Liver Cirrhosis, Experimental
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Epilepsy
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Atrial Fibrillation
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Ataxia
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Hypertension
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Long Qt Syndrome
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Epilepsy, Absence
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Autism
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Hyperalgesia
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Glioma
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Noise-Induced Hearing Loss
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Hernia, Diaphragmatic
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Cardiac Arrhythmia
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Seizures
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Intellectual Disability
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Neuropathic Pain
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Status Epilepticus
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Brugada Syndrome
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Diabetes Mellitus, Type 2
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Ventricular Fibrillation
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Febrile Seizures
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Developmental Disabilities
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Myotonia Congenita
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Adenoma
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Herpesviridae Infections
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Diabetes Mellitus, Experimental
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Colonic Neoplasm
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Nerve Degeneration
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Nervous System Diseases
|
Osteoarthritis
|
Neuralgia, Postherpetic
|
Jervell-Lange Nielsen Syndrome
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Breast Carcinoma
|
Bartter Syndrome
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Generalized Epilepsy With Febrile Seizures Plus, Type 1
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Sudden Infant Death
|
Tachycardia, Ventricular
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Generalized Epilepsy With Febrile Seizures Plus, Type 2
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Epilepsy, Idiopathic Generalized
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Epilepsy, Generalized
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Atrial Fibrillation, Familial, 3
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Bartter Syndrome, Type 4a
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Paralysis, Hyperkalemic Periodic
|
Myoclonic Epilepsy, Juvenile
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Bipolar Disorder
|
Torsades De Pointes
|
Esophageal Squamous Cell Carcinoma
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Exfoliation Syndrome
|
Generalized Epilepsy And Paroxysmal Dyskinesia
|
Genetic Predisposition To Disease
|
Granulomatous Disease, Chronic
|
Granulomatous Disease, Chronic, X-Linked
|
Heart Block
|
Heart Failure
|
Hemiplegic Migraine, Familial Type 1
|
Hiv Infections
|
Hyperaldosteronism
|
Hyperkinesis
|
Hyperphagia
|
Hypoglycemia
|
Hypokalemic Periodic Paralysis, Type 2
|
Immunologic Deficiency Syndromes
|
Indifference To Pain, Congenital, Autosomal Recessive
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Infertility, Female
|
Insulin Resistance
|
Intestinal Neoplasms
|
Jervell And Lange-Nielsen Syndrome 2
|
Keloid
|
Kidney Disease
|
Kidney Failure, Chronic
|
Language Development Disorders
|
Lewy Body Dementia
|
Limb Deformities, Congenital
|
Long Qt Syndrome 10
|
Long Qt Syndrome 2
|
Long Qt Syndrome 3
|
Long Qt Syndrome 5
|
Long Qt Syndrome 6
|
Long Qt Syndrome Type 3
|
Malignant Hyperthermia Susceptibility Type 5
|
Mammary Neoplasms, Animal
|
Migraine, Familial Hemiplegic, 3
|
Movement Disorder
|
Multiple Sclerosis
|
Muscular Atrophy
|
Myasthenic Syndromes, Congenital
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Myocardial Ischemia
|
Myocardial Reperfusion Injury
|
Myoclonic Epilepsies, Progressive
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Myopia
|
Myotonia
|
Myotonic Disorders
|
Nasopharyngeal Carcinoma
|
Neoplasm Metastasis
|
Neoplasms
|
Neuroblastoma
|
Neurodegenerative Diseases
|
Csnb1c
|
Obesity
|
Obesity, Morbid
|
Oligospermia
|
Osteosarcoma
|
Ovarian Cysts
|
Pain
|
Pain Insensitivity, Congenital
|
Parkinson's Disease
|
Paroxysmal Extreme Pain Disorder
|
Paroxysmal Ventricular Fibrillation
|
Peripheral Neuropathy
|
Polycystic Kidney, Autosomal Dominant
|
Potassium Aggravated Myotonia
|
Progressive Familial Heart Block, Type Ib
|
Prostatic Neoplasms
|
Proteinuria
|
Pruritus
|
Reperfusion Injury
|
Respiratory Insufficiency
|
Retinal Cone Dystrophy 3b
|
Retinal Cone Dystrophy 4
|
Retinal Diseases
|
Romano-Ward Syndrome
|
Scott Syndrome
|
Sesame Syndrome
|
Short Qt Syndrome 1
|
Short Qt Syndrome 2
|
Short Qt Syndrome 3
|
Sick Sinus Syndrome 1, Autosomal Recessive
|
Sick Sinus Syndrome 2, Autosomal Dominant
|
Skin Diseases
|
Snowflake Vitreoretinal Degeneration
|
Spermatogenic Failure 7
|
Spinocerebellar Ataxia 13
|
Spinocerebellar Ataxias
|
Ankylosing Spondylitis
|
Stomach Neoplasms
|
Temple-Baraitser Syndrome
|
Timothy Syndrome
|
Tremor
|
Urinary Bladder Neoplasms
|
Vascular Diseases
|
Weight Gain
|
Adenocarcinoma
|
Zimmerman Laband Syndrome
|
Aland Island Eye Disease
|
Andersen Syndrome
|
Arsenic Poisoning
|
Arthritis, Juvenile
|
Astrocytoma
|
Atrial Fibrillation, Familial, 4
|
Atrial Fibrillation, Familial, 7
|
Autism Spectrum Disorder
|
Bartter Syndrome, Antenatal , Type 2
|
Bartter Syndrome, Type 3
|
Bartter Syndrome, Type 4b
|
Bone Diseases, Metabolic
|
Brain Infarction
|
Brugada Syndrome 3
|
Brugada Syndrome 4
|
Brugada Syndrome 5
|
Brugada Syndrome 6
|
Brugada Syndrome 7
|
Brugada Syndrome 8
|
Carcinoma
|
Renal Cell Carcinoma
|
Cardiomyopathy, Dilated, 1e
|
Cell Transformation, Neoplastic
|
Cerebellar Ataxia
|
Chorea
|
Chronic Pain
|
Cocaine Dependence
|
Cone-Rod Dystrophy, X-Linked, 3
|
Congenital Hyperinsulinism
|
Deafness
|
Deafness, Autosomal Dominant 2a
|
Diabetes Mellitus
|
Diabetes Mellitus, Permanent Neonatal
|
Diabetes Mellitus, Transient Neonatal, 3
|
Diabetes Mellitus, Type 1
|
Disease Models, Animal
|
Disease Progression
|
Epilepsies, Myoclonic
|
Epilepsy, Benign Neonatal
|
Epilepsy, Temporal Lobe
|
Epileptic Encephalopathy, Early Infantile, 1
|
Episodic Ataxia, Type 1
|
Episodic Ataxia, Type 2
|
Episodic Ataxia, Type 5
|
Erythromelalgia
|