Liver Cirrhosis, Experimental
|
Prostatic Neoplasms
|
Breast Carcinoma
|
Hepatocellular Carcinoma
|
Colorectal Cancer
|
Myocardial Ischemia
|
Lung Neoplasms
|
Weight Gain
|
Esophageal Squamous Cell Carcinoma
|
Mammary Neoplasms, Animal
|
Leukemia, Myeloid, Acute
|
Autism
|
Rheumatoid Arthritis
|
Craniofacial Abnormalities
|
Neoplasm Metastasis
|
Melanoma
|
Glioblastoma Multiforme
|
Hypertension
|
Endometriosis
|
Osteoarthritis
|
Neoplasm Invasiveness
|
Carcinoma
|
Mammary Neoplasms, Experimental
|
Thrombosis
|
Liver Neoplasms
|
Carcinoma, Adenoid Cystic
|
Abortion, Spontaneous
|
Drug-Induced Liver Injury
|
Diabetes Mellitus, Type 2
|
Precancerous Conditions
|
Schizophrenia
|
Kidney Disease
|
Disease Models, Animal
|
Salivary Gland Neoplasm
|
Arthritis, Juvenile
|
Stomach Neoplasms
|
Obesity
|
Thromboembolism
|
Keloid
|
Respiratory Distress Syndrome, Adult
|
Nerve Degeneration
|
Colonic Neoplasm
|
Heart Failure
|
Systemic Lupus Erythematosus
|
Myocardial Infarction
|
Astrocytoma
|
Non-Alcoholic Fatty Liver Disease
|
Intellectual Disability
|
Coronary Artery Disease
|
Squamous Cell Carcinoma
|
Mouth Neoplasms
|
Carcinoma, Pancreatic Ductal
|
Liver Cirrhosis
|
Cardiac Hypertrophy
|
Mesothelioma, Malignant
|
Hyperalgesia
|
Atherosclerosis
|
Seizures
|
Esophageal Neoplasms
|
Adenocarcinoma
|
Paratuberculosis
|
Parkinson's Disease
|
Disseminated Intravascular Coagulation
|
Cell Transformation, Neoplastic
|
Status Epilepticus
|
Peripheral Neuropathy
|
Drug Dependence
|
Cocaine Dependence
|
Brain Neoplasms
|
Amphetamine-Related Disorders
|
Alzheimer's Disease
|
Polycystic Ovary Syndrome
|
Dermatitis, Contact
|
Vasospasm, Intracranial
|
Asthma
|
Lung Adenocarcinoma
|
Acute Coronary Syndrome
|
Diabetes Mellitus, Experimental
|
Carcinoma, Non-Small-Cell Lung
|
Renal Cell Carcinoma
|
Osteoporosis
|
Reperfusion Injury
|
Ovarian Neoplasms
|
Hepatolenticular Degeneration
|
Lewy Body Dementia
|
Birth Weight
|
Myocardial Reperfusion Injury
|
Diabetes Mellitus
|
Thyroid Carcinoma
|
Diabetic Retinopathy
|
Calcinosis
|
Unipolar Depression
|
Deafness
|
Autism Spectrum Disorder
|
Diabetes Mellitus, Type 1
|
Thrombophilia
|
Ulcerative Colitis
|
Liver Neoplasms, Experimental
|
Neurodegenerative Diseases
|
Hypercholesterolemia
|
Amyotrophic Lateral Sclerosis 1
|
Mesothelioma
|
Intracerebral Hemorrhage
|
Arthritis, Experimental
|
Pain
|
Cone-Rod Dystrophy 2
|
Disease Progression
|
Cardiovascular Disease
|
Venous Thrombosis
|
Medulloblastoma
|
Vascular Diseases
|
Fatty Liver
|
Acute Kidney Injury
|
Bipolar Disorder
|
Atopic Eczema
|
Allergy
|
Cardiomyopathy, Hypertrophic
|
Urinary Bladder Neoplasms
|
Wounds And Injuries
|
Necrosis
|
Neoplasm Recurrence, Local
|
Eye Abnormalities
|
Coronary Heart Disease
|
Nephritis, Interstitial
|
Facies
|
Alagille Syndrome
|
Neuroectodermal Tumors, Primitive
|
Infection
|
Inflammation
|
Intervertebral Disc Disease
|
Osteochondrodysplasias
|
Ovarian Cysts
|
Pancreatic Carcinoma
|
Pancreatitis
|
Pancreatitis, Chronic
|
Attention Deficit Hyperactivity Disorder
|
Parkinson Disease, Secondary
|
Glioma
|
Deafness, Autosomal Recessive 12
|
Phencyclidine Abuse
|
Growth Disorders
|
Dermatitis
|
Pneumoconiosis
|
Adrenocortical Carcinoma
|
Heart Diseases
|
Polymorphic Catecholergic Ventricular Tachycardia
|
Leukemia, Myelomonocytic, Juvenile
|
Heart Valve Diseases
|
Developmental Disabilities
|
Hematologic Neoplasms
|
Psoriasis
|
Psychosis
|
Chronic Obstructive Pulmonary Disease
|
Purpura, Thrombotic Thrombocytopenic
|
Diabetic Angiopathies
|
Lung Diseases
|
Hemorrhage
|
Diabetic Cardiomyopathies
|
Lymphoma
|
Diabetic Nephropathy
|
Lymphoma, T-Cell, Cutaneous
|
Hepatitis
|
Blood Coagulation Disorders
|
Arteritis
|
Scoliosis
|
Marijuana Dependence
|
Sezary Syndrome
|
Hernia, Diaphragmatic
|
Heterotopia, Periventricular, Autosomal Recessive
|
Bone Diseases
|
Small Cell Lung Carcinoma
|
Spinocerebellar Ataxia 17
|
Splenomegaly
|
Anxiety Disorder
|
Metabolic Diseases
|
Metabolic Syndrome X
|
Syndactyly
|
Limb Dystonia
|
Tachycardia, Ventricular
|
Brain Edema
|
Migraine Without Aura
|
Brain Injuries
|
Hypercholesterolemia, Familial
|
Brain Ischemia
|
Trigeminal Neuralgia
|
Uremia
|
Hyperplasia
|
Usher Syndrome, Type 1d
|
Multiple Sclerosis
|
Uterine Cervical Neoplasms
|
Congenital Abnormalities
|
Van Maldergem Wetzburger Verloes Syndrome
|
Muscular Diseases
|
Asbestosis
|
Epilepsy
|
Venous Thromboembolism
|
Ventricular Dysfunction, Left
|
Left Ventricular Hypertrophy
|
Congenital Hypothyroidism
|
Myelodysplastic Syndromes
|
Hypertension, Essential
|
Pulmonary Hypertension
|
Hyperthyroidism
|
Hypertriglyceridemia
|
Hypertrophy
|
Hypocalcemia
|
Hypocalciuric Hypercalcemia, Familial, Type 1
|
Hypokinesia
|
Hypomagnesemia 4, Renal
|
Hypomyelination, Global Cerebral
|
Hypoparathyroidism
|
Hypoparathyroidism Familial Isolated
|
Hypophosphatemic Rickets, Autosomal Recessive, 1
|
Hypophosphatemic Rickets, Autosomal Recessive, 2
|
Hypoprothrombinemias
|
Hypotrichosis
|
Hypotrichosis And Recurrent Skin Vesicles
|
Hypoxia, Brain
|
Ichthyosis Vulgaris
|
Ige Responsiveness, Atopic
|
Immune Complex Diseases
|
Immune Dysfunction With T-Cell Inactivation Due To Calcium Entry Defect 2
|
Infarction, Middle Cerebral Artery
|
Male Infertility
|
Influenza, Human
|
Intervertebral Disc Degeneration
|
Intracranial Hemorrhages
|
Intracranial Hemorrhage, Traumatic
|
Ischemia
|
Joint Instability
|
Juvenile Macular Degeneration And Hypotrichosis
|
Keratosis Palmoplantaris Striata 1
|
Keutel Syndrome
|
Kidney Diseases, Cystic
|
Kidney Failure, Chronic
|
Kidney Neoplasms
|
Kyphosis
|
Lameness, Animal
|
Language Development Disorders
|
Lassa Fever
|
Learning Disorders
|
Leber Congenital Amaurosis
|
Leigh Disease
|
Leishmaniasis
|
Visceral Leishmaniasis
|
Leukemia
|
Leukemia-Lymphoma, Adult T-Cell
|
Chronic Myelogenous Leukemia
|
Leukemia, Promyelocytic, Acute
|
Leukemia, T-Cell
|
Leukodystrophy, Metachromatic
|
Leukoencephalopathies
|
Limb-Girdle Muscular Dystrophy Type 2a
|
Limb-Girdle Muscular Dystrophy, Type 2b
|
Primary Biliary Cirrhosis
|
Liver Diseases
|
Liver Failure
|
Low Back Pain
|
Lymphangioleiomyomatosis
|
Lymphatic Metastasis
|
Lymphoma, Non-Hodgkin
|
Macular Degeneration, Age-Related, 1
|
Macular Degeneration, Age-Related, 3
|
Macular Degeneration, Age-Related, 4
|
Malaria
|
Malpuech Facial Clefting Syndrome
|
Mandibular Neoplasms
|
Manganese Poisoning
|
Maple Syrup Urine Disease
|
Marfan Syndrome
|
Masp2 Deficiency
|
Mass Syndrome
|
Medullary Cystic Kidney Disease 2
|
Megacolon
|
Megalencephalic Leukoencephalopathy With Subcortical Cysts
|
46,Xy Gonadal Dysgenesis, Complete Or Partial, Dhh-Related
|
Meningitis
|
Mental Retardation, Autosomal Dominant 3
|
Mental Retardation, X-Linked
|
Meretoja Syndrome
|
Mesenteric Ischemia
|
Metabolism, Inborn Errors
|
Metaplasia
|
Methylmalonic Acidemia
|
Micronuclei, Chromosome-Defective
|
Microphthalmia, Isolated, With Coloboma 5
|
Microsatellite Instability
|
Migraine Disorder
|
Mitochondrial Diseases
|
Mitral Valve Prolapse
|
Miyoshi Myopathy
|
Mouth Diseases
|
Movement Disorder
|
Multiple Endocrine Neoplasia
|
Multiple Endocrine Neoplasia Type 2a
|
Multiple Endocrine Neoplasia Type 2b
|
Multiple Myeloma
|
Muscle Hypotonia
|
Muscle Rigidity
|
Muscle Weakness
|
Muscular Dystrophies
|
Muscular Dystrophy, Facioscapulohumeral
|
Muscular Dystrophy, Limb-Girdle, Type 2j
|
Musculoskeletal Pain
|
Mycoplasma Infections
|
Myocardial Stunning
|
Myocarditis
|
Myoclonic Dystonia
|
Myoclonic Epilepsy, Juvenile
|
Myopathy, Distal, With Anterior Tibial Onset
|
Myopathy, Early-Onset, With Fatal Cardiomyopathy
|
Neonatal-Onset Citrullinemia Type 2
|
Neoplasms
|
Neoplasms, Experimental
|
Nephrosis
|
Nephrotic Syndrome
|
Nervous System Diseases
|
Neurobehavioral Manifestations
|
Neuroendocrine Tumors
|
Neuropathy, Painful
|
Neurotoxicity Syndromes
|
Noonan Syndrome
|
No-Reflow Phenomenon
|
Occupational Diseases
|
Ocular Hypertension
|
Oculopalatoskeletal Syndrome
|
Optic Neuritis
|
Oral Submucous Fibrosis
|
Organophosphate Poisoning
|
Ossification Of The Posterior Longitudinal Ligament Of The Spine
|
Osteogenesis Imperfecta
|
Osteosclerosis
|
Paralysis
|
Parkinson Disease 4, Autosomal Dominant Lewy Body
|
Parkinsonian Disorders
|
Pasteurellaceae Infections
|
Pemphigus, Benign Familial
|
Periodontitis
|
Peritoneal Neoplasms
|
Persian Gulf Syndrome
|
Persistent Fetal Circulation Syndrome
|
Pheochromocytoma
|
Pigmentation Disorders
|
Pigmented Paravenous Chorioretinal Atrophy
|
Pitt-Hopkins Syndrome
|
Platelet Disorder, Familial, With Associated Myeloid Malignancy
|
Pleurisy
|
Pneumonia
|
Pneumonia, Pneumococcal
|
Polycystic Kidney, Autosomal Dominant
|
Polycystic Kidney Diseases
|
Polycystic Liver Disease
|
Polyneuropathies
|
Postoperative Complications
|
Precursor B-Cell Lymphoblastic Leukemia-Lymphoma
|
Acute Lymphoblastic Leukemia
|
Precursor T-Cell Lymphoblastic Leukemia-Lymphoma
|
Preeclampsia
|
Premature Birth
|
Prostate Cancer, Familial
|
Prostatic Intraepithelial Neoplasia
|
Protein C Deficiency
|
Pseudoachondroplasia
|
Psychoses, Substance-Induced
|
Pulmonary Embolism
|
Pulmonary Emphysema
|
Pulmonary Fibrosis
|
Purpura Fulminans
|
Purpura, Thrombocytopenic, Idiopathic
|
Pyropoikilocytosis, Hereditary
|
Pyruvate Dehydrogenase Phosphatase Deficiency
|
Q Fever
|
Raine Syndrome
|
Rectum Cancer
|
Recurrence
|
Chronic Kidney Disease
|
Respiratory Hypersensitivity
|
Respiratory Insufficiency
|
Respiratory Tract Infections
|
Retinal Detachment
|
Retinal Diseases
|
Retinal Telangiectasis
|
Retinitis Pigmentosa 12
|
Retinitis Pigmentosa 25
|
Allergic Rhinitis
|
Rigid Spine Syndrome
|
Sagittal Sinus Thrombosis
|
Sarcoglycanopathies
|
Sarcoidosis
|
Sepsis
|
Shprintzen Golberg Craniosynostosis
|
Single Upper Central Incisor
|
Sinus Thrombosis, Intracranial
|
Sjogren Syndrome
|
Skin Diseases
|
Skin Diseases, Vascular
|
Spherocytosis, Type 3
|
Spinal Dysraphism
|
Spondyloepimetaphyseal Dysplasia, Aggrecan Type
|
Spondyloepimetaphyseal Dysplasia, Matrilin-3 Related
|
Spondyloepimetaphyseal Dysplasia, Missouri Type
|
Spondyloepiphyseal Dysplasia, Kimberley Type
|
Toxic Epidermal Necrolysis
|
Stiff Skin Syndrome
|
Stomach Diseases
|
Stomach Ulcer
|
Stroke
|
Substance Withdrawal Syndrome
|
Syndactyly Cenani Lenz Type
|
Synpolydactyly 2
|
Tachycardia
|
Testicular Diseases
|
Testicular Germ Cell Tumor
|
Tetralogy Of Fallot
|
Thrombophilia, X-Linked, Due To Factor Ix Defect
|
Thrombotic Microangiopathies
|
Thyroid Cancer, Medullary
|
Thyroid Cancer, Papillary
|
Thyroid Dyshormonogenesis 2a
|
Thyroid Dyshormonogenesis 6
|
Nicotine Dependence
|
Tooth Abnormalities
|
Hyperostosis-Hyperphosphatemia Syndrome
|
Urticaria
|
Usher Syndromes
|
Usher Syndrome, Type 1f
|
Usher Syndrome, Type 2c
|
Uveal Melanoma
|
Uveitis
|
Varicose Veins
|
Vascular Calcification
|
Vasculitis
|
Vertigo, Benign Recurrent, 2
|
Vestibular Diseases
|
Vitamin D Deficiency
|
Weill-Marchesani Syndrome
|
Wittwer Syndrome
|
Melanoma, Experimental
|
46,Xy Gonadal Dysgenesis, Partial, With Minifascicular Neuropathy
|
Abnormalities, Multiple
|
Acrocapitofemoral Dysplasia
|
Adenocarcinoma Of Esophagus
|
Adenoma, Oxyphilic
|
Adenomatous Polyposis Coli
|
Adult-Onset Citrullinemia Type 2
|
Agricultural Workers' Diseases
|
Alcohol Dependence
|
Alveolar Capillary Dysplasia
|
Ameloblastoma
|
Amelogenesis Imperfecta
|
Amelogenesis Imperfecta, Hypomaturation Type, Iia2
|
Amelogenesis Imperfecta, Hypomaturation Type, Iia1
|
Amino Acid Metabolism, Inborn Errors
|
Amyloidosis, Familial
|
Amyotrophic Lateral Sclerosis
|
Aneurysm
|
Angioedemas, Hereditary
|
Anodontia
|
Anoxia
|
Thoracic Aortic Aneurysm
|
Aortic Rupture
|
Aortic Valve, Calcification Of
|
Aortic Valve Insufficiency
|
Arachnodactyly
|
Arrhythmogenic Right Ventricular Dysplasia, Familial, 10
|
Arrhythmogenic Right Ventricular Dysplasia, Familial, 11
|
Arrhythmogenic Right Ventricular Dysplasia, Familial, 2
|
Arsenic Poisoning
|
Arterial Calcification Of Infancy
|
Arthritis
|
Asthma, Occupational
|
Atrial Fibrillation
|
Atrial Septal Defect 6
|
Atrioventricular Septal Defect, Partial, With Heterotaxy Syndrome
|
Attention Deficit And Disruptive Behavior Disorders
|
Atypical Hemolytic Uremic Syndrome
|
Autoimmune Disease
|
Barrett's Esophagus
|
Basal Ganglia Diseases
|
Blood Platelet Disorders
|
Body Weight
|
Bone Diseases, Metabolic
|
Brachydactyly Type A1
|
Brachyolmia
|
Brain Diseases
|
Brody Myopathy
|
Burkitt Lymphoma
|
Cachexia
|
Cadasil
|
Carbamoyl-Phosphate Synthase I Deficiency Disease
|
Carcinogenesis
|
Carcinoma, Ductal, Breast
|
Carcinoma, Lobular
|
Carcinoma, Medullary
|
Carcinoma, Squamous Cell Of Head And Neck
|
Cardiofaciocutaneous Syndrome
|
Dilated Cardiomyopathy
|
Cardiomyopathy, Dilated, 1aa
|
Cardiomyopathy, Dilated, 1bb
|
Cardiomyopathy, Dilated, 1g
|
Cardiomyopathy, Dilated, 1z
|
Cardiomyopathy, Familial Hypertrophic, 1
|
Cardiomyopathy, Familial Hypertrophic, 10
|
Cardiomyopathy, Familial Hypertrophic, 13
|
Cardiomyopathy, Familial Hypertrophic, 8
|
Cardiomyopathy, Familial Hypertrophic, 9
|
Cardiomyopathy, Hypertrophic, Familial
|
Carnevale Syndrome
|
Celiac Disease
|
Cerebral Infarction
|
Cochlear Diseases
|
Cognitive Impairment
|
Coloboma
|
Coma
|
Cone Dystrophy 3
|
Cone-Rod Dystrophy 5
|
Congenital Central Hypoventilation Syndrome
|
Congenital Contractural Arachnodactyly
|
Congenital Myasthenic Syndrome Ib
|
Congenital Thrombotic Disease, Due To Protein C Deficiency
|
Constipation
|
Corneal Opacity
|
Coronary Restenosis
|
Coronary Vasospasm
|
Costello Syndrome
|
Coumarin Resistance
|
Craniopharyngioma
|
Craniosynostoses
|
Crohn's Disease
|
Cryptorchidism
|
Cutis Laxa, Recessive
|
Cutis Laxa With Severe Pulmonary, Gastrointestinal, And Urinary Abnormalities
|
Darier Disease
|
Deafness, Autosomal Dominant 39, With Dentinogenesis Imperfecta 1
|
Deafness, Autosomal Recessive 23
|
Deafness, Autosomal Recessive 9
|
Dentinogenesis Imperfecta
|
Dentinogenesis Imperfecta, Shields Type 3
|
Dermatitis, Allergic Contact
|
Dermatitis, Atopic, 1
|
Dermatitis, Atopic, 2
|
Desbuquois Syndrome
|
Gestational Diabetes
|
Distal Myopathies
|
Donnai-Barrow Syndrome
|
Down Syndrome
|
Doyne Honeycomb Retinal Dystrophy
|
Drug Hypersensitivity
|
Drug-Related Side Effects And Adverse Reactions
|
Duodenal Ulcer
|
Dysequilibrium Syndrome
|
Dyskinesia, Drug-Induced
|
Dyslipidemias
|
Dyssegmental Dysplasia
|
Dystonia, Dopa-Responsive
|
Ectodermal Dysplasia, Ectrodactyly, And Macular Dystrophy
|
Ectopia Lentis
|
Eczema
|
Elliptocytosis 2
|
Emphysema
|
Encephalomyelitis, Autoimmune, Experimental
|
Endometrial Hyperplasia
|
Endometrial Neoplasm
|
Endotoxemia
|
Eosinophilic Esophagitis
|
Epidermolysis Bullosa Dystrophica
|
Epilepsy, Absence
|
Epilepsy, Female-Restricted, With Mental Retardation
|
Epilepsy, Idiopathic Generalized
|
Epilepsy, Temporal Lobe
|
Epiphyseal Dysplasia, Multiple, 1
|
Epiphyseal Dysplasia, Multiple, 5
|
Erythema Multiforme
|
Eye Diseases, Hereditary
|
Factor Vii Deficiency
|
Factor X Deficiency
|
Factor Xii Deficiency
|
Familial Dilated Cardiomyopathy
|
Familial Medullary Thyroid Carcinoma
|
Febrile Convulsions, Familial, 4
|
Fetal Growth Retardation
|
Fibrosis
|
Fractures, Bone
|
Gaucher Disease
|
Genetic Predisposition To Disease
|
Glaucoma
|
Glaucoma 3, Primary Congenital, D
|
Glaucoma, Angle-Closure
|
Glomerulocystic Kidney Disease With Hyperuricemia And Isosthenuria
|
Iga Glomerulonephritis
|
Glomerulonephritis, Membranoproliferative
|
Focal Segmental Glomerulosclerosis
|
Goiter
|
Griscelli Syndrome Type 1
|
Hajdu-Cheney Syndrome
|
Hashimoto Disease
|
Head And Neck Neoplasms
|
Hearing Loss, Sensorineural
|
Heart Defects, Congenital
|
Heart Injuries
|
Helicobacter Infections
|
Hemangiosarcoma
|
Hematoma
|
Hematoma, Subdural, Acute
|
Hematuria
|
Hemophagocytic Lymphohistiocytosis, Familial, 2
|
Hemophilia A
|
Hemophilia B
|
Hemorrhagic Disorders
|
Hemorrhoids
|
Hennekam Lymphangiectasia Lymphedema Syndrome
|
Hepatitis, Autoimmune
|
Hereditary Angioedema Type Iii
|
Hereditary Angioedema Types I And Ii
|
Hereditary Myopathy With Early Respiratory Failure
|
Hereditary Pancreatitis
|
Hereditary Renal Agenesis
|
Heterotaxy Syndrome
|
Hirschsprung Disease
|
Histiocytoma, Benign Fibrous
|
Hiv Infections
|
Cyclopia
|
Holoprosencephaly 3
|
Hyaloideoretinal Degeneration Of Wagner
|
Hydrops Fetalis
|
Hyperammonemia
|
Hypercalcemia
|
Hyperglycemia
|
Hyperhomocysteinemia
|
Hyperinsulinism
|
Hyperlipidemias
|
Hyperlipoproteinemias
|
Hyperparathyroidism
|
Hyperparathyroidism, Neonatal Severe Primary
|
Hyperparathyroidism, Secondary
|
Hyperphenylalaninemia, Bh4-Deficient, B
|
Hyperphosphatemia
|