Liver Cirrhosis, Experimental
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Autism
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Cardiomyopathy, Hypertrophic, Familial
|
Dilated Cardiomyopathy
|
Cardiac Hypertrophy
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Colonic Neoplasm
|
Cardiomyopathies
|
Hypertension
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Cardiomyopathy, Familial Hypertrophic, 1
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Cardiomyopathy, Hypertrophic
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Seizures
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Carcinoma, Non-Small-Cell Lung
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Cocaine Dependence
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Acute Coronary Syndrome
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Prostatic Neoplasms
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Osteoporosis
|
Neoplasm Metastasis
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Myasthenic Syndrome, Congenital, Postsynaptic Slow-Channel
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Esophageal Squamous Cell Carcinoma
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Esophageal Neoplasms
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Breast Carcinoma
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Arthritis, Juvenile
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Brain Edema
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Atrial Fibrillation
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Carcinoma
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Renal Cell Carcinoma
|
Chromosome 3, Monosomy 3p25
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Sudden Cardiac Arrest
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Distal Arthrogryposis Type 2b
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Distal Myopathies
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Endometriosis
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Heart Injuries
|
Keloid
|
Liver Diseases
|
Mammary Neoplasms, Animal
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Mammary Neoplasms, Experimental
|
Marijuana Dependence
|
Movement Disorder
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Muscle Weakness
|
Myasthenic Syndrome, Congenital, Fast-Channel
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Myasthenic Syndrome, Congenital, Type Id
|
Myasthenic Syndromes, Congenital
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Myocardial Infarction
|
Myocardial Ischemia
|
Myocardial Reperfusion Injury
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Myotonia Congenita
|
Neoplasm Invasiveness
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Phencyclidine Abuse
|
Schizophrenia
|
Status Epilepticus
|
Stomach Neoplasms
|
Vascular Diseases
|
Weight Gain
|
Cardiomyopathy, Familial Hypertrophic, 4
|
Cardiomyopathy, Familial Hypertrophic, 8
|
Cardiomyopathy, Familial Hypertrophic, 9
|
Cardiomyopathy, Familial Restrictive, 3
|
Rheumatoid Arthritis
|
Cardiac Arrhythmia
|
Cardiovascular Disease
|
Carney Complex Variant
|
Catalepsy
|
Cataract
|
Adenocarcinoma
|
Thoracic Aortic Aneurysm
|
Cognitive Impairment
|
Ulcerative Colitis
|
Aortic Aneurysm, Familial Thoracic 6
|
Copper-Overload Cirrhosis
|
Coronary Aneurysm
|
Coronary Stenosis
|
Creatine Deficiency, X-Linked
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Chronic Obstructive Pulmonary Disease
|
Dermatitis, Allergic Contact
|
Developmental Disabilities
|
Diabetes Mellitus, Experimental
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Disease Models, Animal
|
Respiratory Distress Syndrome, Newborn
|
Respiratory Insufficiency
|
Dyskinesia, Drug-Induced
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Dystonic Disorders
|
Rippling Muscle Disease, 1
|
Epilepsy, Absence
|
Aortic Aneurysm, Familial Thoracic 4
|
Anaphylaxis
|
Familial Dilated Cardiomyopathy
|
Feeding And Eating Disorders
|
Gastrointestinal Diseases
|
Glaucoma
|
Glioma
|
Gliosis
|
Glomerulonephritis
|
Focal Segmental Glomerulosclerosis
|
Guanidinoacetate Methyltransferase Deficiency
|
Hallermann's Syndrome
|
Heart Defects, Congenital
|
Heart Diseases
|
Heart Failure
|
Salivary Gland Neoplasm
|
Heart Septal Defects, Atrial
|
Heart Valve Diseases
|
Hecht Syndrome
|
Hepatitis, Chronic
|
Hereditary Myopathy With Early Respiratory Failure
|
Hernia, Diaphragmatic
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Hyperalgesia
|
Hypercholesterolemia
|
Hyperexplexia Hereditary
|
Hyperhomocysteinemia
|
Hyperkinesis
|
Allergy
|
Amphetamine-Related Disorders
|
Left Ventricular Hypertrophy
|
Hypokalemic Periodic Paralysis, Type 2
|
Hypoplastic Left Heart Syndrome
|
Hypotension
|
Inclusion Body Myopathy 3, Autosomal Dominant
|
Inflammation
|
Intellectual Disability
|
Ischemia
|
Sarcoglycanopathies
|
Kidney Disease
|
Leukemia, Myeloid, Acute
|
Leukemia, Myelomonocytic, Acute
|
Limb-Girdle Muscular Dystrophy, Type 2b
|
Liver Cirrhosis
|
Amino Acid Metabolism, Inborn Errors
|
Scapuloperoneal Syndrome, Neurogenic, Kaeser Type
|
Long Qt Syndrome 12
|
Long Qt Syndrome 9
|
Lung Neoplasms
|
Malignant Hyperthermia
|
Malignant Hyperthermia Susceptibility Type 1
|
Malignant Hyperthermia Susceptibility Type 5
|
Water Intoxication
|
Systemic Scleroderma
|
Acute Lung Injury
|
Megacolon
|
Megacystis Microcolon Intestinal Hypoperistalsis Syndrome
|
Megalencephalic Leukoencephalopathy With Subcortical Cysts
|
Melanoma, Experimental
|
Mental Retardation, X-Linked
|
Minicore Myopathy With External Ophthalmoplegia
|
Mitochondrial Complex I Deficiency
|
Miyoshi Myopathy
|
Mouth Neoplasms
|
Sick Sinus Syndrome
|
Multiple Pterygium Syndrome
|
Sick Sinus Syndrome 2, Autosomal Dominant
|
Muscular Atrophy
|
Muscular Diseases
|
Muscular Dystrophies, Limb-Girdle
|
Muscular Dystrophy, Emery-Dreifuss
|
Muscular Dystrophy, Limb-Girdle, Type 1a
|
Muscular Dystrophy, Limb-Girdle, Type 1c
|
Muscular Dystrophy, Limb-Girdle, Type 2j
|
Muscular Dystrophy, Oculopharyngeal
|
Skin Neoplasms
|
Alzheimer's Disease
|
Ventricular Dysfunction, Left
|
Visceral Myopathy, Familial
|
Substance Withdrawal Syndrome
|
Syndactyly, Type 3
|
Tachycardia, Ventricular
|
Myopathies, Structural, Congenital
|
Myopathy, Central Core
|
Myopathy, Distal, With Anterior Tibial Onset
|
Myopathy, Early-Onset, With Fatal Cardiomyopathy
|
Myopathy, Myosin Storage
|
Myotilinopathy
|
Myotonia
|
Thyroid Diseases
|
Myotonic Disorders
|
Necrosis
|
Nemaline Myopathy 1
|
Nemaline Myopathy 3
|
Nemaline Myopathy 4
|
Thyroid Carcinoma
|
Alpha-B Crystallinopathy
|
Nephrogenic Fibrosing Dermopathy
|
Nephrosis
|
Neurodegenerative Diseases
|
Oculodentodigital Dysplasia
|
Oculodentodigital Dysplasia, Autosomal Recessive
|
Osteoarthritis
|
Adenoma
|
Ovarian Cysts
|
Paralysis
|
Paralysis, Hyperkalemic Periodic
|
Parkinson's Disease
|
Peripheral Neuropathy
|
Tongue Neoplasms
|
Pneumonia
|
Body Weight
|
Bone Diseases, Developmental
|
Bradycardia
|
Bipolar Disorder
|
Barth Syndrome
|
Bronchial Diseases
|
Brugada Syndrome 8
|
Calcinosis
|
Potassium Aggravated Myotonia
|
Carcinoma, Adenoid Cystic
|
Autism Spectrum Disorder
|
Precancerous Conditions
|
Squamous Cell Carcinoma
|
Atrophy
|
Atrial Septal Defect 4
|
Asbestosis
|
Cardiomyopathy, Dilated, 1aa
|
Cardiomyopathy, Dilated, 1d
|
Cardiomyopathy, Dilated, 1ee
|
Cardiomyopathy, Dilated, 1g
|
Cardiomyopathy, Dilated, 1i
|
Cardiomyopathy, Dilated, 1s
|
Cardiomyopathy, Dilated, 1w
|
Cardiomyopathy, Dilated, 1y
|
Arthrogryposis
|
Cardiomyopathy, Familial Hypertrophic, 14
|
Cardiomyopathy, Familial Hypertrophic, 15
|
Cardiomyopathy, Familial Hypertrophic, 2
|
Cardiomyopathy, Familial Hypertrophic, 3
|