Colorectal Cancer
|
Liver Cirrhosis, Experimental
|
Hypertension
|
Breast Carcinoma
|
Prostatic Neoplasms
|
Autism
|
Epilepsy
|
Seizures
|
Disease Progression
|
Drug-Induced Liver Injury
|
Nervous System Diseases
|
Rheumatoid Arthritis
|
Status Epilepticus
|
Diabetes Mellitus, Type 2
|
Hepatocellular Carcinoma
|
Drug-Related Side Effects And Adverse Reactions
|
Adenoma
|
Liver Cirrhosis
|
Melanoma
|
Hyperalgesia
|
Colonic Neoplasm
|
Diabetes Mellitus, Experimental
|
Nerve Degeneration
|
Renal Cell Carcinoma
|
Drug Dependence
|
Cholestasis
|
Alzheimer's Disease
|
Bipolar Disorder
|
Mesothelioma, Malignant
|
Hernia, Diaphragmatic
|
Schizophrenia
|
Esophageal Neoplasms
|
Lung Neoplasms
|
Inflammation
|
Neoplasm Metastasis
|
Intellectual Disability
|
Memory Disorders
|
Ataxia
|
Atrial Fibrillation
|
Deafness
|
Cell Transformation, Neoplastic
|
Polycystic Ovary Syndrome
|
Peripheral Neuropathy
|
Parkinson's Disease
|
Osteoarthritis
|
Urinary Bladder Neoplasms
|
Neoplasms
|
Myocardial Ischemia
|
Adenocarcinoma
|
Kidney Disease
|
Glioma
|
Epilepsy, Temporal Lobe
|
Respiratory Hypersensitivity
|
Endometriosis
|
Edema
|
Carcinoma
|
Carcinoma, Squamous Cell Of Head And Neck
|
Myocardial Reperfusion Injury
|
Learning Disorders
|
Myocarditis
|
Dermatitis, Allergic Contact
|
Cardiac Arrhythmia
|
Zellweger Syndrome
|
Stomach Neoplasms
|
Obesity
|
Amphetamine-Related Disorders
|
Ovarian Neoplasms
|
Pain
|
Hearing Loss, Sensorineural
|
Developmental Disabilities
|
Fatty Liver
|
Cocaine Dependence
|
Coronary Artery Disease
|
Disease Models, Animal
|
Epilepsy, Absence
|
Diabetes Mellitus, Type 1
|
Coxsackievirus Infections
|
Squamous Cell Carcinoma
|
Reperfusion Injury
|
Diabetic Cardiomyopathies
|
Cardiac Hypertrophy
|
Cataract
|
Deafness, Autosomal Recessive 1a
|
Long Qt Syndrome
|
Lymphoma, Large B-Cell, Diffuse
|
Autism Spectrum Disorder
|
Mammary Neoplasms, Experimental
|
Sinusitis
|
Bare Lymphocyte Syndrome, Type I
|
Primary Biliary Cirrhosis
|
Skin Neoplasms
|
Cone-Rod Dystrophy 2
|
Acute Kidney Injury
|
Amyotrophic Lateral Sclerosis
|
Anemia
|
Anemia, Sideroblastic
|
Anxiety Disorder
|
Arthritis, Juvenile
|
Asthma
|
Atherosclerosis
|
Azoospermia
|
Bartter Syndrome
|
Bartter Syndrome, Type 4a
|
Bone Diseases
|
Brugada Syndrome
|
Calcinosis
|
Cholestasis, Progressive Familial Intrahepatic 1
|
Cleft Lip
|
Cognitive Impairment
|
Congenital Hyperinsulinism
|
Craniofacial Abnormalities
|
Deafness, Autosomal Dominant 2a
|
Deafness, Autosomal Dominant 3a
|
Dementia
|
Diabetes Mellitus, Permanent Neonatal
|
Diabetic Nephropathy
|
Esophageal Squamous Cell Carcinoma
|
Generalized Epilepsy With Febrile Seizures Plus, Type 2
|
Goiter
|
Head And Neck Neoplasms
|
Hearing Loss
|
Noise-Induced Hearing Loss
|
Heart Diseases
|
Herpesviridae Infections
|
Hyperuricemia
|
Hypoxia, Brain
|
Iminoglycinuria
|
Male Infertility
|
Insulin Resistance
|
Intestinal Neoplasms
|
Intestinal Obstruction
|
Kidney Neoplasms
|
Kyphosis
|
Liver Neoplasms
|
Liver Neoplasms, Experimental
|
Lymphoma, Non-Hodgkin
|
Age-Related Macular Degeneration
|
Mammary Neoplasms, Animal
|
Mental Disorders
|
Metabolism, Inborn Errors
|
Microcephaly
|
Movement Disorder
|
Myocardial Infarction
|
Myopia
|
Myotonia Congenita
|
Neoplasm Invasiveness
|
Neuropathic Pain
|
Neuralgia, Postherpetic
|
Neurotoxicity Syndromes
|
Csnb1c
|
Non-Alcoholic Fatty Liver Disease
|
Osteochondrodysplasias
|
Osteosarcoma
|
Pancreatitis
|
Parkinsonian Disorders
|
Peroxisome Biogenesis Disorders
|
Poisoning
|
Acute Lymphoblastic Leukemia
|
Pruritus
|
Renal Hypouricemia
|
Respiratory Insufficiency
|
Sitosterolemia
|
Substance Withdrawal Syndrome
|
Sudden Infant Death
|
Tachycardia, Ventricular
|
Tooth Abnormalities
|
Torsades De Pointes
|
Dilated Cardiomyopathy
|
Cardiomyopathies
|
Skin Diseases
|
Diarrhea
|
Diastrophic Dysplasia
|
Carcinoma, Non-Small-Cell Lung
|
Carcinoma, Intraductal, Noninfiltrating
|
Disease Susceptibility
|
Down Syndrome
|
Drug Eruptions
|
Drug Hypersensitivity
|
Carcinoma, Ductal
|
Carcinoma, Adenoid Cystic
|
Dyslipidemias
|
Limb Dystonia
|
Ear Diseases
|
Ectodermal Dysplasia
|
Cantu Syndrome
|
Ehlers-Danlos Syndrome
|
Encephaloclastic Proliferative Vasculopathy
|
Endometrial Neoplasm
|
Brugada Syndrome 8
|
End Stage Liver Disease
|
Enterovirus Infections
|
Epilepsies, Myoclonic
|
Brugada Syndrome 3
|
Bronchiectasis With Or Without Elevated Sweat Chloride 1
|
Epilepsy, Benign Neonatal
|
Epilepsy, Generalized
|
Epilepsy, Idiopathic Generalized
|
Bronchial Hyperreactivity
|
Epileptic Encephalopathy, Early Infantile, 1
|
Epileptic Encephalopathy, Early Infantile, 3
|
Epiphyseal Dysplasia, Multiple, 4
|
Episodic Ataxia, Type 1
|
Episodic Ataxia, Type 2
|
Episodic Ataxia, Type 6
|
Erectile Dysfunction
|
Erythrocyte Lactate Transporter Defect
|
Erythrokeratodermia Variabilis
|
Erythromelalgia
|
Escherichia Coli Infections
|
Esophageal Diseases
|
Brain Ischemia
|
Adenocarcinoma, Clear Cell
|
Esophagitis
|
Exfoliation Syndrome
|
Familial Hypophosphatemic Rickets
|
Fanconi Syndrome
|
Brain Diseases
|
Focal Segmental Glomerulosclerosis 2
|
Folate Malabsorption, Hereditary
|
Fractures, Bone
|
Gallbladder Disease 4
|
Gallbladder Neoplasm
|
Gallstones
|
Gastrointestinal Diseases
|
Generalized Epilepsy And Paroxysmal Dyskinesia
|
Generalized Epilepsy With Febrile Seizures Plus, Type 1
|
Sleep Wake Disorders
|
Genetic Predisposition To Disease
|
Gitelman Syndrome
|
Brachyolmia Type 3
|
Iga Glomerulonephritis
|
Membranous Glomerulonephritis
|
Glucose-Galactose Malabsorption
|
Glucose Intolerance
|
Glut1 Deficiency Syndrome
|
Glycogen Storage Disease Ib
|
Glycogen Storage Disease Ic
|
Glycosuria, Renal
|
Soft Tissue Neoplasms
|
Gout
|
Hallermann's Syndrome
|
Harlequin Type Ichthyosis
|
Hartnup Disease
|
Spastic Paraplegia 42, Autosomal Dominant
|
Spastic Paraplegia 44, Autosomal Recessive
|
Spastic Paraplegia 6, Autosomal Dominant
|
Bone Marrow Diseases
|
Heart Block
|
Heartburn
|
Heart Defects, Congenital
|
Speech Disorders
|
Heart Failure
|
Hematologic Neoplasms
|
Hemihyperplasia, Isolated
|
Hemiplegic Migraine, Familial Type 1
|
Hemophagocytic Lymphohistiocytosis, Familial, 2
|
Hepatitis B
|
Hereditary Motor And Sensory Neuropathy, Type Iic
|
Hereditary Pancreatitis
|
Bone Diseases, Metabolic
|
Spermatogenic Failure 7
|
Hidradenitis Suppurativa
|
Hid Syndrome
|
Hiv Infections
|
Hyperaldosteronism
|
Bone Diseases, Developmental
|
Hyperbilirubinemia
|
Hyperexplexia Hereditary
|
Hyperhomocysteinemia
|
Hyperinsulinemic Hypoglycemia, Familial, 7
|
Hyperkeratosis, Epidermolytic
|
Hyperkinesis
|
Hypermanganesemia With Dystonia Polycythemia And Cirrhosis
|
Hyperoxaluria
|
Allergy
|
Bile Acid Malabsorption, Primary
|
Hypertension, Essential
|
Pulmonary Hypertension
|
Hypertrophy
|
Spinal Cord Injuries
|
Familial Hdl Deficiency
|
Hypoglycemia
|
Hypoglycemia, Leucine-Induced
|
Hypokalemic Periodic Paralysis, Type 2
|
Hypomagnesemia 1, Intestinal
|
Hypomyelination, Global Cerebral
|
Hyponatremia
|
Hypoplastic Left Heart Syndrome
|
Hypotension
|
Orthostatic Hypotension
|
Hypouricemia, Renal, 2
|
Spinocerebellar Ataxia 13
|
Ichthyosis
|
Ichthyosis, Lamellar
|
Idiopathic Basal Ganglia Calcification 1
|
Spinocerebellar Ataxia 15
|
Immunologic Deficiency Syndromes
|
Indifference To Pain, Congenital, Autosomal Recessive
|
Infertility
|
Spinocerebellar Ataxia 29
|
Behcet's Syndrome
|
Inflammatory Bowel Disease 13
|
Inflammatory Bowel Disease
|
Influenza, Human
|
Spinocerebellar Ataxias
|
Basal Ganglia Diseases
|
Intervertebral Disc Disease
|
Spondylocheirodysplasia, Ehlers-Danlos Syndrome-Like
|
Spondylometaphyseal Dysplasia, Kozlowski Type
|
Intracranial Hemorrhages
|
Intrahepatic Cholestasis Of Pregnancy
|
Jaundice, Chronic Idiopathic
|
Jaundice, Obstructive
|
Jervell-Lange Nielsen Syndrome
|
Keloid
|
Keratitis
|
Keratitis, Ichthyosis, And Deafness (Kid) Syndrome
|
Keratoderma, Palmoplantar
|
Kidney Stone
|
Bartter Syndrome, Type 4b
|
Kidney Failure, Chronic
|
Stargardt Disease 1
|
Knuckle Pads, Leuconychia And Sensorineural Deafness
|
Acute Lung Injury
|
Lamellar Ichthyosis, Type 2
|
Language Development Disorders
|
Bartter Syndrome, Type 3
|
Leigh Disease
|
Chronic Lymphocytic Leukemia
|
Leukemia, Myeloid, Acute
|
Leukodystrophy, Hypomyelinating, 2
|
Limb Deformities, Congenital
|
Lipid Metabolism, Inborn Errors
|
Lipidoses
|
Bartter Syndrome, Antenatal Type 1
|
Alcoholic Liver Cirrhosis
|
Barrett's Esophagus
|
Attention Deficit Hyperactivity Disorder
|
Acrodermatitis Enteropathica
|
Stroke
|
Atrial Standstill
|
Long Qt Syndrome 2
|
Long Qt Syndrome 3
|
Long Qt Syndrome Type 3
|
Low Molecular Weight Proteinuria With Hypercalciuria And Nephrocalcinosis
|
Atrial Fibrillation, Familial, 7
|
Systemic Lupus Erythematosus
|
Lymphatic Metastasis
|
Lymphoma, Follicular
|
Atrial Fibrillation, Familial, 3
|
Acrodermatitis
|
Vomiting
|
Macular Degeneration, Age-Related, 2
|
Major Affective Disorder 1
|
Malabsorption Syndromes
|
Malignant Hyperthermia
|
Malignant Hyperthermia Susceptibility Type 1
|
Malignant Hyperthermia Susceptibility Type 5
|
Weight Gain
|
Atrial Fibrillation, Familial 1
|
Manganese Poisoning
|
Marijuana Dependence
|
Megacolon
|
Atelosteogenesis Type 2
|
Ataxia With Vitamin E Deficiency
|
Surfactant Metabolism Dysfunction, Pulmonary, 3
|
Mental Retardation, Autosomal Recessive 7
|
Mental Retardation, X-Linked 95
|
Mesothelioma
|
Asperger Syndrome
|
Syndactyly, Type 3
|
Metaplasia
|
Metatropic Dwarfism
|
Systemic Carnitine Deficiency
|
Micronuclei, Chromosome-Defective
|
Migraine, Familial Hemiplegic, 3
|
Minicore Myopathy With External Ophthalmoplegia
|
Mitochondrial Myopathies
|
Mitochondrial Phosphate Carrier Deficiency
|
Mood Disorder
|
Mouth Neoplasms
|
Tachycardia
|
Multiple Myeloma
|
Muscular Atrophy
|
Muscular Atrophy, Spinal
|
Myasthenic Syndromes, Congenital
|
Xanthomatosis
|
Arthritis, Experimental
|
Arterial Tortuosity Syndrome
|
Arrhythmogenic Right Ventricular Dysplasia, Familial, 2
|
Myoclonic Epilepsies, Progressive
|
Myoclonic Epilepsy, Juvenile
|
Myopathies, Structural, Congenital
|
Myopathy, Central Core
|
Temple-Baraitser Syndrome
|
Myotonia
|
Thyroid Dyshormonogenesis 1
|
Myotonic Disorders
|
Nasopharyngeal Carcinoma
|
Nausea
|
Necrosis
|
Neonatal-Onset Citrullinemia Type 2
|
Thyroid Carcinoma
|
Apnea
|
Anoxia
|
Neoplasms, Germ Cell And Embryonal
|
Nephrocalcinosis
|
Nephrolithiasis, X-Linked Recessive, With Renal Failure
|
Nephrotic Syndrome, Idiopathic, Steroid-Resistant
|
Anemia, Sideroblastic Spinocerebellar Ataxia
|
Anemia, Sideroblastic, Pyridoxine-Refractory, Autosomal Recessive
|
Tic Disorders
|
Timothy Syndrome
|
Neuroblastoma
|
Neuromyelitis Optica
|
Tongue Neoplasms
|
Neutropenia
|
Achromatopsia 2
|
Zimmerman Laband Syndrome
|
Anemia, Hemolytic, Autoimmune
|
Obesity, Morbid
|
Obsessive-Compulsive Disorder
|
Oculocutaneous Albinism Type 2
|
Oculodentodigital Dysplasia
|
Oculodentodigital Dysplasia, Autosomal Recessive
|
Oligospermia
|
Neurocirculatory Asthenia
|
Osteitis Deformans
|
Amyloidosis, Familial Visceral
|
Translocation, Genetic
|
Osteopetrosis
|
Osteopetrosis, Autosomal Recessive 4
|
Tremor
|
Amish Lethal Microcephaly
|
Androgenetic Alopecia
|
Pain Insensitivity, Congenital
|
Pain, Postoperative
|
Palmoplantar Keratoderma With Deafness
|
Acidosis
|
Pancreatitis, Chronic
|
Pancytopenia
|
Paralysis
|
Paralysis, Hyperkalemic Periodic
|
Paranoid Disorders
|
Parastremmatic Dwarfism
|
Allan-Herndon-Dudley Syndrome
|
Parkinson Disease, Secondary
|
Urinary Bladder, Overactive
|
Parkinsonism-Dystonia, Infantile
|
Paroxysmal Extreme Pain Disorder
|
Paroxysmal Ventricular Fibrillation
|
Pediatric Obesity
|
Pendred Syndrome
|
Alcohol Dependence
|
Peritoneal Neoplasms
|
Urination Disorders
|
Personality Disorders
|
Pneumonia
|
Urolithiasis
|
Polycystic Kidney, Autosomal Recessive
|
Aland Island Eye Disease
|
Polycythemia
|
Polymorphic Catecholergic Ventricular Tachycardia
|
Posterior Column Ataxia With Retinitis Pigmentosa
|
Potassium Aggravated Myotonia
|
Precancerous Conditions
|
Vascular Diseases
|
Precursor T-Cell Lymphoblastic Leukemia-Lymphoma
|
Prenatal Injuries
|
Progressive External Ophthalmoplegia With Mitochondrial Dna Deletions, Autosomal Dominant, 1
|
Progressive External Ophthalmoplegia With Mitochondrial Dna Deletions, Autosomal Dominant, 2
|
Progressive Familial Heart Block, Type Ib
|
Aids-Related Kaposi Sarcoma
|
Proteinuria
|
Ventricular Dysfunction, Left
|
Pseudoxanthoma Elasticum
|
Psoriasis
|
Psychomotor Disorders
|
Psychoses, Substance-Induced
|
Chronic Obstructive Pulmonary Disease
|
Recurrence
|
Refractive Errors
|
Ventricular Fibrillation
|
Afibrinogenemia
|
Adult-Onset Citrullinemia Type 2
|
Vitamin B 12 Deficiency
|
Retinal Cone Dystrophy 3b
|
Retinal Degeneration
|
Achondrogenesis Type 1b
|
Retinitis Pigmentosa 19
|
Rhabdomyosarcoma 1
|
Rhinitis
|
Romano-Ward Syndrome
|
Salivary Gland Neoplasm
|
Sarcoma, Synovial
|
Adrenoleukodystrophy
|
Adrenocortical Carcinoma
|
Intracerebral Hemorrhage
|
Ceroid Lipofuscinosis, Neuronal, 7
|
Charcot-Marie-Tooth Disease
|
Charcot-Marie-Tooth Disease, X-Linked, 1
|
Cholangiocarcinoma
|
Cholangitis
|
Sclerosing Cholangitis
|
Choledochal Cyst
|
Cerebellar Ataxia
|
Cholestasis, Intrahepatic
|
Febrile Seizures
|
Cholestasis, Benign Recurrent Intrahepatic, 2
|
Cholestasis, Progressive Familial Intrahepatic 3
|
Chondrocalcinosis 2
|
Chondrosarcoma, Mesenchymal
|
Chronic Pain
|
Shock, Hemorrhagic
|
Cellulitis
|
Short Qt Syndrome 1
|
Ulcerative Colitis
|
Cataract, Zonular Pulverulent 3
|
Colonic Polyps
|
Cataract, Zonular Pulverulent 1
|
Cone-Rod Dystrophy 3
|
Cone-Rod Dystrophy, X-Linked, 3
|
Congenital Bilateral Aplasia Of Vas Deferens
|
Short Qt Syndrome 2
|
Connective Tissue Diseases
|
Coronary Aneurysm
|
Cataract Microcornea Syndrome
|
Coronary Heart Disease
|
Cataract, Juvenile, With Microcornea And Glucosuria
|
N-Acetylneuraminic Acid Storage Disease
|
Craniometaphyseal Dysplasia, Autosomal Dominant
|
Cystic Fibrosis
|
Cystinosis
|
Cystinosis, Late-Onset Juvenile Or Adolescent Nephropathic Type
|
Cystinosis, Ocular Nonnephropathic
|
Cataract, Autosomal Dominant
|
Deafness, Autosomal Dominant 25
|
Sick Sinus Syndrome 1, Autosomal Recessive
|
Deafness, Autosomal Dominant 2b
|
Sick Sinus Syndrome 2, Autosomal Dominant
|
Deafness, Autosomal Dominant 3b
|
Cardiovascular Disease
|
Deafness, Autosomal Recessive 1b
|
Death
|
Lung Adenocarcinoma
|
Dent Disease
|
Dent Disease 1
|
Unipolar Depression
|
Major Depression
|
Cardiomyopathy, Hypertrophic
|
Dermatitis, Contact
|
Cardiomyopathy, Familial Hypertrophic, 1
|
Diabetes Insipidus, Nephrogenic
|
Cardiomyopathy, Dilated, 1o
|
Vohwinkel Syndrome
|
Diabetes Mellitus, Transient Neonatal, 2
|
Diabetes Mellitus, Transient Neonatal, 3
|
Cardiomyopathy, Dilated, 1e
|