Liver Cirrhosis, Experimental
|
Hepatocellular Carcinoma
|
Neoplasm Invasiveness
|
Breast Carcinoma
|
Prostatic Neoplasms
|
Mammary Neoplasms, Animal
|
Mammary Neoplasms, Experimental
|
Hypertension
|
Carcinoma
|
Lung Neoplasms
|
Drug-Induced Liver Injury
|
Myocardial Ischemia
|
Cholangiocarcinoma
|
Glioma
|
Diabetes Mellitus, Experimental
|
Adenocarcinoma
|
Cocaine Dependence
|
Autism
|
Osteoarthritis
|
Hemangioma
|
Fibrosis
|
Colorectal Cancer
|
Stomach Neoplasms
|
Neoplasm Metastasis
|
Osteoporosis
|
Amino Acid Metabolism, Inborn Errors
|
Lung Adenocarcinoma
|
Melanoma
|
Ovarian Neoplasms
|
Disease Progression
|
Leukemia, Myeloid, Acute
|
Obesity
|
Carcinoma, Adenoid Cystic
|
Squamous Cell Carcinoma
|
Leukemia
|
Carcinoma, Non-Small-Cell Lung
|
Parkinson's Disease
|
Heart Failure
|
Mouth Neoplasms
|
Colorectal Neoplasms, Hereditary Nonpolyposis
|
Myocardial Reperfusion Injury
|
Neoplasm Recurrence, Local
|
Neoplasms, Experimental
|
Craniofacial Abnormalities
|
Nerve Degeneration
|
Neuroblastoma
|
Kidney Disease
|
Carcinoma, Squamous Cell Of Head And Neck
|
Oligodendroglioma
|
Dermatitis, Contact
|
Anoxia
|
Pancreatic Carcinoma
|
Arthritis, Juvenile
|
Parkinsonian Disorders
|
Leukemia, Promyelocytic, Acute
|
Diabetes Mellitus, Type 2
|
Polycystic Ovary Syndrome
|
Amphetamine-Related Disorders
|
Precancerous Conditions
|
Acute Lymphoblastic Leukemia
|
Liver Diseases
|
Liver Neoplasms
|
Liver Neoplasms, Experimental
|
Asthma
|
Reperfusion Injury
|
Salivary Gland Neoplasm
|
Enchondromatosis
|
Sezary Syndrome
|
Alcohol Dependence
|
Endometrial Neoplasm
|
Testicular Germ Cell Tumor
|
Chondroma
|
Turcot Syndrome
|
Esophageal Neoplasms
|
Fatty Liver
|
Hyperinsulinemic Hypoglycemia, Familial, 3
|
Hypermethioninemia
|
Hyperparathyroidism
|
Hyperparathyroidism, Neonatal Severe Primary
|
Hyperplasia
|
Hypertrophy
|
Left Ventricular Hypertrophy
|
Hyperuricemia
|
Hypocalcemia
|
Hypocalciuric Hypercalcemia, Familial, Type 1
|
Hypoparathyroidism
|
Hypoparathyroidism Familial Isolated
|
Hypotonia-Cystinuria Syndrome
|
Hypoxia-Ischemia, Brain
|
Idiopathic Pulmonary Fibrosis
|
Immunoblastic Lymphadenopathy
|
Male Infertility
|
Insulin Resistance
|
Intellectual Disability
|
Intestinal Polyposis
|
Invasive Pneumococcal Disease, Recurrent Isolated, 1
|
Irak4 Deficiency
|
Juvenile Polyposis Syndrome
|
Korsakoff Syndrome
|
Lameness, Animal
|
Language Development Disorders
|
Leopard Syndrome
|
Lesch-Nyhan Syndrome
|
Chronic Lymphocytic Leukemia
|
Leukemia-Lymphoma, Adult T-Cell
|
Chronic Myelogenous Leukemia
|
Lewy Body Dementia
|
Lipomatosis
|
Long Qt Syndrome
|
Lymphoma
|
Lymphoma, Follicular
|
Lymphoma, T-Cell, Peripheral
|
Colorectal Cancer, Hereditary Nonpolyposis, Type 1
|
Macrocephaly Autism Syndrome
|
Macrophage Activation Syndrome
|
Manganese Poisoning
|
Mason-Type Diabetes
|
Maturity-Onset Diabetes Of The Young, Type 2
|
Megalocytic Interstitial Nephritis
|
Meningioma
|
Meningioma, Familial
|
Mental Disorders
|
Mesothelioma, Malignant
|
Microsatellite Instability
|
Motor Skills Disorders
|
Mouth Diseases
|
Muir-Torre Syndrome
|
Multiple Sclerosis
|
Musculoskeletal Pain
|
Myelodysplastic Syndromes
|
Myocardial Infarction
|
Nasopharyngeal Carcinoma
|
Neoplasms, Glandular And Epithelial
|
Nephroblastomatosis, Fetal Ascites, Macrosomia And Wilms Tumor
|
Neurodegenerative Diseases
|
Neurofibromatosis 1
|
Optic Atrophy 1 And Deafness
|
Optic Atrophy, Autosomal Dominant
|
Optic Atrophy Polyneuropathy Deafness
|
Pain
|
Panic Disorder
|
Parkinson Disease 4, Autosomal Dominant Lewy Body
|
Parkinson Disease 6, Autosomal Recessive Early-Onset
|
Peutz-Jeghers Syndrome
|
Pheochromocytoma
|
Phosphoenolpyruvate Carboxykinase Deficiency
|
Phosphoribosylpyrophosphate Synthetase Superactivity
|
Polydactyly
|
Prostatic Intraepithelial Neoplasia
|
Proteus Syndrome
|
Pseudohypoaldosteronism
|
Psychomotor Disorders
|
Psychoses, Substance-Induced
|
Pyruvate Dehydrogenase Phosphatase Deficiency
|
Pyruvate Kinase Deficiency Of Red Cells
|
Recurrence
|
Cone-Rod Dystrophy 2
|
Schizophrenia
|
Seizures
|
Skin Diseases
|
Small Cell Lung Carcinoma
|
Spinal Cord Injuries
|
Status Epilepticus
|
Substance Withdrawal Syndrome
|
Temporomandibular Joint Disorder
|
Thrombophilia, X-Linked, Due To Factor Ix Defect
|
Thrombosis
|
Thyroid Cancer, Follicular
|
Uridine 5-Prime Monophosphate Hydrolase Deficiency, Hemolytic Anemia Due To
|
Urinary Bladder Neoplasms
|
Vacterl Association With Hydrocephalus
|
Ventricular Dysfunction, Left
|
Weight Gain
|
Werner Syndrome
|
2-Hydroxyglutaricaciduria
|
Wernicke Encephalopathy
|
3-Hydroxy-3-Methylglutaryl-Coa Lyase Deficiency
|
Abnormalities, Multiple
|
Acute Coronary Syndrome
|
Acute Kidney Injury
|
Adenoma, Liver Cell
|
Adenosine Triphosphate, Elevated, Of Erythrocytes
|
Adrenocortical Carcinoma
|
Aging, Premature
|
Alzheimer's Disease
|
Amnesia
|
Anemia, Hemolytic
|
Anemia, Hemolytic, Congenital Nonspherocytic
|
Anisometropia
|
Rheumatoid Arthritis
|
Arts Syndrome
|
Astrocytoma
|
Attention Deficit Hyperactivity Disorder
|
Autoimmune Disease
|
Biliary Tract Neoplasms
|
Bipolar Disorder
|
Bone Diseases, Developmental
|
Brain Diseases
|
Brain Diseases, Metabolic, Inborn
|
Cafe Au Lait Spots, Multiple
|
Carcinogenesis
|
Basal Cell Carcinoma
|
Renal Cell Carcinoma
|
Cardiomyopathies
|
Dilated Cardiomyopathy
|
Cardiomyopathy, Hypertrophic
|
Cell Transformation, Neoplastic
|
Chloracne
|
Cholestasis
|
Cholestasis, Intrahepatic
|
Cholestasis, Progressive Familial Intrahepatic 1
|
Coffin-Lowry Syndrome
|
Cognitive Impairment
|
Ulcerative Colitis
|
Congenital Hyperinsulinism
|
Coronary Vessel Anomalies
|
Coumarin Resistance
|
Deafness, X-Linked 1
|
Demyelinating Diseases
|
Developmental Disabilities
|
Diabetes Mellitus
|
Diabetes Mellitus, Permanent Neonatal
|
Digeorge Syndrome
|
Disease Models, Animal
|
Drug-Related Side Effects And Adverse Reactions
|
Endocrine-Cerebroosteodysplasia
|
Endometrial Hyperplasia
|
Enterocolitis
|
Enterocolitis, Necrotizing
|
Epilepsy
|
Epilepsy, Idiopathic Generalized
|
Epilepsy, Temporal Lobe
|
Fetal Growth Retardation
|
Gamma-Glutamylcysteine Synthetase Deficiency, Hemolytic Anemia Due To
|
Gaucher Disease
|
Glutamine Deficiency, Congenital
|
Glutathione Synthetase Deficiency
|
Glutathione Synthetase Deficiency Of Erythrocytes, Hemolytic Anemia Due To
|
Glycogen Storage Disease Xiii
|
Gout, Hprt-Related
|
Hamartoma Syndrome, Multiple
|
Hemophilia A
|
Hemophilia B
|
Hepatic Encephalopathy
|
Hepatolenticular Degeneration
|
Hereditary Autoinflammatory Diseases
|
Hodgkins Lymphoma
|
Hypercalcemia
|
Hypercalciuria, Absorptive, 2
|
Hyperglycemia
|