Liver Cirrhosis, Experimental
|
Prostatic Neoplasms
|
Obesity
|
Hepatocellular Carcinoma
|
Insulin Resistance
|
Fatty Liver
|
Drug-Induced Liver Injury
|
Diabetes Mellitus, Experimental
|
Heart Failure
|
Breast Carcinoma
|
Stomach Neoplasms
|
Hypertension
|
Autism
|
Lung Neoplasms
|
Inflammation
|
Atherosclerosis
|
Diabetes Mellitus, Type 2
|
Carcinoma
|
Hypercholesterolemia
|
Non-Alcoholic Fatty Liver Disease
|
Melanoma
|
Myocardial Ischemia
|
Colonic Neoplasm
|
Coronary Artery Disease
|
Alzheimer's Disease
|
Weight Gain
|
Kidney Failure, Chronic
|
Adenocarcinoma
|
Cardiovascular Disease
|
Colorectal Cancer
|
Reperfusion Injury
|
Mammary Neoplasms, Animal
|
Mammary Neoplasms, Experimental
|
Dyslipidemias
|
Rheumatoid Arthritis
|
Hypercholesterolemia, Familial
|
Intellectual Disability
|
Cardiac Hypertrophy
|
Schizophrenia
|
Endometriosis
|
Liver Diseases
|
Coronary Heart Disease
|
Endometrial Neoplasm
|
Hyperlipidemias
|
Disease Progression
|
Lipidoses
|
Polycystic Ovary Syndrome
|
Stroke
|
Squamous Cell Carcinoma
|
Liver Neoplasms
|
Cholestasis
|
Drug-Related Side Effects And Adverse Reactions
|
Disease Models, Animal
|
Proteinuria
|
Osteoarthritis
|
Neoplasms
|
Arthritis, Juvenile
|
Myocardial Infarction
|
Acute Kidney Injury
|
Thyroid Carcinoma
|
Skin Diseases
|
Lipid Metabolism, Inborn Errors
|
Kidney Disease
|
Seizures
|
Cardiomyopathies
|
Hyperalgesia
|
Glucose Intolerance
|
Glioma
|
Q Fever
|
Ovarian Neoplasms
|
Neoplasm Metastasis
|
Arthritis, Experimental
|
Hyperlipoproteinemias
|
Peripheral Neuropathy
|
Respiratory Distress Syndrome, Adult
|
Diabetes Mellitus
|
Fever
|
Pain
|
Amphetamine-Related Disorders
|
Carcinoma, Squamous Cell Of Head And Neck
|
Nerve Degeneration
|
Infertility, Female
|
Pancreatic Carcinoma
|
Anoxia
|
Urinary Bladder Neoplasms
|
Dilated Cardiomyopathy
|
Hypertriglyceridemia
|
Fibrosis
|
Craniofacial Abnormalities
|
Hyperplasia
|
Crohn's Disease
|
Unipolar Depression
|
Hyperglycemia
|
Atrophy
|
Ataxia With Vitamin E Deficiency
|
Marijuana Dependence
|
Muscular Diseases
|
Spinal Dysraphism
|
Skin Neoplasms
|
Abortion, Spontaneous
|
Asthma
|
Systemic Lupus Erythematosus
|
Cognitive Impairment
|
Hernia, Diaphragmatic
|
Myocardial Reperfusion Injury
|
Nervous System Diseases
|
Brain Ischemia
|
Alcoholic Liver Cirrhosis
|
Neurodegenerative Diseases
|
Drug Eruptions
|
Liver Cirrhosis
|
Epilepsy
|
Leukemia
|
Esophageal Neoplasms
|
Carcinoma, Adenoid Cystic
|
Pancreatitis
|
Parkinson's Disease
|
Amyotrophic Lateral Sclerosis 1
|
Renal Cell Carcinoma
|
Stomach Ulcer
|
Precancerous Conditions
|
Neurotoxicity Syndromes
|
Abdominal Obesity Metabolic Syndrome
|
Acute Coronary Syndrome
|
Acute Lung Injury
|
Lung Adenocarcinoma
|
Adenomatous Polyposis Coli
|
Developmental Disabilities
|
Amyotrophic Lateral Sclerosis
|
Asthma, Occupational
|
Autoimmune Disease
|
Barrett's Esophagus
|
Behcet's Syndrome
|
Birth Weight
|
Bone Diseases, Metabolic
|
Brain Injuries
|
Bronchial Hyperreactivity
|
Burkitt Lymphoma
|
Carcinoma, Non-Small-Cell Lung
|
Carcinoma, Transitional Cell
|
Cell Transformation, Neoplastic
|
Cholangiocarcinoma
|
Cocaine Dependence
|
Dermatitis, Allergic Contact
|
Dermatitis, Contact
|
Drug Hypersensitivity
|
Duodenal Ulcer
|
Edema
|
Esophageal Squamous Cell Carcinoma
|
Eye Diseases, Hereditary
|
Membranous Glomerulonephritis
|
Graves Ophthalmopathy
|
Heart Diseases
|
Hepatitis C
|
Hepatomegaly
|
Hydronephrosis
|
Hyperemia
|
Hyperinsulinism
|
Hyperlipoproteinemia Type I
|
Hyperthyroidism
|
Ichthyosiform Erythroderma, Brocq Congenital, Nonbullous Form
|
Ichthyosis, Lamellar
|
Immunologic Deficiency Syndromes
|
Infarction, Middle Cerebral Artery
|
Male Infertility
|
Intestinal Polyps
|
Learning Disorders
|
Leopard Syndrome
|
Lewy Body Dementia
|
Lipodystrophy, Congenital Generalized
|
Liver Neoplasms, Experimental
|
Lung Diseases
|
Lymphoma
|
Lymphoma, T-Cell
|
Age-Related Macular Degeneration
|
Malonic Aciduria
|
Meningioma
|
Metabolic Syndrome X
|
Metabolism, Inborn Errors
|
Methemoglobinemia
|
Mouth Diseases
|
Mouth Neoplasms
|
Muscular Atrophy
|
Myelodysplastic Syndromes
|
Myoclonic Epilepsies, Progressive
|
Narcolepsy
|
Necrosis
|
Neoplasm Invasiveness
|
Niemann-Pick Disease, Type C
|
Osteoporosis
|
Phencyclidine Abuse
|
Polyuria
|
Psoriasis
|
Cone-Rod Dystrophy 2
|
Sezary Syndrome
|
Spasms, Infantile
|
Spastic Paraplegia, Hereditary
|
Splenomegaly
|
Status Epilepticus
|
Drug Dependence
|
Thrombosis
|
Thyroid Cancer, Follicular
|
Long-Chain 3-Hydroxyacyl-Coa Dehydrogenase Deficiency
|
Exostoses, Multiple Hereditary
|
Extravasation Of Diagnostic And Therapeutic Materials
|
Eye Diseases
|
Sleep Deprivation
|
Farber Lipogranulomatosis
|
Choledocholithiasis
|
Fatty Liver, Alcoholic
|
Favism
|
Sclerosing Cholangitis
|
Cholangitis
|
Flushing
|
Focal Cortical Dysplasia Of Taylor
|
Gallstones
|
Gastroesophageal Reflux
|
Gaucher Disease
|
Gaucher Disease, Atypical, Due To Saposin C Deficiency
|
Gaucher Disease, Perinatal Lethal
|
Gaucher Disease, Type Iiic
|
Ghosal Hematodiaphyseal Dysplasia
|
Open-Angle Glaucoma
|
Charcot-Marie-Tooth Disease, Type 4b1
|
Glomerulonephritis
|
Glomerulonephritis, Membranoproliferative
|
Small Cell Lung Carcinoma
|
Chanarin-Dorfman Syndrome
|
Glucosephosphate Dehydrogenase Deficiency
|
Glycogen Storage Disease Of Heart, Lethal Congenital
|
Gonadal Dysgenesis Xx Type Deafness
|
Gout
|
Granulomatous Disease, Chronic
|
Smith-Lemli-Opitz Syndrome
|
Growth Disorders
|
Hamartoma Syndrome, Multiple
|
Head And Neck Neoplasms
|
Hearing Disorders
|
Hearing Loss
|
Hearing Loss, Sensorineural
|
Heartburn
|
Somatosensory Disorders
|
Ceroid Lipofuscinosis, Neuronal, 2
|
Hemangioma
|
Hemangiosarcoma
|
Hematologic Neoplasms
|
Hematuria
|
Hemochromatosis
|
Hemolysis
|
Hemorrhoids
|
Hepatitis
|
Hepatitis, Autoimmune
|
Vitamin D Deficiency
|
Hepatitis, Chronic
|
Hepatolenticular Degeneration
|
Spastic Paraplegia 17
|
Hereditary Breast And Ovarian Cancer Syndrome
|
Cerebral Amyloid Angiopathy
|
Heroin Dependence
|
Hiv Infections
|
Spastic Paraplegia 39, Autosomal Recessive
|
Hydroxyacyl-Coa Dehydrogenase, Type 2, Deficiency
|
Carotid Stenosis
|
Hypercholanemia, Familial
|
Carotid Intimal Medial Thickness 1
|
Hypercholesterolemia, Autosomal Dominant, 3
|
Hypercholesterolemia, Autosomal Recessive
|
Vitamin E Deficiency
|
Carotid Artery Diseases
|
Hyperhomocysteinemia
|
Hyperinsulinemic Hypoglycemia, Familial, 4
|
Hyperinsulinemic Hypoglycemia, Familial, 7
|
Spastic Paraplegia 5a, Autosomal Recessive
|
Hyperlipidemia, Combined, 2
|
Carnitine Palmitoyltransferase Ii Deficiency, Lethal Neonatal
|
Carnitine Palmitoyltransferase Ii Deficiency, Late-Onset
|
Speech Disorders
|
Carnitine Palmitoyltransferase Ii Deficiency, Infantile
|
Hyperlipoproteinemia Type Iii
|
Hyperphagia
|
Carnitine Palmitoyl Transferase 1a Deficiency
|
Hypersensitivity, Immediate
|
Cardiomyopathy, Hypertrophic
|
Hypertension, Essential
|
Pulmonary Hypertension
|
Abetalipoproteinemia
|
Cardiomyopathy, Familial Hypertrophic, 6
|
Hypertrophy
|
Familial Hdl Deficiency
|
Hypobetalipoproteinemia, Familial, 2
|
Hypobetalipoproteinemia, Familial, Apolipoprotein B
|
Hypoglycemia
|
Hypogonadism
|
Hypokinesia
|
Hypolipoproteinemias
|
Hypotrichosis
|
Spinocerebellar Ataxia 17
|
Ichthyosis
|
Ichthyosis Follicularis Atrichia Photophobia Syndrome
|
Splenic Diseases
|
Ichthyosis Prematurity Syndrome
|
Ichthyosis, X-Linked
|
Ige Responsiveness, Atopic
|
Vlcad Deficiency
|
Split-Hand-Foot Malformation 6
|
Cardiofaciocutaneous Syndrome
|
Staphylococcal Infections
|
Carcinoma, Medullary
|
Inflammatory Bowel Disease
|
Carcinoma In Situ
|
Carcinoma, Ductal, Breast
|
Stargardt Disease 3
|
Intrahepatic Cholestasis Of Pregnancy
|
Ischemia
|
Ischemic Attack, Transient
|
Isobutyryl-Coa Dehydrogenase Deficiency
|
Jaundice, Obstructive
|
Joubert Syndrome 1
|
Juvenile Polyposis Syndrome
|
Carcinogenesis
|
Carbohydrate Metabolism, Inborn Errors
|
Kidney Neoplasms
|
Kidney Tubular Necrosis, Acute
|
Krabbe Disease, Atypical, Due To Saposin A Deficiency
|
Language Development Disorders
|
Lathosterolosis
|
Vomiting
|
Lecithin Acyltransferase Deficiency
|
Leiomyosarcoma
|
Lenz Majewski Hyperostotic Dwarfism
|
Toxic Epidermal Necrolysis
|
Cachexia
|
Chronic Lymphocytic Leukemia
|
Leukemia-Lymphoma, Adult T-Cell
|
Leukemia, Myelomonocytic, Juvenile
|
Leukemia, Promyelocytic, Acute
|
Leukodystrophy, Globoid Cell
|
Leukopenia
|
Leukoplakia, Oral
|
Leukostasis
|
46, Xy Disorders Of Sex Development
|
Lipid Metabolism Disorders
|
Burns, Chemical
|
Burns
|
Lipodystrophy
|
3-Hydroxyacyl-Coa Dehydrogenase Deficiency
|
Lipodystrophy, Familial Partial
|
Lipoid Congenital Adrenal Hyperplasia
|
Lipomatosis
|
Lipoprotein Glomerulopathy
|
Liposarcoma
|
Lissencephaly
|
Brucellosis
|
Brain Neoplasms
|
Primary Biliary Cirrhosis
|
Brain Diseases, Metabolic
|
Brain Diseases
|
Liver Diseases, Alcoholic
|
Liver Failure
|
Liver Failure, Acute
|
Brachydactyly With Hypertension
|
3-Hydroxy-3-Methylglutaryl-Coa Synthase 2 Deficiency
|
Long Qt Syndrome
|
2,4-Dienoyl-Coa Reductase Deficiency
|
Lung Injury
|
Bone Neoplasms
|
Blood Platelet Disorders
|
Lymphangioleiomyomatosis
|
Surfactant Metabolism Dysfunction, Pulmonary, 1
|
Lymphoma, B-Cell
|
Lymphoma, Follicular
|
Tachycardia
|
Lymphoma, T-Cell, Cutaneous
|
Lysosomal Acid Lipase Deficiency
|
Macrocephaly Autism Syndrome
|
Tay-Sachs Disease, Ab Variant
|
Macular Degeneration, Age-Related, 1
|
Macular Degeneration, Age-Related, 9
|
Majeed Syndrome
|
Major Affective Disorder 1
|
Major Affective Disorder 7
|
Malaria
|
Testicular Germ Cell Tumor
|
Bile Acid Synthesis Defect, Congenital, 2
|
Autism Spectrum Disorder
|
Atypical Hemolytic Uremic Syndrome
|
Mason-Type Diabetes
|
Maturity-Onset Diabetes Of The Young, Type 1
|
Maturity-Onset Diabetes Of The Young, Type 8, With Exocrine Dysfunction
|
Medium Chain Acyl Coa Dehydrogenase Deficiency
|
Attention Deficit Hyperactivity Disorder
|
Thrombocytopenia
|
Meningioma, Familial
|
Mental Retardation, X-Linked 17
|
Mental Retardation, X-Linked 63
|
Mental Retardation, X-Linked, Syndromic 10
|
Mercury Poisoning
|
Mesothelioma, Malignant
|
Metabolic Diseases
|
Thromboembolism
|
Wolff-Parkinson-White Syndrome
|
Metachondromatosis
|
Metachromatic Leukodystrophy Due To Saposin B Deficiency
|
Woolly Hair, Congenital
|
Methylmalonic Acidemia
|
Mevalonate Kinase Deficiency
|
Morm Syndrome
|
Motor Neuron Disease
|
Motor Skills Disorders
|
3-Hydroxy-3-Methylglutaryl-Coa Lyase Deficiency
|
Tongue Neoplasms
|
Mucositis
|
Multiple Sclerosis
|
Multiple Sclerosis, Relapsing-Remitting
|
Torsades De Pointes
|
Ataxia
|
Zellweger Syndrome
|
Astrocytoma
|
Aspirin Induced Asthma
|
Asthenozoospermia
|
Tuberous Sclerosis
|
Myoglobinuria, Acute Recurrent, Autosomal Recessive
|
Myopathies, Structural, Congenital
|
Myositis
|
Nadh Cytochrome B5 Reductase Deficiency
|
Tuberous Sclerosis 1
|
Nasopharyngeal Carcinoma
|
Nbia2b
|
Urinary Bladder Neck Obstruction
|
2-Methylbutyryl-Coa Dehydrogenase Deficiency
|
Asphyxia Neonatorum
|
Neoplasm Recurrence, Local
|
Arthralgia
|
Neoplastic Processes
|
Neovascularization, Pathologic
|
Nephronophthisis 3
|
Arteritis
|
Arteriosclerosis
|
Neural Tube Defects
|
Neuraminidase 1 Deficiency
|
Neuroblastoma
|
Arsenic Poisoning
|
Neuroectodermal Tumors, Primitive
|
Neurogenic Inflammation
|
Neuronal Ceroid-Lipofuscinoses
|
Neuronopathy, Distal Hereditary Motor, Type V
|
17-Hydroxysteroid Dehydrogenase Deficiency
|
Neutral Lipid Storage Disease With Myopathy
|
Nevus
|
Urination Disorders
|
Niemann-Pick Disease, Type C2
|
Cardiac Arrhythmia
|
Noonan Syndrome
|
Anthracosis
|
Obesity, Abdominal
|
Obesity, Morbid
|
Occupational Diseases
|
Oculocerebrorenal Syndrome
|
Oligospermia
|
Ophthalmoplegia
|
Oral Submucous Fibrosis
|
Oral Ulcer
|
Organophosphate Poisoning
|
Orthomyxoviridae Infections
|
Anorexia
|
Osteoarthropathy, Primary Hypertrophic
|
Osteochondroma
|
Urologic Neoplasms
|
Osteosarcoma
|
Ovarian Cysts
|
Anisometropia
|
Anemia, Hemolytic, Congenital Nonspherocytic
|
Anemia, Hemolytic
|
Anemia
|
Pancreatitis, Chronic
|
Papilloma
|
Paratuberculosis
|
Anaphylaxis
|
Parkinson Disease, Secondary
|
Parkinsonian Disorders
|
Pediatric Obesity
|
Pemphigus
|
Penile Diseases
|
Pericardial Effusion
|
Amyloidosis, Familial Visceral
|
Peroxisomal Acyl-Coa Oxidase Deficiency
|
Peroxisomal Disorders
|
Persian Gulf Syndrome
|
Phagocyte Bactericidal Dysfunction
|
Uveitis
|
Phosphoenolpyruvate Carboxykinase Deficiency
|
Pituitary Acth Hypersecretion
|
Plaque, Atherosclerotic
|
Platelet Glycoprotein Iv Deficiency
|
Polycystic Kidney, Autosomal Dominant
|
Polycystic Kidney, Autosomal Recessive
|
Amyloidosis
|
Polydactyly
|
Polydipsia
|
Polyneuropathies
|
Vacterl Association With Hydrocephalus
|
Porokeratosis, Disseminated Superficial Actinic 1
|
Porphyria Cutanea Tarda
|
Alzheimer Disease Type 2
|
Acute Lymphoblastic Leukemia
|
Premature Birth
|
Prostatic Hyperplasia
|
Prostatic Intraepithelial Neoplasia
|
Alstrom Syndrome
|
Androgenetic Alopecia
|
Proteus Syndrome
|
Pseudovaginal Perineoscrotal Hypospadias
|
Venous Thrombosis
|
Psychoses, Substance-Induced
|
Puberty, Delayed
|
Puberty, Precocious
|
Chronic Obstructive Pulmonary Disease
|
Pulmonary Fibrosis
|
Purpura, Schoenlein-Henoch
|
Leigh Necrotizing Encephalopathy Due To Pyruvate Carboxylase Deficiency
|
Albuminuria
|
Reflex, Abnormal
|
Renal Hepatic Pancreatic Dysplasia Dandy Walker Cyst
|
Renal Insufficiency
|
Agricultural Workers' Diseases
|
Adrenal Insufficiency
|
Retinal Diseases
|
Ventricular Dysfunction, Left
|
Rhizomelic Chondrodysplasia Punctata, Type 3
|
Salivary Gland Neoplasm
|
Adrenal Gland Neoplasms
|
Schnitzler Syndrome
|
Sclerosis
|
Sea-Blue Histiocyte Syndrome
|
Adenoma, Liver Cell
|
Coronary Vasospasm
|
Cortisone Reductase Deficiency
|
Costello Syndrome
|
Constipation
|
Creutzfeldt Jacob Disease
|
Congenital Hemidysplasia With Ichthyosiform Erythroderma And Limb Defects
|
Cyanosis
|
Deafness
|
Death
|
Dent Disease 1
|
Dent Disease 2
|
Combined Saposin Deficiency
|
Dermatitis
|
Dengue Hemorrhagic Fever
|
Atopic Eczema
|
Vision Disorders
|
Desmosterolosis
|
Gestational Diabetes
|
Ulcerative Colitis
|
Colitis
|
Classical Lissencephalies And Subcortical Band Heterotopias
|
Diabetic Cardiomyopathies
|
Diabetic Retinopathy
|
Diarrhea
|
Ciliary Motility Disorders
|
Chronobiology Disorders
|
Disorders Of Sex Development
|
Donnai-Barrow Syndrome
|
Down Syndrome
|
Chromosome Breakage
|
Short Chain Acyl Coa Dehydrogenase Deficiency
|
Chromosome Aberrations
|
Chromosome 2q37 Deletion Syndrome
|
Ductus Arteriosus, Patent
|
Sick Building Syndrome
|
Dysarthria
|
Dysequilibrium Syndrome
|
Chondrodysplasia Punctata 2, X-Linked Dominant
|
Limb Dystonia
|
Adenocarcinoma Of Esophagus
|
Ehlers-Danlos Syndrome Caused By Tenascin-X Deficiency
|
Ehlers-Danlos Syndrome Type 3
|
Emphysema
|
Encephalomyelitis, Autoimmune, Experimental
|
Enchondromatosis
|
Endometrial Hyperplasia
|
Cholesterol Ester Storage Disease
|
Cholestasis, Progressive Familial Intrahepatic 3
|
Endotoxemia
|
End Stage Liver Disease
|
Enterocolitis, Necrotizing
|
Cholestasis, Progressive Familial Intrahepatic 1
|
Epilepsy, Temporal Lobe
|
Erythema
|
Erythrocyte Lactate Transporter Defect
|
Esophageal Diseases
|
Cholelithiasis
|
Abnormalities, Multiple
|
Esophagitis
|
Exanthema
|