| Diseases |
Alias |
|
| Rippling Muscle Disease 2 |
|
Rippling Muscle Disease
|
Rmd
|
|
Lgmd1c
|
RMD2
|
|
Autosomal Dominant Limb-Girdle Muscular Dystrophy Type 1c
|
Muscular Dystrophy, Limb-Girdle, Type 1c
|
|
Muscular Dystrophy, Limb-Girdle, Type 1c, Formerly
|
Lgmd1c, Formerly
|
|
Limb-Girdle Muscular Dystrophy Type 1c
|
Limb-Girdle Muscular Dystrophy Due To Caveolin-3 Deficiency
|
|
Muscular Dystrophy, Limb-Girdle, Type Ic
|
Rippling Muscle Syndrome
|
|
Limb-Girdle Muscular Dystrophy 1c
|
Dystrophy, Muscular, Limb-Girdle, Type 1c
|
|
Disease, Muscle, Rippling, Type 2
|
Rippling Muscle Disease 1
|
|
|
| Myopathy, Distal, Tateyama Type |
|
Distal Myopathy, Tateyama Type
|
MPDT
|
|
Cav3-Related Distal Myopathy
|
|
|
| Long Qt Syndrome 9 |
|
LQT9
|
Long Qt Syndrome-9
|
|
Qt Syndrome, Long, Type 9
|
|
|
| Creatine Phosphokinase, Elevated Serum |
|
Hyperckemia, Idiopathic
|
Cpk, Elevated Serum
|
|
Hyperckmia
|
HYPCK
|
|
|
| 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
|
|
|
| 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
|
|
|
| Isolated Asymptomatic Elevation Of Creatine Phosphokinase |
|
Idiopathic Asymptomatic Hyperckemia
|
Isolated Asymptomatic Hyperckemia
|
|
|
| Long Qt Syndrome |
|
Romano-Ward Syndrome
|
Long Q-T Syndrome
|
|
Lqt
|
Qt Syndrome, Long
|
|
Congenital Long Qt Syndrome
|
Familial Long Qt 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
|
|
|
| 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
|
|
|
| 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
|
|
|
| Miyoshi Muscular Dystrophy |
|
Distal Myopathy
|
Distal Muscular Dystrophy
|
|
Miyoshi Myopathy
|
Distal Myopathies
|
|
Dystrophy, Muscular, Miyoshi
|
Myopathy, Distal
|
|
Distal Muscular Dystrophies
|
|
|
| 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, 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
|
|
|
| Limb-Girdle Muscular Dystrophy Type 1b |
|
Lgmd1b
|
Muscular Dystrophy, Proximal, Type 1b
|
|
Limb-Girdle Muscular Dystrophy, Type 1b
|
|
|
| Long Qt Syndrome 12 |
|
LQT12
|
Qt Syndrome, Long, Type 12
|
|
|
| Myopathy |
|
Muscular Diseases
|
Myopathies
|
|
|
| Long Qt Syndrome 10 |
|
LQT10
|
Atrial Fibrillation, Familial, 17
|
|
ATFB17
|
Long Qt Syndrome-10
|
|
Qt Syndrome, Long, Type 10
|
|
|
| Muscular Atrophy |
|
Muscle Wasting
|
Amyotrophia
|
|
Wasting - Muscle
|
Skeletal Muscle Atrophy
|
|
|
| Lipodystrophy, Congenital Generalized, Type 4 |
|
Congenital Generalized Lipodystrophy Type 4
|
CGL4
|
|
Berardinelli-Seip Congenital Lipodystrophy, Type 4, With Muscular Dystrophy
|
Lipodystrophy, Berardinelli-Seip Congenital, Type 4, With Muscular Dystrophy
|
|
Berardinelli-Seip Congenital Lipodystrophy Type 4 With Muscular Dystrophy
|
Generalized Congenital Lipodystrophy With Myopathy
|
|
Congenital Generalised Lipodystrophy Type 4
|
Generalised Congenital Lipodystrophy Type 4
|
|
Generalised Congenital Lipodystrophy With Myopathy
|
Generalized Congenital Lipodystrophy Type 4
|
|
Gcl4
|
Congenital Generalized Lipodystrophy 4
|
|
Berardinelli-Seip Congenital Lipodystrophy Type 4
|
|
|
| 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
|
|
|
| Progressive Muscular Atrophy |
|
Progressive Spinal Muscular Atrophy
|
Pure Progressive Muscular Atrophy
|
|
Pma
|
Hereditary Spinal Muscle Atrophy
|
|
Pma - [Progressive Muscular Atrophy]
|
Progressive Muscle Atrophy
|
|
Progressive Spinal Muscle Atrophy
|
Duchenne-Aran Atrophy
|
|
Duchenne-Aran Muscle Atrophy
|
Hereditary Sma - [Spinal Muscle Atrophy]
|
|
|
| Centronuclear Myopathy |
|
Myopathy, Centronuclear
|
Myotubular Myopathy
|
|
Cnm
|
Myopathy, Myotubular
|
|
Congenital Structural Myopathy
|
|
|
| Autosomal Dominant Limb-Girdle Muscular Dystrophy |
|
Muscular Dystrophy, Limb-Girdle, Autosomal Dominant
|
|
|
| Muscular Dystrophy, Limb-Girdle, Autosomal Dominant 2 |
|
Muscular Dystrophy, Limb-Girdle, Type 1f
|
Lgmd1f
|
|
Autosomal Dominant Limb-Girdle Muscular Dystrophy Type 1f
|
LGMDD2
|
|
Autosomal Dominant Limb-Girdle Muscular Dystrophy Type 2
|
Muscular Dystrophy Limb-Girdle Type 1f
|
|
Tnp03-Related Limb-Girdle Muscular Dystrophy D2
|
Lgmd Type 1f
|
|
Limb-Girdle Muscular Dystrophy Type 1f
|
Limb-Girdle Muscular Dystrophy 1f
|
|
Dystrophy, Muscular, Limb-Girdle, Type 1f
|
|
|
| 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
|
|
|
| Muscular Dystrophy, Limb-Girdle, Type 1h |
|
Autosomal Dominant Limb-Girdle Muscular Dystrophy Type 1h
|
LGMD1H
|
|
Muscular Dystrophy Limb-Girdle Type 1h
|
Dystrophy, Muscular, Limb-Girdle, Type 1h
|
|
|
| Muscular Dystrophy, Limb-Girdle, Autosomal Dominant 3 |
|
Lgmd1g
|
Autosomal Dominant Limb-Girdle Muscular Dystrophy Type 1g
|
|
LGMDD3
|
Muscular Dystrophy, Limb-Girdle, Type 1g
|
|
Autosomal Dominant Limb-Girdle Muscular Dystrophy Type 3
|
Limb-Girdle Muscular Dystrophy, Type 1g
|
|
Muscular Dystrophy Limb-Girdle Type 1g
|
Hnrnpdl-Related Limb-Girdle Muscular Dystrophy D3
|
|
Hnrnpdl-Related Lgmd D3
|
Lgmd Type 1g
|
|
Limb-Girdle Muscular Dystrophy Type 1g
|
Limb-Girdle Muscular Dystrophy 1g
|
|
Dystrophy, Muscular, Limb-Girdle, Type 1g
|
|
|
| Long Qt Syndrome 11 |
|
LQT11
|
Long Qt Syndrome-11
|
|
Qt Syndrome, Long, Type 11
|
|
|
| Timothy Syndrome |
|
Long Qt Syndrome With Syndactyly
|
TS
|
|
Lqt8
|
Long Qt Syndrome 8
|
|
Long Qt Syndrome Type 8
|
Long Qt Syndrome-Syndactyly Syndrome
|
|
|
| Uruguay Faciocardiomusculoskeletal Syndrome |
|
FCMSU
|
Faciocardiomusculoskeletal Syndrome, Uruguay Type
|
|
Fcms
|
Musculoskeletal Diseases
|
|
|
| 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 2b |
|
Lgmd2b
|
Lgmd3
|
|
Limb-Girdle Muscular Dystrophy Due To Dysferlin Deficiency
|
Limb-Girdle Muscular Dystrophy Type 3
|
|
Muscular Dystrophy, Limb-Girdle, Type 2b
|
|
|
| Long Qt Syndrome 3 |
|
LQT3
|
Long Qt Syndrome Type 3
|
|
Long Qt Syndrome-3
|
Qt Syndrome, Long, Type 3
|
|
|
| Long Qt Syndrome 6 |
|
LQT6
|
Long Qt Syndrome 3/6
|
|
Lqt3/6
|
Susceptibility To Acquired Long Qt Syndrome 6
|
|
Long Qt Syndrome-6
|
Long Qt Syndrome 6, Acquired, Susceptibility To
|
|
Qt Syndrome, Long, Type 6
|
Long Qt Syndrome 3-6
|
|
|
| Long Qt Syndrome 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
|
|
|
| Muscular Dystrophy, Limb-Girdle, Autosomal Dominant 1 |
|
Muscular Dystrophy, Limb-Girdle, Type 1e
|
Lgmd1d
|
|
Autosomal Dominant Limb-Girdle Muscular Dystrophy Type 1d
|
LGMDD1
|
|
Lgmd1e
|
Autosomal Dominant Limb-Girdle Muscular Dystrophy Type 1
|
|
Limb-Girdle Muscular Dystrophy Type 1d
|
Muscular Dystrophy, Limb-Girdle, Type 1d
|
|
Muscular Dystrophy, Limb-Girdle, Type 1d, Formerly
|
Lgmd1d, Formerly
|
|
Autosomal Dominant Limb-Girdle Muscular Dystrophy Type 1e
|
Muscular Dystrophy Limb-Girdle Type 1d
|
|
Muscular Dystrophy Limb-Girdle Type 1e
|
Dnajb6-Related Limb-Girdle Muscular Dystrophy D1
|
|
Dnajb6-Related Lgmd D1
|
Lgmd Type 1d
|
|
Limb-Girdle Muscular Dystrophy 1e
|
Limb-Girdle Muscular Dystrophy-1d, Autosomal Dominant
|
|
Dystrophy, Muscular, Limb-Girdle, Autosomal Dominant, Type 1
|
Dystrophy, Muscular, Limb-Girdle, Type 1e
|
|
|
| Neuromuscular Disease |
|
Neuromuscular Diseases
|
Neuromuscular Disorders
|
|
Neuromuscular Disorder
|
|
|
| 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
|
|
|
| Long Qt Syndrome 13 |
|
LQT13
|
Qt Syndrome, Long, Type 13
|
|
|
| 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
|
|
|
| Autosomal Recessive Limb-Girdle Muscular Dystrophy Type 2f |
|
Delta-Sarcoglycanopathy
|
Lgmd2f
|
|
Limb-Girdle Muscular Dystrophy Due To Delta-Sarcoglycan Deficiency
|
Limb-Girdle Muscular Dystrophy Type 2f
|
|
|
| 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
|
|
|
| Autosomal Recessive Limb-Girdle Muscular Dystrophy Type 2x |
|
Lgmd2x
|
Muscular Dystrophy, Limb-Girdle, Type 2x
|
|
|
| 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
|
|
|
| Autosomal Recessive Limb-Girdle Muscular Dystrophy |
|
Muscular Dystrophy, Limb-Girdle, Autosomal Recessive
|
|
|
| Rhabdomyosarcoma |
|
|
| Autosomal Recessive Limb-Girdle Muscular Dystrophy Type 2j |
|
Lgmd2j
|
Muscular Dystrophy, Limb-Girdle, Type 2j
|
|
|
| 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
|
|
|
| Autosomal Recessive Limb-Girdle Muscular Dystrophy Type 2d |
|
Alpha-Sarcoglycanopathy
|
Dmda2
|
|
Duchenne-Like Autosomal Recessive Muscular Dystrophy Type 2
|
Lgmd2d
|
|
Muscular Dystrophy, Limb-Girdle, Type 2d
|
Primary Adhalinopathy
|
|
|
| Glycogen Storage Disease Ii |
|
Pompe Disease
|
Glycogen Storage Disease Type Ii
|
|
Acid Maltase Deficiency
|
Gsd Ii
|
|
Gaa Deficiency
|
Alpha-1,4-Glucosidase Deficiency
|
|
Glycogenosis Type Ii
|
GSD2
|
|
Acid Alpha-Glucosidase Deficiency
|
Amd
|
|
Glycogen Storage Disease, Type Ii
|
Pompe'S Disease
|
|
Glycogen Storage Disease Type 2
|
Cardiomegalia Glycogenica Diffusa
|
|
Acid Maltase Deficiency Disease
|
Deficiency Of Alpha-Glucosidase
|
|
Glycogenosis, Generalized, Cardiac Form
|
Deficiency Of Glucoamylase
|
|
Deficiency Of Maltase
|
Generalized Glycogenosis
|
|
Glycogenosis, Type 2
|
Lysosomal Alpha-1,4-Glucosidase Deficiency
|
|
Glucosidase Acid-1,4-Alpha Deficiency
|
Aglucosidase Alfa
|
|
Deficiency Of Lysosomal Alpha-Glucosidase
|
Glycogen Storage Disease Due To Acid Maltase Deficiency
|
|
Alpha-1,4-Glucosidase Acid Deficiency
|
Gsd Due To Acid Maltase Deficiency
|
|
Gsd Type 2
|
Gsd Type Ii
|
|
Glycogenosis Due To Acid Maltase Deficiency
|
Glycogenosis Type 2
|
|
Glycogen Storage Disease 2
|
Cardiomegalia Glycogenica
|
|
Glycogenosis Generalized Cardiac Form
|
Glycogenosis Ii
|
|
Gsd-Ii
|
Storage Disease, Glycogen, Type Ii
|
|
Generalized Glycogen Storage Disease Of Infants
|
Cardiac Form Of Generalized Glycogenosis
|
|
|
| Cardiomyopathy, Dilated, 3b |
|
Dilated Cardiomyopathy 3b
|
CMD3B
|
|
X-Linked Dilated Cardiomyopathy
|
Xlcm
|
|
Dmd-Associated Dilated Cardiomyopathy
|
Cardiomyopathy, Dilated, X-Linked
|
|
Dmd-Related Dilated Cardiomyopathy
|
Xldc
|
|
Cardiomyopathy, Dilated, X-Linked 3b
|
Cardiomyopathy, Dilated, Type 3b
|
|
|
| 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]
|
|
|
| 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
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Familial Ventricular Tachycardia
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Multifocal Pvcs
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Multifocal Premature Ventricular Beats
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| Intrinsic Cardiomyopathy |
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| Muscular Dystrophy, Congenital, Lmna-Related |
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Congenital Muscular Dystrophy
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Congenital Muscular Dystrophy Due To Lmna Mutation
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MDCL
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L-Cmd
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Lmna-Related Congenital Muscular Dystrophy
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Muscular Dystrophy, Congenital
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Congenital Muscular Dystrophy Lmna-Related
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Lmna-Related Cmd
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Cmd
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Mdc
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Muscular Dystrophy Congenital Lmna-Related
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Dystrophy, Muscular, Congenital, Lmna-Related
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Dystrophy, Muscular, Congenital
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Hereditary Muscular Dystrophy
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Congenital Hereditary Muscular Dystrophy
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Congenital Progressive Muscular Dystrophy
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Hereditary Progressive Muscular Dystrophy
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| Tibial Muscular Dystrophy |
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Tmd
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Udd Myopathy
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Distal Titinopathy
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Finnish Tibial Muscular Dystrophy
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Tardive Tibial Muscular Dystrophy
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Udd Type Distal Myopathy
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Udd Distal Myopathy
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Udd-Markesbery Muscular Dystrophy
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Distal Myopathy, Udd Type
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Distal Myopathies
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Tibial Muscular Dystrophy, Tardive
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| Muscle Tissue Disease |
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| Jervell And Lange-Nielsen Syndrome 1 |
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Jervell And Lange-Nielsen Syndrome
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Jervell-Lange Nielsen Syndrome
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Prolonged Qt Interval In Ekg And Sudden Death
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Cardioauditory Syndrome Of Jervell And Lange-Nielsen
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Surdo-Cardiac Syndrome
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JLNS1
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Deafness, Congenital, And Functional Heart Disease
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Jlns
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Long Qt Interval-Deafness Syndrome
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Jervell And Lange-Nielson Syndrome
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Jervell Lange-Nielsen Syndrome
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Autosomal Recessive Long Qt Syndrome
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Cardio-Auditory-Syncope Syndrome
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Long Qt Interval-Hearing Loss Syndrome
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Congenital Deafness And Functional Heart Disease
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Long Qt Interval-Deafness
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| Hypokalemic Periodic Paralysis, Type 1 |
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Hypokalemic Periodic Paralysis
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Hokpp
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Hypopp
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Westphall Disease
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HOKPP1
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Familial Hypokalemic Periodic Paralysis
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Familial Periodic Paralysis
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Westphal Disease
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Hypokalemic Periodic Paralysis Type 1
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Hypokalemic Familial Periodic Paralysis
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Periodic Hypokalemic Paralysis
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Periodic Paralysis I
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Hypokpp
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Primary Hypokalemic Periodic Paralysis
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Periodic Paralysis Hypokalemic 1
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Paralysis, Hypokalemic, Periodic
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Paralysis, Hypokalemic, Periodic, Type 1
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| Childhood Absence Epilepsy |
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Pyknolepsy
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Petit Mal Epilepsy
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Absence Seizures
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Absence Seizure
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Petit Mal Seizure
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Absence Epilepsy, Childhood
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Pykno-Epilepsy
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Epilepsy, Absence
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Absence Epilepsy
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Pycnolepsy
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| Muscular Disease |
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| Congenital Generalized Lipodystrophy |
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Berardinelli-Seip Congenital Lipodystrophy
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Berardinelli-Seip Syndrome
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Brunzell Syndrome
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Bscl
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Generalized Lipodystrophy
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Lipodystrophy, Congenital Generalized
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Seip Syndrome
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Total Lipodystrophy
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Cgl
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Lipoatrophic Diabetes
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Lipodystrophy, Generalized, Congenital
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Familial Generalized Lipodystrophy
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Congenital Generalized Lipodystrophy Type 2
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Lipoatrophic Diabetes Mellitus
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Familial Partial Lipodystrophy, Type 2
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| Myofibrillar Myopathy |
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Desmin Related Myopathy
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Myotilinopathy
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Myopathy, Myofibrillar
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Alpha Beta Crystallinopathy
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Desmin Storage Myopathy
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Desminopathy
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Filaminopathy
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Protein Surplus Myopathy
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Zaspopathy
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Myofibrillar Myopathies
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Myopathy, Myofibrillar, Desmin-Related
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Myopathy, Desmin Storage
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Mfm - [Myofibrillar Myopathy]
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| Malignant Hyperthermia |
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Anesthesia Related Hyperthermia
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Malignant Hyperpyrexia Due To Anesthesia
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Hyperpyrexia, Malignant
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Hyperthermia, Malignant
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Malignant Hyperpyrexia
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Mhs
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Malignant Fever
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| Episodic Ataxia |
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Isaacs Syndrome
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Neuromyotonia
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Isaacs' Syndrome
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Acquired Neuromyotonia
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Continuous Muscle Fiber Activity Syndrome
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Quantal Squander Syndrome
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Isaacs-Mertens Syndrome
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Ea Syndrome
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Episodic Ataxia Syndrome
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Isaac Syndrome
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Isaac'S-Merten'S Syndrome
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Isaac-Mertens Syndrome
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Peripheral Nerve Hyperexcitability
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Ea
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Peripheral Nerve Hyperexcitability Syndrome
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Ataxia, Episodic
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Isaacs Neuromyotonia
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Continuous Muscle Fibre Activity
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| Bethlem Myopathy 1 |
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Bethlem Myopathy
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Myopathy, Benign Congenital, With Contractures
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Muscular Dystrophy, Benign Congenital
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BTHLM1
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Muscular Dystrophy, Limb-Girdle, Autosomal Dominant 5
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Lgmdd5
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Benign Congenital Muscular Dystrophy
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Benign Autosomal Dominant Myopathy
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Myopathy, Bethlem
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Myopathy, Bethlem, Type 1
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| Walker-Warburg Syndrome |
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Hard Syndrome
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Walker-Warburg Congenital Muscular Dystrophy
|
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Cerebroocular Dysplasia-Muscular Dystrophy Syndrome
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Cod-Md Syndrome
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Chemke Syndrome
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Hydrocephalus, Agyria And Retinal Dysplasia
|
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Cerebroocular Dysgenesis
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Cerebroocular Dysplasia Muscular Dystrophy Syndrome
|
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Hard +/- E Syndrome
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Pagon Syndrome
|
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Warburg Syndrome
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Hydrocephalus, Agyria, And Retinal Dysplasia
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Mddga
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Muscular Dystrophy-Dystroglycanopathy , Type A
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Muscular Dystrophy-Dystroglycanopathy [With Brain And Eye Anomalies], Type A
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Hydrocephalus-Agyria-Retinal Dysplasia Syndrome
|
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Wws
|
Dystrophy, Muscular, Dystroglycanopathy, Type A
|
|
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| Hypertrophic Cardiomyopathy |
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Hypertrophic Obstructive Cardiomyopathy
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Cardiomyopathy, Hypertrophic
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Cardiomyopathy Hypertrophic Obstructive
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Cardiomyopathy, Hypertrophic, Familial
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Idiopathic Myocardial Hypertrophy
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Idiopathic Hypertrophic Cardiomyopathy
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Obstructive Idiopathic Hypertrophic Cardiomyopathy
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Obstructive Cardiomyopathy
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Idiopathic Hypertrophic Subaortic Stenosis
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Muscular Subaortic Stenosis
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Hypertrophic Obstructive Subaortic Stenosis
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| Left Ventricular Noncompaction |
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Noncompaction Cardiomyopathy
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Left Ventricular Hypertrabeculation
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Lvnc
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Spongy Myocardium
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Isolated Noncompaction Of The Ventricular Myocardium
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Left Ventricular Myocardial Noncompaction Cardiomyopathy
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Fetal Myocardium
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Honeycomb Myocardium
|
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Hypertrabeculation Syndrome
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Left Ventricular Non-Compaction
|
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Lvht
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Non-Compaction Of The Left Ventricular Myocardium
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Ventricular Noncompaction, Left
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Non-Compaction Cardiomyopathy
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| Dilated Cardiomyopathy |
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Familial Dilated Cardiomyopathy
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Primary Dilated Cardiomyopathy
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Idiopathic Dilated Cardiomyopathy
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Congestive Cardiomyopathy
|
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Idiopathic Dilation Cardiomyopathy
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Primary Familial Dilated Cardiomyopathy
|
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Cardiomyopathy, Dilated
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DCM
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Cardiomyopathy, Familial Dilated
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Dilated Cardiomyopathy, Familial
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Hypokinetic Dilated Cardiomyopathy, Familial
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Familial Idiopathic Cardiomyopathy
|
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Fdc
|
Cardiomyopathy, Familial Idiopathic
|
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Idiopathic Cardiomegaly
|
Dilated Congestive Cardiomyopathy
|
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Chronic Dilated Cardiomyopathy
|
Ccm - [Congestive Cardiomyopathy]
|
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Cocm - [Congestive Cardiomyopathy]
|
Dcm - [Dilated Cardiomyopathy]
|
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Dilated-Hypokinetic Cardiomyopathy
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Congestive Idiopathic Cardiomyopathy
|
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Primary Idiopathic Dilated Cardiomyopathy
|
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