscular, Limb-Girdle, Type 2j
|
|
|
| Tibial Muscular Dystrophy, Tardive |
|
Udd Myopathy
|
TMD
|
|
Tardive Tibial Muscular Dystrophy
|
Tibial Muscular Dystrophy
|
|
|
| Tibial Muscular Dystrophy |
|
Tmd
|
Udd Myopathy
|
|
Distal Titinopathy
|
Finnish Tibial Muscular Dystrophy
|
|
Tardive Tibial Muscular Dystrophy
|
Udd Type Distal Myopathy
|
|
Udd Distal Myopathy
|
Udd-Markesbery Muscular Dystrophy
|
|
Distal Myopathy, Udd Type
|
Distal Myopathies
|
|
Tibial Muscular Dystrophy, Tardive
|
|
|
| Autosomal Recessive Limb-Girdle Muscular Dystrophy Type 2j |
|
Lgmd2j
|
Muscular Dystrophy, Limb-Girdle, Type 2j
|
|
|
| Multiminicore Disease |
|
Multiminicore Myopathy
|
Mmd
|
|
Minicore Disease
|
Minicore Myopathy
|
|
Multi-Core Congenital Myopathy
|
Multi-Core Disease
|
|
Multi-Minicore Disease
|
Multicore Disease
|
|
Multicore Myopathy
|
Minicore Myopathy With External Ophthalmoplegia
|
|
|
| Childhood-Onset Progressive Contractures-Limb-Girdle Weakness-Muscle Dystrophy Syndrome |
|
|
| Myopathy |
|
Muscular Diseases
|
Myopathies
|
|
|
| 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
|
|
|
| Centronuclear Myopathy |
|
Myopathy, Centronuclear
|
Myotubular Myopathy
|
|
Cnm
|
Myopathy, Myotubular
|
|
Congenital Structural Myopathy
|
|
|
| Cardiomyopathy, Dilated, 1h |
|
Dilated Cardiomyopathy 1h
|
Dilated Cardiomyopathy With Conduction Defect
|
|
CMD1H
|
Cardiomyopathy, Dilated, With Conduction Defect
|
|
|
| Arrhythmogenic Right Ventricular Dysplasia, Familial, 1 |
|
Arrhythmogenic Right Ventricular Dysplasia 1
|
Uhl Anomaly
|
|
Arrhythmogenic Right Ventricular Cardiomyopathy 1
|
Arvc1
|
|
ARVD1
|
Cardiomyopathy Right Ventricular Dilated
|
|
Dysplasia, Arrhythmogenic Right Ventricular, Type 1
|
|
|
| Rigid Spine Muscular Dystrophy 1 |
|
Rigid Spine Syndrome
|
RSMD1
|
|
Rss
|
Mdrs1
|
|
Eichsfeld Type Congenital Muscular Dystrophy
|
Desmin-Related Myopathy With Mallory Bodies
|
|
Classic Multiminicore Myopathy
|
Sepn1-Related Myopathy
|
|
Multicore Myopathy, Severe Classic Form
|
Minicore Myopathy, Severe Classic Form
|
|
Multiminicore Disease, Severe Classic Form
|
Muscular Dystrophy, Rigid Spine, 1
|
|
Classic Mmd
|
Classic Multiminicore Disease
|
|
Congenital Merosin-Positive Muscular Dystrophy With Early Spine Rigidity
|
Desmin-Related Myopathy With Mallory Body-Like Inclusions
|
|
Early-Onset Desmin-Related Myopathy
|
Myopathy, Sepn1-Related
|
|
Muscular Dystrophy, Congenital, Merosin-Positive, With Early Spine Rigidity
|
Muscular Dystrophy, Congenital, Eichsfeld Type
|
|
Severe Classic Form Minicore Myopathy
|
Severe Classic Form Multicore Myopathy
|
|
Severe Classic Form Multiminicore Disease
|
Desmin-Related Myopathies With Mallory Bodies
|
|
Muscular Dystrophy, Congenital, Merosin Positive With Early Spine Rigidity
|
Rigid Spine Muscular Dystrophy-1
|
|
Rigid Spine Congenital Muscular Dystrophy
|
Congenital Muscular Dystrophy Eichsfeld Type
|
|
Congenital Muscular Dystrophy Merosin-Positive With Early Spine Rigidity
|
Minicore Myopathy Severe Classic Form
|
|
Multicore Myopathy Severe Classic Form
|
Multiminicore Disease Severe Classic Form
|
|
Dystrophy, Muscular, Rigid Spine, Type 1
|
|
|
| Cardiomyopathy, Dilated, 1a |
|
Dilated Cardiomyopathy 1a
|
Cdcd1
|
|
CMD1A
|
Cardiomyopathy, Familial Idiopathic
|
|
Familial Dilated Cardiomyopathy With Conduction Defect Due To Lmna Mutation
|
Cardiomyopathy, Dilated, With Conduction Defect 1
|
|
Cardiomyopathy, Idiopathic Dilated
|
Cardiomyopathy, Congestive
|
|
Dilated Cardiomyopathy With Conduction Defect 1
|
Cardiomyopathy Dilated With Conduction Defect Type 1
|
|
Cardiomyopathy, Dilated 1a
|
Cardiomyopathy Dilated With Conduction Defect 1
|
|
Cardiomyopathy, Dilated, Type 1a
|
|
|
| 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
|
|
|
| Neuromuscular Disease |
|
Neuromuscular Diseases
|
Neuromuscular Disorders
|
|
Neuromuscular Disorder
|
|
|
| Myopathy, Centronuclear, 2 |
|
Myopathy, Centronuclear, Autosomal Recessive
|
Autosomal Recessive Centronuclear Myopathy
|
|
CNM2
|
Centronuclear Myopathy 2
|
|
Ar-Cnm
|
Myotubular Myopathy, Autosomal Recessive
|
|
Autosomal Recessive Myotubular Myopathy
|
Centronuclear Myopathy Autosomal Recessive
|
|
Myopathy, Centronuclear, Type 2
|
|
|
| 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
|
|
|
| Cardiomyopathy, Dilated, 1b |
|
Cardiomyopathy, Familial Dilated, 1
|
Cardiomyopathy, Dilated 1b
|
|
CMD1B
|
Cmpd1
|
|
Cardiomyopathy, Familial Dilated
|
Fdc
|
|
Dilated Cardiomyopathy 1b
|
Familial 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
|
|
|
| Familial Isolated Arrhythmogenic Ventricular Dysplasia, Biventricular Form |
|
Familial Isolated Arrhythmogenic Ventricular Cardiomyopathy, Biventricular Form
|
|
|
| Familial Isolated Arrhythmogenic Ventricular Dysplasia, Left Dominant Form |
|
Familial Isolated Arrhythmogenic Ventricular Cardiomyopathy, Left Dominant Form
|
|
|
| Familial Isolated Arrhythmogenic Ventricular Dysplasia, Right Dominant Form |
|
Familial Isolated Arrhythmogenic Ventricular Cardiomyopathy, Classic Form
|
Familial Isolated Arrhythmogenic Ventricular Cardiomyopathy, Right Dominant Form
|
|
Familial Isolated Arrhythmogenic Ventricular Dysplasia, Classic Form
|
|
|
| Familial Isolated Dilated Cardiomyopathy |
|
Familial Or Idiopathic Dilated Cardiomyopathy
|
|
|
| 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
|
|
|
| Batten-Turner Congenital Myopathy |
|
Congenital Myopathy
|
Batten Turner Congenital Myopathy
|
|
Myopathy Congenital
|
Myopathy, Congenital
|
|
Myotonia Congenita
|
Benign Congenital Myopathy
|
|
|
| Myocarditis |
|
Myocardial Inflammation
|
Inflammatory Cardiomyopathy
|
|
|
| Limb-Girdle Muscular Dystrophy |
|
Lgmd
|
Limb Girdle Muscular Dystrophy
|
|
Muscular Dystrophies, Limb-Girdle
|
Erb'S Muscular Dystrophy
|
|
Leyden-Mbius Muscular Dystrophy
|
Limb-Girdle Syndrome
|
|
Myopathic Limb-Girdle Syndrome
|
Limb Girdle
|
|
Muscular Dystrophy Limb-Girdle
|
Dystrophy, Muscular, Limb-Girdle
|
|
Lgmd - [Limb-Girdle Muscular Dystrophy]
|
Limb Girdle Muscle Dystrophy
|
|
Limb-Girdle Myopathy
|
|
|
| Left Ventricular Noncompaction 2 |
|
|
| Minicore Myopathy With External Ophthalmoplegia |
|
Multiminicore Disease With External Ophthalmoplegia
|
Congenital Multicore Myopathy With External Ophthalmoplegia
|
|
Minicore Myopathy
|
Multicore Myopathy With External Ophthalmoplegia
|
|
Multicore Myopathy
|
Multiminicore Myopathy Multicore Myopathy With External Ophthalmoplegia
|
|
MMDO
|
Myopathy, Minicore, External Ophthalmoplegia
|
|
|
| Muscular Dystrophy |
|
Muscular Dystrophies
|
Congenital Md
|
|
Congenital Muscular Dystrophy
|
Cmd
|
|
Mdc
|
Dystrophy, Muscular
|
|
Gower'S Muscular Dystrophy
|
Progressive Musclular Dystrophy
|
|
Pseudohypertrophic Atrophy
|
Pseudohypertrophic Muscle Paralysis
|
|
Pseudohypertrophic Muscular Atrophy
|
Pseudohypertrophic Muscular Dystrophy
|
|
Pseudohypertrophic Paralysis
|
Pseudomuscular Hypertrophy
|
|
|
| Muscular Dystrophy, Congenital, Lmna-Related |
|
Congenital Muscular Dystrophy
|
Congenital Muscular Dystrophy Due To Lmna Mutation
|
|
MDCL
|
L-Cmd
|
|
Lmna-Related Congenital Muscular Dystrophy
|
Muscular Dystrophy, Congenital
|
|
Congenital Muscular Dystrophy Lmna-Related
|
Lmna-Related Cmd
|
|
Cmd
|
Mdc
|
|
Muscular Dystrophy Congenital Lmna-Related
|
Dystrophy, Muscular, Congenital, Lmna-Related
|
|
Dystrophy, Muscular, Congenital
|
Hereditary Muscular Dystrophy
|
|
Congenital Hereditary Muscular Dystrophy
|
Congenital Progressive Muscular Dystrophy
|
|
Hereditary Progressive Muscular Dystrophy
|
|
|
| Myasthenia Gravis |
|
MG
|
Acquired Myasthenia
|
|
Autoimmune Myasthenia Gravis
|
Erb-Goldflam Disease
|
|
Mg - [Myasthenia Gravis]
|
Myasthenia Gravis Nos
|
|
Myasthenia
|
|
|
| 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
|
|
|
| Thymoma |
|
Primary Thymic Epithelial Neoplasm
|
Primary Thymic Epithelial Tumor
|
|
Thymus Neoplasms
|
|
|
| Restrictive Cardiomyopathy |
|
Familial Restrictive Cardiomyopathy
|
Cardiomyopathy, Restrictive
|
|
Cardiomyopathy, Constrictive
|
Primary Restrictive Cardiomyopathy
|
|
Rcm
|
Cardiomyopathy Restrictive
|
|
|
| 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
|
|
|
| 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
|
|
|
| Respiratory Failure |
|
Acute Respiratory Failure
|
Chronic Respiratory Failure
|
|
Respiratory Insufficiency
|
Acute-On-Chronic Respiratory Failure
|
|
Respiratory Disease
|
Acute And Chronic Respiratory Failure
|
|
Respiratory Insufficiency/Failure
|
Chronic Respiratory Disease
|
|
Pulmonary Valve Insufficiency
|
Chronic Disease Of Respiratory System
|
|
Respiration Disorders
|
Respiratory Tract Diseases
|
|
Lung Failure Nos
|
Pulmonary Failure
|
|
Arf - [Acute Respiratory Failure]
|
Acute Respiratory Insufficiency
|
|
Acute Pulmonary Insufficiency
|
Acute Respiration Failure
|
|
Chronic Respiration Failure
|
|
|
| Miyoshi Muscular Dystrophy |
|
Distal Myopathy
|
Distal Muscular Dystrophy
|
|
Miyoshi Myopathy
|
Distal Myopathies
|
|
Dystrophy, Muscular, Miyoshi
|
Myopathy, Distal
|
|
Distal Muscular Dystrophies
|
|
|
| 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
|
|
|
| Scoliosis |
|
|
| Cerebral Palsy |
|
Infantile Cerebral Palsy
|
Mixed Cerebral Palsy
|
|
Palsy Cerebral
|
Palsy, Cerebral
|
|
Cerebral Palsy, Mixed
|
|
|
| Familial Atrial Fibrillation |
|
Atrial Fibrillation, Familial
|
Atfb
|
|
Atrial Fibrillation Autosomal Dominant
|
Autosomal Dominant Atrial Fibrillation
|
|
Auricular Fibrillation
|
Atrial Fibrillation
|
|
Atrial Fibrillation, Familial, 1
|
|
|
| Cortical Thymoma |
|
Polygonal Cell Thymoma
|
Thymoma, Cortical
|
|
Thymoma, Type B2
|
|
|
| Lambert-Eaton Myasthenic Syndrome |
|
Lambert-Eaton Syndrome
|
Eaton-Lambert Syndrome
|
|
Lems
|
Lambert Eaton Myasthenic Syndrome
|
|
Eaton Lambert Syndrome
|
Lambert Eaton Syndrome
|
|
Myasthenic Syndrome Of Lambert-Eaton
|
Myasthenic-Myopathic Syndrome Of Lambert-Eaton
|
|
Lems - [Lambert-Eaton Myasthenic Syndrome]
|
|
|
| Myositis |
|
Idiopathic Inflammatory Myopathy
|
Idiopathic Inflammatory Myositis
|
|
Iim
|
Imm
|
|
Idiopathic Inflammatory Myopathies
|
Myopathy, Familial Idiopathic Inflammatory
|
|
Inflammatory Disorder Of Muscle
|
Idiopathic Inflammatory Myopathy, Familial
|
|
Inflammatory Myopathy, Idiopathic
|
Myopathies Idiopathic Inflammatory
|
|
Familial Idiopathic Inflammatory Myopathy
|
|
|
| Foot Drop |
|
|
| Muscular Dystrophy-Dystroglycanopathy , Type C, 5 |
|
Lgmd2i
|
Autosomal Recessive Limb-Girdle Muscular Dystrophy Type 2i
|
|
MDDGC5
|
Limb-Girdle Muscular Dystrophy Due To Fkrp Deficiency
|
|
Limb-Girdle Muscular Dystrophy Type 2i
|
Muscular Dystrophy, Limb-Girdle, Autosomal Recessive 9
|
|
Lgmdr9
|
Muscular Dystrophy, Limb-Girdle, Type 2i
|
|
Muscular Dystrophy-Dystroglycanopathy Limb-Girdle Frkp-Related
|
Fkrp-Related Limb-Girdle Muscular Dystrophy R9
|
|
Fkrp-Related Lgmd R9
|
Lgmd Due To Fkrp Deficiency
|
|
Lgmd Type 2i
|
Muscular Dystrophy-Dystroglycanopathy, Limb-Girdle, Frkp-Related
|
|
Muscular Dystrophy Limb-Girdle Type 2i
|
Muscular Dystrophy-Dystroglycanopathy Type C 5
|
|
Muscular Dystrophy-Dystroglycanopathy Limb-Girdle C5
|
Dystrophy, Muscular, Limb-Girdle, Type 2i
|
|
|
| Cardioneuromyopathy With Hyaline Masses And Nemaline Rods |
|
|
| 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
|
|
|
| Muscular Dystrophy, Limb-Girdle, Autosomal Recessive 2 |
|
Lgmd2b
|
Muscular Dystrophy, Limb-Girdle, Type 2b
|
|
Autosomal Recessive Limb-Girdle Muscular Dystrophy Type 2e
|
Beta-Sarcoglycanopathy
|
|
Autosomal Recessive Limb-Girdle Muscular Dystrophy Type 2y
|
Muscular Dystrophy, Limb-Girdle, Type 3
|
|
Lgmd3
|
Autosomal Recessive Limb-Girdle Muscular Dystrophy Type 2s
|
|
LGMDR2
|
Muscular Dystrophy, Limb-Girdle, Type 2s
|
|
Limb-Girdle Muscular Dystrophy Type 2b
|
Lgmd2e
|
|
Limb-Girdle Muscular Dystrophy Due To Beta-Sarcoglycan Deficiency
|
Muscular Dystrophy, Limb-Girdle, Type 2e
|
|
Lgmd2s
|
Autosomal Recessive Muscular Dystrophy Due To Lap1b Deficiency
|
|
Autosomal Recessive Muscular Dystrophy Due To Torsin-1a-Interacting Protein 1 Deficiency
|
Lgmd2y
|
|
Muscular Dystrophy With Progressive Weakness, Distal Contractures And Rigid Spine
|
Muscular Dystrophy, Limb-Girdle, Type 2y
|
|
Dysferlin-Related Limb-Girdle Muscular Dystrophy R2
|
Autosomal Recessive Limb-Girdle Muscular Dystrophy Type 2b
|
|
Dysferlin-Related Lgmd R2
|
Lgmd Due To Dysferlin Deficiency
|
|
Lgmd Type 2b
|
Limb-Girdle Muscular Dystrophy Due To Dysferlin Deficiency
|
|
Limb-Girdle Muscular Dystrophy 2b
|
Limb-Girdle Muscular Dystrophy, Type 2b
|
|
Dystrophy, Muscular, Limb-Girdle, Autosomal Recessive, Type 2
|
Dystrophy, Muscular, Limb-Girdle, Type 2b
|
|
Limb-Girdle Muscular Dystrophy, Type 2e
|
|
|
| Diastolic Heart Failure |
|
|
| 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
|
|
|
| Muscle Hypertrophy |
|
MSLHP
|
Hypertrophy
|
|
Hypertrophy, Muscle
|
|
|
| Muscular Dystrophy, Limb-Girdle, Autosomal Recessive 7 |
|
Muscular Dystrophy, Limb-Girdle, Type 2g
|
Lgmd2g
|
|
LGMDR7
|
Limb-Girdle Muscular Dystrophy, Type 2g
|
|
Telethonin-Related Limb-Girdle Muscular Dystrophy R7
|
Autosomal Recessive Limb-Girdle Muscular Dystrophy Type 2g
|
|
Lgmd Due To Telethonin Deficiency
|
Lgmd Type 2g
|
|
Limb-Girdle Muscular Dystrophy Due To Telethonin Deficiency
|
Limb-Girdle Muscular Dystrophy Type 2g
|
|
Telethonin-Related Lgmd R7
|
Limb-Girdle Muscular Dystrophy 2g
|
|
Dystrophy, Muscular, Limb-Girdle, Type 2g
|
|
|
| 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
|
|
|
| Rhabdomyosarcoma |
|
|
| Uterine Corpus Endometrial Carcinoma |
|
|
| Dendritic Cell Thymoma |
|
Epithelioid Thymoma
|
Type B Thymoma
|
|
|
| Muscular Dystrophy, Limb-Girdle, Autosomal Recessive 8 |
|
Sarcotubular Myopathy
|
Lgmd2h
|
|
Muscular Dystrophy, Limb-Girdle, Type 2h
|
Limb-Girdle Muscular Dystrophy Type 2h
|
|
LGMDR8
|
Muscular Dystrophy Hutterite Type
|
|
Muscular Dystrophy, Hutterite Type
|
Muscular Dystrophy Limb-Girdle Type 2h
|
|
Trim32-Related Limb-Girdle Muscular Dystrophy R8
|
Autosomal Recessive Limb-Girdle Muscular Dystrophy Type 2h
|
|
Lgmd Due To Trim32 Deficiency
|
Lgmd Type 2h
|
|
Limb-Girdle Muscular Dystrophy Due To Trim32 Deficiency
|
Trim32-Related Lgmd R8
|
|
Limb-Girdle Muscular Dystrophy 2h
|
Dystrophy, Muscular, Limb-Girdle, Type 2h
|
|
|
| Muscular Dystrophy, Limb-Girdle, Autosomal Recessive 4 |
|
Lgmd2e
|
Muscular Dystrophy, Limb-Girdle, Type 2e
|
|
LGMDR4
|
Beta-Sarcoglycan-Related Limb-Girdle Muscular Dystrophy R4
|
|
Autosomal Recessive Limb-Girdle Muscular Dystrophy Type 2e
|
Beta-Sarcoglycan-Related Lgmd R4
|
|
Beta-Sarcoglycanopathy
|
Lgmd Due To Beta-Sarcoglycan Deficiency
|
|
Lgmd Type 2e
|
Limb-Girdle Muscular Dystrophy Due To Beta-Sarcoglycan Deficiency
|
|
Limb-Girdle Muscular Dystrophy Type 2e
|
Limb-Girdle Muscular Dystrophy 2e
|
|
|
| Pulmonary Interstitial Emphysema |
|
|
| Limb-Girdle Muscular Dystrophy Type 1a |
|
Lgmd1a
|
Lgmd1
|
|
Muscular Dystrophy, Proximal, Type 1a
|
Limb-Girdle Muscular Dystrophy, Type 1a
|
|
Dystrophy, Muscular, Limb-Girdle, Type 1a
|
|
|
| Peripartum Cardiomyopathy |
|
Postpartum Cardiomyopathy
|
Peripartum Cardiomyopathy, Susceptibility To
|
|
Ppcm
|
Ppcm, Susceptibility To
|
|
Antepartum Peripartum Cardiomyopathy
|
Postpartum Peripartum Cardiomyopathy
|
|
Meadows' Syndrome
|
Cardiomyopathy, Peripartum
|
|
|
| Muscular Dystrophy, Limb-Girdle, Autosomal Recessive 6 |
|
Lgmd2f
|
Muscular Dystrophy, Limb-Girdle, Type 2f
|
|
Limb-Girdle Muscular Dystrophy Type 2f
|
LGMDR6
|
|
Muscular Dystrophy Limb-Girdle With Delta-Sarcoglyan Deficiency
|
Delta-Sarcoglycan-Related Limb-Girdle Muscular Dystrophy R6
|
|
Autosomal Recessive Limb-Girdle Muscular Dystrophy Type 2f
|
Delta-Sarcoglycan-Related Lgmd R6
|
|
Delta-Sarcoglycanopathy
|
Lgmd Due To Delta-Sarcoglycan Deficiency
|
|
Lgmd Type 2f
|
Limb-Girdle Muscular Dystrophy Due To Delta-Sarcoglycan Deficiency
|
|
Limb-Girdle Muscular Dystrophy 2f
|
Limb-Girdle Muscular Dystrophy, Type 2f
|
|
Dystrophy, Muscular, Limb-Girdle, Type 2f
|
|
|
| Alcoholic Cardiomyopathy |
|
Cardiomyopathy, Alcoholic
|
Alcohol-Induced Heart Muscle Disease
|
|
Dilated Cardiomyopathy Secondary To Alcohol
|
|
|
| Autosomal Recessive Limb-Girdle Muscular Dystrophy Type 2g |
|
Lgmd2g
|
Limb-Girdle Muscular Dystrophy Due To Telethonin Deficiency
|
|
Muscular Dystrophy, Limb-Girdle, Type 2g
|
|
|
| Thymus Gland Disease |
|
|
| 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]
|
|
|
| Autosomal Recessive Limb-Girdle Muscular Dystrophy Type 2a |
|
Leyden-Moebius Muscular Dystrophy
|
Lgmd2a
|
|
Limb-Girdle Muscular Dystrophy Due To Calpain Deficiency
|
Muscular Dystrophy, Limb-Girdle, Type 2a
|
|
Pelvofemoral Muscular Dystrophy
|
Primary Calpainopathy
|
|
|
| Myopathy, Centronuclear, 1 |
|
Autosomal Dominant Centronuclear Myopathy
|
CNM1
|
|
Centronuclear Myopathy 1
|
Ad-Cnm
|
|
Myopathy, Centronuclear, Autosomal Dominant
|
Myotubular Myopathy, Autosomal Dominant
|
|
Centronuclear Myopathy, Autosomal, Modifier Of
|
Autosomal Dominant Myotubular Myopathy
|
|
Dnm2-Related Centronuclear Myopathy
|
Centronuclear Myopathy Autosomal Dominant
|
|
Myopathies, Structural, Congenital
|
Myopathy, Centronuclear, Type 1
|
|
|
| Intrinsic Cardiomyopathy |
|
|
| Axonal Neuropathy |
|
|
| Cardiomyopathy, Dilated, 1dd |
|
Dilated Cardiomyopathy 1dd
|
CMD1DD
|
|
Cardiomyopathy, Dilated 1dd
|
Cardiomyopathy, Dilated, Type 1dd
|
|
|
| Thymus Cancer |
|
Thymic Neoplasm
|
Thymic Tumor
|
|
Thymus Neoplasm
|
Thymus Neoplasms
|
|
Malignant Neoplasm Of Thymus
|
Neoplasm Of Thymus
|
|
Thymic Neoplasms
|
Thymoma, Familial
|
|
Thymic Carcinoma
|
Thymoma, Type C
|
|
Cancer Of Thymus
|
Malignant Tumour Of Thymus
|
|
Primary Malignant Neoplasm Of Thymus
|
Thymic Glandular Cancer
|
|
Thymus Gland Cancer
|
|
|
| Systolic Heart Failure |
|
|
| Myopathy, Distal, 1 |
|
Laing Distal Myopathy
|
Laing Early-Onset Distal Myopathy
|
|
MPD1
|
Distal Myopathy 1
|
|
Myopathy, Distal, Early-Onset, Autosomal Dominant
|
Distal Myopathy Type 1
|
|
Gowers Disease
|
Myopathy, Late Distal Hereditary
|
|
Myopathy Distal, Type 1
|
Myopathy Distal Early-Onset Autosomal Dominant
|
|
Myopathy Late Distal Hereditary
|
Myopathy, Distal, Type 1
|
|
Welander Distal Myopathy
|
|
|
| Muscular Atrophy |
|
Muscle Wasting
|
Amyotrophia
|
|
Wasting - Muscle
|
Skeletal Muscle Atrophy
|
|
|
| Epithelial Malignant Thymoma |
|
Squamoid Thymoma
|
Thymoma, Epithelial
|
|
Well Differentiated Thymic Carcinoma
|
Thymoma, Type B3
|
|
|
| Bilateral Hypoactive Labyrinth |
|
Hypoactive Bilateral Labyrinthine Dysfunction
|
Hypoactive Labyrinth, Bilateral
|
|
|
| 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
|
|
|
| Myopathy, Myofibrillar, 1 |
|
Desmin-Related Myofibrillar Myopathy
|
Desmin-Related Myopathy
|
|
MFM1
|
Myopathy, Myofibrillar, Desmin-Related
|
|
Drm
|
Myofibrillar Myopathy With Arrhythmogenic Right Ventricular Cardiomyopathy
|
|
Desmin-Related Myopathy With Arrhythmogenic Right Ventricular Cardiomyopathy
|
Myofibrillar Myopathy 1
|
|
Desminopathy
|
Muscular Dystrophy, Limb-Girdle, Type 2r
|
|
Arrhythmogenic Right Ventricular Dysplasia, Familial, 7
|
Desminopathy, Primary
|
|
Arrhythmogenic Right Ventricular Dysplasia, Familial, 7, Formerly
|
Arvd7, Formerly
|
|
Arrhythmogenic Right Ventricular Cardiomyopathy 7, Formerly
|
Arvc7, Formerly
|
|
Inclusion Body Myopathy 1, Autosomal Dominant, Formerly
|
Ibm1, Formerly
|
|
Cardiomyopathy, Dilated, 1f And Limb-Girdle Muscular Dystrophy Type 1d, Formerly
|
Cmd1f And Lgmd1d, Formerly
|
|
Cardiomyopathy, Dilated, With Conduction Defect And Muscular Dystrophy
|
Cdcd3, Formerly
|
|
Muscular Dystrophy, Limb-Girdle, Type 2r, Formerly
|
Lgmd2r, Formerly
|
|
Autosomal Recessive Limb-Girdle Muscular Dystrophy Type 2r
|
Arrhythmogenic Right Ventricular Cardiomyopathy 7
|
|
Arvc7
|
Arvd7
|
|
Autosomal Dominant Inclusion Body Myopathy 1
|
Cdcd3
|
|
Cmd1f And Lgmd1d
|
Desminopathy Primary
|
|
Dilated Cardiomyopathy 1f And Limb-Girdle Muscular Dystrophy Type 1d
|
Dilated Cardiomyopathy With Conduction Defect And Muscular Dystrophy
|
|
Familial Arrhythmogenic Right Ventricular Dysplasia 7
|
Lgmd2r
|
|
Limb-Girdle Muscular Dystrophy 2r
|
Mfm Desmin-Related
|
|
Myopathy Myofibrillar Desmin-Related
|
Dystrophy, Muscular, Limb-Girdle, Type 2r
|
|
|
| First-Degree Atrioventricular Block |
|
First Degree Atrioventricular Block
|
First Degree Heart Block
|
|
Incomplete Atrioventricular Block, First Degree
|
First Degree Atrioventricular Heart Block
|
|
|
| Meconium Aspiration Syndrome |
|
Neonatal Aspiration Of Meconium
|
Meconium Aspiration
|
|
Mas
|
Meconium Aspiration Syndrome Of Newborn
|
|
Meconium Inhalation
|
Mas - [Meconium Aspiration Syndrome]
|
|
Meconium Aspiration Nos
|
Meconium Aspiration Syndrome Nos
|
|
Meconium Pneumonitis
|
Meconium Stained Liqueur Aspiration
|
|
|
| Hyaline Body Myopathy |
|
Myosin Storage Myopathy
|
Autosomal Dominant Hyaline Body Myopathy
|
|
Myopathy, Myosin Storage
|
|
|
| Myofibrillar Myopathy |
|
Desmin Related Myopathy
|
Myotilinopathy
|
|
Myopathy, Myofibrillar
|
Alpha Beta Crystallinopathy
|
|
Desmin Storage Myopathy
|
Desminopathy
|
|
Filaminopathy
|
Protein Surplus Myopathy
|
|
Zaspopathy
|
Myofibrillar Myopathies
|
|
Myopathy, Myofibrillar, Desmin-Related
|
Myopathy, Desmin Storage
|
|
Mfm - [Myofibrillar Myopathy]
|
|
|
| Constrictive Pericarditis |
|
Pericarditis, Constrictive
|
Pericarditis Constrictive
|
|
Pericarditis Calculosa
|
Hutinel-Pick Syndrome
|
|
Chronic Tamponade
|
Chronic Pericardial Constriction
|
|
Pick Syndrome Of Heart
|
Pick Disease Of Heart
|
|
Concretio Cordis
|
Calcareous Pericarditis
|
|
|
| Ehlers-Danlos Syndrome |
|
Eds
|
Cutis Hyperelastica
|
|
Elastic Skin
|
Ehlers-Danlos Syndromes
|
|
Ed Syndrome
|
Ehlers Danlos Syndrome
|
|
Ehlers Danlos Disease
|
Eds - [Ehlers-Danlos Syndrome]
|
|
|
| Cardiomyopathy, Familial Hypertrophic, 4 |
|
Hypertrophic Cardiomyopathy 4
|
CMH4
|
|
Cardiomyopathy, Hypertrophic, 4
|
Cardiomyopathy, Familial Hypertrophic 4
|
|
Cardiomyopathy, Familial Hypertrophic, 4, Susceptibility To
|
Cardiomyopathy, Hypertrophic, Familial, Type 4
|
|
|
| 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
|
|
|
| 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]
|
|
|
| Myopathy, Myofibrillar, 3 |
|
Myotilinopathy
|
Myofibrillar Myopathy 3
|
|
MFM3
|
Autosomal Dominant Limb-Girdle Muscular Dystrophy Type 1a
|
|
Lgmd1a
|
Muscular Dystrophy, Limb-Girdle, Type 1a
|
|
Myopathy, Myofibrillar, Myotilin-Related
|
Muscular Dystrophy, Limb-Girdle, Type 1, Formerly
|
|
Lgmd1, Formerly
|
Muscular Dystrophy, Limb-Girdle, Type 1a, Formerly
|
|
Lgmd1a, Formerly
|
Qualitative Or Quantitative Defects Of Myotilin
|
|
Limb-Girdle Muscular Dystrophy Due To Myotilin Deficiency
|
Distal Myotilinopathy
|
|
Lgmd1
|
Limb-Girdle Muscular Dystrophy 1a
|
|
Mfm Myotilin-Related
|
Muscular Dystrophy, Limb-Girdle, Type 1
|
|
Myopathy Myofibrillar Myotylin-Related
|
Myopathy, Myofibrillar, Type 3
|
|
|
| Newborn Respiratory Distress Syndrome |
|
Hyaline Membrane Disease
|
Respiratory Distress Syndrome Of Newborn
|
|
Neonatal Respiratory Distress
|
Hmd - Hyaline Membrane Disease
|
|
Neonatal Respiratory Distress Syndrome
|
Pulmonary Hyaline Membrane Disease
|
|
Pulmonary Hypoperfusion Syndrome Of Newborn
|
Respiratory Distress Syndrome, Newborn
|
|
Respiratory Distress Syndrome
|
Cardiorespiratory Distress Syndrome Of Newborn
|
|
Distress Respiratory Syndrome Newborn
|
Idiopathic Respiratory Distress Syndrome
|
|
Idiopathic Respiratory Distress Syndrome Of Newborn
|
Newborn Idiopathic Respiratory Distress Syndrome
|
|
Respiratory Distress Syndrome In Newborn
|
Rds - [Respiratory Distress Syndrome] Of Newborn
|
|
Newborn Cardiorespiratory Distress Syndrome
|
|
|
| Left Bundle Branch Hemiblock |
|
Left Bundle Branch Block
|
Left Bundle-Branch Block
|
|
|
| Autosomal Recessive Limb-Girdle Muscular Dystrophy |
|
Muscular Dystrophy, Limb-Girdle, Autosomal Recessive
|
|
|
| Myopathy, Myofibrillar, 2 |
|
Alpha-B Crystallinopathy
|
Myofibrillar Myopathy 2
|
|
MFM2
|
Myopathy, Myofibrillar, Alpha-B Crystallin-Related
|
|
Myopathy, Desmin-Related, Associated With Mutation In The Cryab Gene
|
Myopathy, Myofibrillar, With Or Without Cataract And/Or Cardiomyopathy
|
|
Alpha-B Crystallin-Related Late-Onset Myopathy
|
Alpha-B Crystallin-Related Late-Onset Distal Myopathy
|
|
Late-Onset Distal Crystallinopathy
|
Alpha-B Crystallinopathy With Cataract
|
|
Desmin-Related Myopathy With Cataract
|
Mfm Alpha-B Crystallin-Related
|
|
Myofibrillar Myopathy Alpha-B Crystallin-Related
|
Myofibrillar Myopathy With Or Without Cataract And/Or Cardiomyopathy
|
|
Myopathy Cardioskeletal Desmin-Related With Cataract
|
Myopathy Desmin-Related Associated With Mutation In The Cryab Gene
|
|
Myopathy, Cardioskeletal, Desmin-Related, With Cataract
|
Myopathy, Myofibrillar, Type 2
|
|
|
| Hypertensive Heart Disease |
|
|
| Congenital Structural Myopathy |
|
|
| Myopathy, Myofibrillar, 4 |
|
Myofibrillar Myopathy 4
|
MFM4
|
|
Zaspopathy
|
Myopathy, Myofibrillar, Zasp-Related
|
|
|
| Myopathy, Myofibrillar, 5 |
|
Myofibrillar Myopathy 5
|
MFM5
|
|
Myopathy, Myofibrillar, Filamin C-Related
|
Filaminopathy, Autosomal Dominant
|
|
Filaminopathy
|
Muscle Filaminopathy
|
|
Autosomal Dominant Filaminopathy
|
Mfm Filamin C-Related
|
|
Myopathy Myofibrillar Filamin C-Related
|
Myopathy, Myofibrillar, Type 5
|
|
|
| Muscle Tissue Disease |
|
|
| Muscular Dystrophy, Duchenne Type |
|
Duchenne Muscular Dystrophy
|
DMD
|
|
Muscular Dystrophy, Duchenne
|
Muscular Dystrophy, Pseudohypertrophic Progressive, Duchenne Type
|
|
Severe Dystrophinopathy, Duchenne Type
|
Muscular Dystrophy Duchenne
|
|
Dystrophy, Muscular, Duchenne Type
|
Benign Duchenne Muscular Dystrophy
|
|
Duchenne Motor Neuron Disease
|
Duchenne Type Dystrophy
|
|
Duchenne-Griesinger Disease
|
|
|
| Cardiac Sarcoidosis |
|
|
| Myopathy, Spheroid Body |
|
Spheroid Body Myopathy
|
Autosomal Dominant Spheroid Body Myopathy
|
|
SBM
|
|
|
| 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
|
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Accessory Tricuspid Valve Tissue
|
Congenital Ebstein Deformity Of Tricuspid Valve
|
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Ebstein Syndrome
|
Ebstein Cardiopathy
|
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Ebstein Anomaly Of Tricuspid Valve
|
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| Myopathy, Centronuclear, X-Linked |
|
X-Linked Myotubular Myopathy
|
Xlmtm
|
|
X-Linked Centronuclear Myopathy
|
Xlcnm
|
|
CNMX
|
Mtm1
|
|
Myotubular Myopathy, X-Linked
|
Mtmx
|
|
Myotubular Myopathy 1
|
Centronuclear Myopathy X-Linked
|
|
Myotubular Myopathy
|
Mtm
|
|
Cnm
|
Xmtm
|
|
Myotubular Myopathy Type 1
|
|
|
| Mitral Valve Disease |
|
Chronic Rheumatic Mitral Valve
|
Rheumatic Mitral Insufficiency
|
|
Disease Of Mitral Valve
|
Mitral Rh Valve Dis.
|
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Rheumatic Disease Of Mitral Valve
|
Rheumatic Mitral Valve Changes
|
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Rheumatic Mitral Valve Incompetence
|
Rheumatic Mitral Valve Regurgitation
|
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Abnormality Of The Mitral Valve
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Diseases Of Mitral Valve
|
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Rheumatic Mitral Regurgitation
|
|
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| Mitral Valve Insufficiency |
|
Mitral Regurgitation
|
Congenital Insufficiency Of Mitral Valve
|
|
Congenital Mitral Insufficiency
|
Congenital Mitral Regurgitation
|
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Mitral Valve Incompetence
|
Mitral Valve Regurgitation
|
|
Mr - [Mitral Regurgitation]
|
Mi - [Mitral Incompetence]
|
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Mitral Valve Annular Incompetency
|
Congenital Mitral Valve Incompetence
|
|
Congenital Mitral Valve Insufficiency
|
Congenital Mitral Valve Regurgitation
|
|
Congenital Mitral Incompetence
|
|
|
| Muscular Dystrophy, Becker Type |
|
Becker Muscular Dystrophy
|
BMD
|
|
Benign Pseudohypertrophic Muscular Dystrophy
|
Benign Congenital Myopathy
|
|
Becker Dystrophinopathy
|
Becker'S Muscular Dystrophy
|
|
Muscular Dystrophy, Pseudohypertrophic Progressive, Becker Type
|
Muscular Dystrophy Pseudohypertrophic Progressive, Becker Type
|
|
Muscular Dystrophy Becker
|
Dystrophy, Muscular, Becker Type
|
|
Dystrophinopathy
|
Becker Dystrophy
|
|
Becker Type Dystrophy
|
Bmd - [Becker Muscular Dystrophy]
|
|
|
| Facioscapulohumeral Muscular Dystrophy 1 |
|
Facioscapulohumeral Muscular Dystrophy
|
Fshd
|
|
Landouzy-Dejerine Muscular Dystrophy
|
Muscular Dystrophy, Facioscapulohumeral
|
|
FSHD1
|
Fshd1a
|
|
Muscular Dystrophy, Facioscapulohumeral, Type 1a
|
Facioscapulohumeral Muscular Dystrophy Type 1a
|
|
Fsh Muscular Dystrophy
|
Facioscapulohumeral Muscular Dystrophy 1a
|
|
Facioscapulohumeral Atrophy
|
Facioscapulohumeral Myopathy
|
|
Muscular Dystrophy, Facioscapulohumeral, Type 1
|
Facioscapulohumeral Muscular Dystrophy Type 1
|
|
Landouzy Dejerine Muscular Dystrophy
|
Muscular Dystrophy, Landouzy-Dejerine
|
|
Fshmd1a
|
Facio-Scapulo-Humeral Dystrophy
|
|
Facioscapulohumeral Type Progressive Muscular Dystrophy
|
Facioscapuloperoneal Muscular Dystrophy
|
|
Facioscapulohumeral Dystrophy
|
Fsh Dystrophy
|
|
Landouzy-Dejerine Dystrophy
|
Landouzy-Dejerine Myopathy
|
|
Fmd
|
Facioscapulohumeral Muscular Dystrophy-1a
|
|
Muscular Dystrophy Facioscapulohumeral
|
Dystrophy, Muscular, Facioscapulohumeral
|
|
Dystrophy, Muscular, Facioscapulohumeral, Type 1
|
Landouzy-Dejerine Disease
|
|
Landouzy-Déjerine Atrophy
|
Facioscapulohumeral Muscle Dystrophy
|
|
Fmd - [Facioscapulohumeral Muscular Dystrophy]
|
Fsh - [Facioscapulohumeral Muscular Dystrophy]
|
|
Fshd - [Facioscapulohumeral Muscular Dystrophy]
|
Landouzy-Déjerine Dystrophy Or Facioscapulohumeral Atrophy
|
|
Landouzy-Déjérine Muscular Dystrophy
|
|
|
| Muscular Disease |
|
|
| Emery-Dreifuss Muscular Dystrophy |
|
Edmd
|
Emery-Dreifuss Syndrome
|
|
Muscular Dystrophy, Emery-Dreifuss
|
Humeroperoneal Neuromuscular Disease
|
|
Muscular Dystrophy, Tardive, Dreifuss-Emery Type, With Contractures
|
Scapuloperoneal Syndrome, X-Linked
|
|
Benign Scapuloperoneal Muscular Dystrophy With Early Contractures
|
Muscular Dystrophy, Emery-Dreifuss Type
|
|
Muscular Dystrophy Emery-Dreifuss
|
Dystrophy, Muscular, Emery-Dreifuss
|
|
Emd - [Emery-Dreifuss Muscular Dystrophy]
|
|
|
| Tricuspid Valve Disease |
|
Rheumatic Tricuspid Valve Disease
|
Disease Of Tricuspid Valve
|
|
Rh. Tricuspid Valve Disease
|
Rheumatic Disease Of Tricuspid Valve
|
|
Tricuspid Disease
|
Tricuspid Valve Disorder
|
|
|
| Neuromuscular Junction Disease |
|
Neuromuscular Junction Diseases
|
|
|
| Congenital Fiber-Type Disproportion |
|
Congenital Fiber Type Disproportion
|
Cftdm
|
|
Congenital Myopathy With Fiber Type Disproportion
|
Cftd
|
|
Congenital Fiber-Type Disproportion Myopathy
|
Fiber-Type Disproportion Myopathy, Congenital
|
|
Myopathy, Congenital With Fiber-Type Disproportion
|
|
|
| Extrinsic Cardiomyopathy |
|
|
| Barth Syndrome |
|
3-Methylglutaconic Aciduria Type 2
|
BTHS
|
|
Cardioskeletal Myopathy With Neutropenia And Abnormal Mitochondria
|
Mga Type Ii
|
|
Mga2
|
Mgca2
|
|
Mga Type 2
|
3-Methylglutaconic Aciduria Type Ii
|
|
3-Methylglutaconic Aciduria, Type Ii
|
Mga, Type Ii
|
|
3-Methylglutaconicaciduria Type 2
|
3-Methylglutaconicaciduria Type Ii
|
|
Taz Defect
|
3 Methylglutaconic Aciduria, Type Ii
|
|
Dnajc19 Defect
|
Cardioskeletal Myopathy-Neutropenia Syndrome
|
|
X-Linked Cardioskeletal Myopathy And Neutropenia
|
3-Alpha-Methylglutaconic Aciduria Type 2
|
|
Agm2
|
Cardioskeletal Myopathy-Neutropenia
|
|
Invm
|
Left Ventricular Non-Compaction Isolated X-Linked
|
|
Non-Compaction Of Left Ventricular Myocardium Isolated X-Linked
|
Agammaglobulinemia 2, Autosomal Recessive
|
|
|
| Autoimmune Disease |
|
Autoimmune Diseases
|
Autoimmune Hypersensitivity Disease
|
|
Hypersensitivity Reaction Type Ii Disease
|
Type Ii Hypersensitivity Reaction Disease
|
|
|
| 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
|
|
|
| Heart Valve Disease |
|
Heart Valve Diseases
|
Valvular Heart Disease
|
|
Valvular Heart Diseases
|
Heart Valve Prolapse
|
|
|
| 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
|
|
|
| Aortic Valve Disease 2 |
|
Aortic Valve Stenosis
|
Aortic Stenosis
|
|
Rheumatic Aortic Stenosis
|
AOVD2
|
|
Bicuspid Aortic Valve
|
Rheumatic Aortic Valve Stenosis
|
|
Valvular Aortic Stenosis
|
Aortic Valve Disease, Type 2
|
|
Aortic Valve Stricture
|
Aortic Valve Obstruction
|
|
Obstructed Aorta Valve
|
Rheumatic Aortic Obstruction
|
|
Rheumatic Aortic Valve Obstruction
|
Rheumatic Aortic Stricture
|
|
Aortic Valve Regurgitation
|
Aortic Insufficiency With Stenosis
|
|
Rheumatic Aortic Valve Stenosis With Insufficiency
|
Rheumatic Aortic Stenosis With Incompetence
|
|
Rheumatic Aortic Stenosis With Regurgitation
|
|
|
| Heart Conduction Disease |
|
Conduction Disorder Of The Heart
|
Heart Rhythm Disease
|
|
|
| Cardiac Tuberculosis |
|
Tuberculosis, Cardiovascular
|
Cardiovascular Tuberculosis
|
|
|
| Hypermethioninemia Due To Adenosine Kinase Deficiency |
|
Adk Hypermethioninemia
|
Hypermethioninemia Encephalopathy Due To Adenosine Kinase Deficiency
|
|
Hypermethioninemia Encephalopathy Due To Adk Deficiency
|
Mrt8
|
|
Mental Retardation, Autosomal Recessive 8, Formerly
|
Mrt8, Formerly
|
|
HMAKD
|
Mental Retardation, Autosomal Recessive 8
|
|
|
| Mitochondrial Dna Depletion Syndrome 12b |
|
|
| 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
|
|
|
| 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
|
|
|
| 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
|
|
|
| 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
|
|
|
| Myotonic Dystrophy 1 |
|
Myotonic Dystrophy
|
Dystrophia Myotonica
|
|
Steinert Disease
|
Myotonic Dystrophy Type 1
|
|
Myotonia Atrophica
|
DM1
|
|
Congenital Myotonic Dystrophy
|
Myotonia Dystrophica
|
|
Steinert Myotonic Dystrophy
|
Dystrophia Myotonica 1
|
|
Dm
|
Steinert'S Disease
|
|
Steinert Myotonic Dystrophy Syndrome
|
Myotonic Dystrophy Of Steinert
|
|
Dystrophia Myotonica Type 1
|
Myotonic Dystrophy Congenital
|
|
Dystrophy, Myotonic, Type 1
|
Dm - [Dystrophia Myotonica]
|
|
Myotonic Muscular Dystrophy
|
|
|
| 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
|
|
|
| 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
|
|
|
| Ptosis |
|
Blepharoptosis
|
Drooping Eyelid
|
|
Droopy Eyelid
|
Ptosis Of Eyelid
|
|
Paralysis Of Levator Palpebrae Superioris
|
|
|
| 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
|
|
|
| Long Qt Syndrome |
|
Romano-Ward Syndrome
|
Long Q-T Syndrome
|
|
Lqt
|
Qt Syndrome, Long
|
|
Congenital Long Qt Syndrome
|
Familial Long Qt Syndrome
|
|
|
| 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
|
|
|
| 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]
|
|
|
| Peripheral Nervous System Disease |
|
Peripheral Neuropathy
|
Peripheral Nerve Disease
|
|
Peripheral Nerve Disorders
|
Neuropathy, Peripheral
|
|
Peripheral Neuropathy Due To Vitamin Pyridoxine Hyperalimentation
|
|
|
