| Diseases |
Alias |
|
| Myopathy, Distal, 4 |
|
Distal Myopathy With Posterior Leg And Anterior Hand Involvement
|
MPD4
|
|
Williams Distal Myopathy
|
Distal Muscular Dystrophy 4
|
|
Distal Abd-Filaminopathy
|
Distal Myopathy 4
|
|
Myopathy, Distal, Type 4
|
|
|
| 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
|
|
|
| Cardiomyopathy, Familial Hypertrophic, 26 |
|
Hypertrophic Cardiomyopathy 26
|
CMH26
|
|
Cardiomyopathy, Familial Restrictive 5
|
Cardiomyopathy, Familial Restrictive, 5
|
|
Cardiomyopathy Familial Hypertrophic 26
|
Cardiomyopathy, Familial Hypertrophic 26
|
|
RCM5
|
|
|
| Familial Isolated Restrictive Cardiomyopathy |
|
Familial Or Idiopathic Restrictive Cardiomyopathy
|
|
|
| Restrictive Cardiomyopathy |
|
Familial Restrictive Cardiomyopathy
|
Cardiomyopathy, Restrictive
|
|
Cardiomyopathy, Constrictive
|
Primary Restrictive Cardiomyopathy
|
|
Rcm
|
Cardiomyopathy Restrictive
|
|
|
| Hemifacial Hyperplasia |
|
Hemifacial Hypertrophy
|
Facial Asymmetry
|
|
Facial Hemihypertrophy
|
Asymmetric Face
|
|
|
| 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]
|
|
|
| Patent Foramen Ovale |
|
Atrial Septal Defect Within Oval Fossa
|
Foramen Ovale Patent
|
|
Ostium Secundum Atrial Septal Defect
|
Atrial Septal Defect, Ostium Secundum Type
|
|
Foramen Ovale, Patent
|
Defect, Patent Or Persistent, Ostium Secundum
|
|
Ostium Secundum Type Atrial Septal Defect
|
Persistent Ostium Secundum
|
|
Asd Ostium Secundum Type
|
Ostium Secundum Asd
|
|
Osasd
|
Asd, Ostium Secundum Type
|
|
Pfo - [Patent Foramen Ovale]
|
Open Foramen Ovale
|
|
Open Oval Foramen
|
Persistent Foramen Ovale
|
|
Secundum Atrial Septal Defect
|
|
|
| Dilated Cardiomyopathy |
|
Familial Dilated Cardiomyopathy
|
Primary Dilated Cardiomyopathy
|
|
Idiopathic Dilated Cardiomyopathy
|
Congestive Cardiomyopathy
|
|
Idiopathic Dilation Cardiomyopathy
|
Primary Familial Dilated Cardiomyopathy
|
|
Cardiomyopathy, Dilated
|
DCM
|
|
Cardiomyopathy, Familial Dilated
|
Dilated Cardiomyopathy, Familial
|
|
Hypokinetic Dilated Cardiomyopathy, Familial
|
Familial Idiopathic Cardiomyopathy
|
|
Fdc
|
Cardiomyopathy, Familial Idiopathic
|
|
Idiopathic Cardiomegaly
|
Dilated Congestive Cardiomyopathy
|
|
Chronic Dilated Cardiomyopathy
|
Ccm - [Congestive Cardiomyopathy]
|
|
Cocm - [Congestive Cardiomyopathy]
|
Dcm - [Dilated Cardiomyopathy]
|
|
Dilated-Hypokinetic Cardiomyopathy
|
Congestive Idiopathic Cardiomyopathy
|
|
Primary Idiopathic Dilated Cardiomyopathy
|
|
|
| Spastic Ataxia |
|
|
| Aceruloplasminemia |
|
Cerebellar Ataxia
|
Hypoceruloplasminemia
|
|
Hemosiderosis, Systemic, Due To Aceruloplasminemia
|
Familial Apoceruloplasmin Deficiency
|
|
Hereditary Ceruloplasmin Deficiency
|
Deficiency Of Ferroxidase
|
|
Hypoceruloplasminemia, Hereditary
|
Ceruloplasmin Deficiency
|
|
Systemic Hemosiderosis Due To Aceruloplasminemia
|
ACERULOP
|
|
|
| Heart Conduction Disease |
|
Conduction Disorder Of The Heart
|
Heart Rhythm Disease
|
|
|
| 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
|
|
|
| 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
|
|
|
| Cardiomyopathy, Dilated, 1b |
|
Cardiomyopathy, Familial Dilated, 1
|
Cardiomyopathy, Dilated 1b
|
|
CMD1B
|
Cmpd1
|
|
Cardiomyopathy, Familial Dilated
|
Fdc
|
|
Dilated Cardiomyopathy 1b
|
Familial Dilated Cardiomyopathy
|
|
|
| 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
|
|
|
| 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 |
|
Muscular Diseases
|
Myopathies
|
|
|
| Boomerang Dysplasia |
|
BOOMD
|
Boomerang-Like Skeletal Dysplasia
|
|
Dwarfism With Short, Bowed, Rigid Limbs And Characteristic Facies
|
Piepkorn Dysplasia
|
|
Dysplasia, Boomerang
|
|
|
| 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
|
|
|
| Inclusion Body Myopathy With Early-Onset Paget Disease Of Bone With Or Without Frontotemporal Dementia 2 |
|
Ibmpfd2
|
Msp2
|
|
Multisystem Proteinopathy 2
|
|
|
| Cardiomyopathy, Familial Restrictive, 2 |
|
RCM2
|
Restrictive Cardiomyopathy 2
|
|
Familial Restrictive Cardiomyopathy 2
|
Cardiomyopathy, Restrictive, Familial, Type 2
|
|
|
| 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
|
|
|
| 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
|
|
|
| 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
|
|
|
| Melnick-Needles Syndrome |
|
MNS
|
Melnick-Needles Osteodysplasty
|
|
Osteodysplasty Of Melnick And Needles
|
Osteochondrodysplasias
|
|
|
| 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
|
|
|
| Myopathy, Myofibrillar, 4 |
|
Myofibrillar Myopathy 4
|
MFM4
|
|
Zaspopathy
|
Myopathy, Myofibrillar, Zasp-Related
|
|
|
| Myopathy, Spheroid Body |
|
Spheroid Body Myopathy
|
Autosomal Dominant Spheroid Body Myopathy
|
|
SBM
|
|
|
| Crab Allergy |
|
Green Mud Crab Allergy
|
Scylla Paramamosain Allergy
|
|
|
| Miyoshi Muscular Dystrophy |
|
Distal Myopathy
|
Distal Muscular Dystrophy
|
|
Miyoshi Myopathy
|
Distal Myopathies
|
|
Dystrophy, Muscular, Miyoshi
|
Myopathy, Distal
|
|
Distal Muscular Dystrophies
|
|
|
| Atelosteogenesis |
|
|
| Otopalatodigital Syndrome Spectrum Disorder |
|
Opd Spectrum Disorder
|
Opsd
|
|
Fronto-Otopalatodigital Osteodysplasia
|
|
|
| Autosomal Dominant Limb-Girdle Muscular Dystrophy |
|
Muscular Dystrophy, Limb-Girdle, Autosomal Dominant
|
|
|
| Frontometaphyseal Dysplasia |
|
Fmd
|
Dysplasia, Frontometaphyseal
|
|
|
| Postural Orthostatic Tachycardia Syndrome |
|
Irritable Heart
|
Mitral Valve Prolapse Syndrome
|
|
Neurocirculatory Asthenia
|
Orthostatic Intolerance Due To Net Deficiency
|
|
Familial Orthostatic Tachycardia Due To Norepinephrine Transporter Deficiency
|
Orhtostatic Intolerance
|
|
Postural Tachycardia Syndrome Due To Net Deficiency
|
Soldiers Heart
|
|
|
| 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
|
|
|
| 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
|
|
|
| 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
|
|
|
| Myopathy, Myofibrillar, 8 |
|
Myofibrillar Myopathy 8
|
MFM8
|
|
Myopathy, Myofibrillar, Type 8
|
|
|
| Otopalatodigital Syndrome, Type Ii |
|
Otopalatodigital Syndrome Type 2
|
Faciopalatoosseous Syndrome
|
|
OPD2
|
Opd Ii Syndrome
|
|
Opd Syndrome 2
|
Cranioorodigital Syndrome
|
|
Fpo
|
Oto-Palato-Digital Syndrome, Type Ii
|
|
Andre Syndrome
|
Oto-Palato-Digital Syndrome Type 2
|
|
Otopalatodigital Syndrome Type Ii
|
Cranio-Oro-Digital Syndrome
|
|
Opd 2 Syndrome
|
Opd Syndrome, Type 2
|
|
Taybi Syndrome
|
Otopalatodigital Syndrome 2
|
|
Oto-Palato-Digital Syndrome, Type 2
|
Oto-Palato-Digital Syndrome Type 1
|
|
|
| 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
|
|
|
| Scapuloperoneal Myopathy |
|
|
| Myopathy, Myofibrillar, 7 |
|
Myofibrillar Myopathy 7
|
MFM7
|
|
Kyphosis-Lateral Tongue Atrophy-Myofibrillar Myopathy Syndrome
|
Myopathy, Myofibrillar, Type 7
|
|
|
| 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
|
|
|
| Mitochondrial Dna Depletion Syndrome 12b |
|
|
| 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
|
|
|
| Xanthomatosis |
|
Xanthomatosis, Susceptibility To
|
Xanthelasmatosis
|
|
|
| Gastric Cancer |
|
Stomach Cancer
|
Gastric Carcinoma
|
|
Stomach Carcinoma
|
Gastric Cancer, Somatic
|
|
Gastric Neoplasm
|
Carcinoma Of Stomach
|
|
Stomach Neoplasms
|
Malignant Neoplasm Of Stomach
|
|
Gastric Cancer Risk After H. Pylori Infection
|
Cancer Of The Stomach
|
|
Adult Stomach Cancer
|
Adult Stomach Carcinoma
|
|
GASC
|
Gastric Cancer Intestinal
|
|
Gastric Cancers
|
Gastric Carcinomas
|
|
Cancer, Gastric
|
Stomach Neoplasm
|
|
Malignant Neoplasm Of Body Of Stomach
|
Malignant Tumor Of Lesser Curve Of Stomach
|
|
Gastrocarcinoma Of Unspecified Site
|
Leather Bottle Stomach
|
|
Carcinoma Of Fundus Of Stomach
|
Cancer Of Fundus Of Stomach
|
|
Primary Malignant Neoplasm Of Body Of Stomach
|
Cancer Of Body Of Stomach
|
|
Primary Malignant Neoplasm Of Pyloric Antrum
|
Pyloric Antrum Cancer
|
|
Malignant Tumour Of Stomach
|
|
|
| Hyaline Body Myopathy |
|
Myosin Storage Myopathy
|
Autosomal Dominant Hyaline Body Myopathy
|
|
Myopathy, Myosin Storage
|
|
|
| Myopathy, Centronuclear, 5 |
|
CNM5
|
Centronuclear Myopathy 5
|
|
Myopathy, Centronuclear, Type 5
|
|
|
| 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
|
|
|
| Cardiac Sarcoidosis |
|
|
| 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
|
|
|
| Larsen Syndrome |
|
LRS
|
Larsen Syndrome, Dominant Type
|
|
Dominant Larsen Syndrome
|
Autosomal Dominant Larsen Syndrome
|
|
Larsens Syndrome
|
|
|
| Periventricular Nodular Heterotopia |
|
Periventricular Heterotopia
|
Pvnh
|
|
Familial Nodular Heterotopia
|
Heterotopia, Periventricular
|
|
Periventricular Heterotopia, X-Linked
|
|
|
| Autosomal Recessive Limb-Girdle Muscular Dystrophy Type 2j |
|
Lgmd2j
|
Muscular Dystrophy, Limb-Girdle, Type 2j
|
|
|
| Congenital Structural Myopathy |
|
|
| Terminal Osseous Dysplasia |
|
Terminal Osseous Dysplasia And Pigmentary Defects
|
Terminal Osseous Dysplasia-Pigmentary Defects Syndrome
|
|
Todpd
|
TOD
|
|
Odpd
|
Odpf Syndrome
|
|
Osseous Dysplasia, Digital, With Facial Pigmentary Defects And Multiple Frenula
|
Odpf
|
|
Digital Osseous Dysplasia With Facial Pigmentary Defects And Multiple Frenula
|
Terminal Osseous Dysplasia With Pigmentary Defects
|
|
Dcd
|
Digitocutaneous Dysplasia
|
|
Terminal Osseous Dysplasia And Pigmentary Defect Syndrome
|
Osseous Dysplasia And Pigmentary Defects
|
|
|
| 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
|
|
|
| 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
|
|
|
| Intrinsic Cardiomyopathy |
|
|
| Batten-Turner Congenital Myopathy |
|
Congenital Myopathy
|
Batten Turner Congenital Myopathy
|
|
Myopathy Congenital
|
Myopathy, Congenital
|
|
Myotonia Congenita
|
Benign Congenital Myopathy
|
|
|
| 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
|
|
|
| Autosomal Recessive Limb-Girdle Muscular Dystrophy |
|
Muscular Dystrophy, Limb-Girdle, Autosomal Recessive
|
|
|
| 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
|
|
|
| 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
|
|
|
| Muscle Tissue Disease |
|
|
| 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
|
|
|
| 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
|
|
|
| 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
|
|
|
| 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 |
|
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]
|
|
|
| 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
|
|
|
| Amyotrophic Lateral Sclerosis 1 |
|
Amyotrophic Lateral Sclerosis
|
ALS
|
|
Lou Gehrig Disease
|
Amyotrophic Lateral Sclerosis Type 1
|
|
Charcot Disease
|
ALS1
|
|
Amyotrophic Lateral Sclerosis, Susceptibility To
|
Fals
|
|
Lou Gehrig'S Disease
|
Mnd
|
|
Motor Neuron Disease
|
Familial Amyotrophic Lateral Sclerosis
|
|
Amyotrophic Lateral Sclerosis 1, Familial
|
Amyotrophic Lateral Sclerosis 1, Autosomal Dominant
|
|
Motor Neuron Disease, Bulbar
|
Motor Neurone Disease
|
|
Amyotrophic Lateral Sclerosis With Dementia
|
Dementia With Amyotrophic Lateral Sclerosis
|
|
Motor Neuron Disease, Amyotrophic Lateral Sclerosis
|
Sclerosis, Lateral, Amyotrophic
|
|
Sclerosis, Lateral, Amyotrophic, Type 1
|
Amyotrophic Sclerosis
|
|
Als - [Amyotrophic Lateral Sclerosis]
|
Wasting Palsy
|
|
Amyotrophic Paralysis
|
Amyotrophy Lateral Sclerosis
|
|
Wasting Paralysis
|
Spinal Progressive Amyotrophy
|
|
Progressive Atrophic Paralysis
|
|
|
| Neuromuscular Disease |
|
Neuromuscular Diseases
|
Neuromuscular Disorders
|
|
Neuromuscular Disorder
|
|
|
