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Biological Process
Steroid Metabolic Process
Diseases Associated With Steroid Metabolic Process
Disease
Prostatic Neoplasms
Liver Cirrhosis, Experimental
Hepatocellular Carcinoma
Obesity
Drug-Induced Liver Injury
Fatty Liver
Endometrial Neoplasm
Stomach Neoplasms
Lung Neoplasms
Insulin Resistance
Adenocarcinoma
Breast Carcinoma
Polycystic Ovary Syndrome
Diabetes Mellitus, Experimental
Kidney Failure, Chronic
Cardiac Hypertrophy
Drug-Related Side Effects And Adverse Reactions
Alzheimer's Disease
Dermatitis, Contact
Liver Diseases
Endometriosis
Hypercholesterolemia
Weight Gain
Non-Alcoholic Fatty Liver Disease
Colorectal Cancer
Acute Kidney Injury
Cholestasis
Drug Eruptions
Coronary Artery Disease
Hypertension
Neoplasm Invasiveness
Squamous Cell Carcinoma
Autism
Neoplasms, Hormone-Dependent
Disorders Of Sex Development
Q Fever
Bradycardia
Cell Transformation, Neoplastic
Acute Lymphoblastic Leukemia
Melanoma
Fever
Ataxia With Vitamin E Deficiency
Atherosclerosis
Liver Cirrhosis
Stroke
Coronary Heart Disease
Thrombosis
Liver Neoplasms, Experimental
Lung Injury
Urologic Neoplasms
Glucose Intolerance
Coumarin Resistance
Amphetamine-Related Disorders
Methemoglobinemia
Carcinoma, Non-Small-Cell Lung
Micronuclei, Chromosome-Defective
Carcinoma, Small Cell
Dermatitis, Allergic Contact
Myocardial Ischemia
Hepatitis C
Hepatomegaly
Adrenal Hyperplasia, Congenital
Nephritis, Interstitial
Nervous System Diseases
Cardiomyopathies
Disease Progression
Cardiovascular Disease
Occupational Diseases
Hyperlipidemias
Hypercholesterolemia, Familial
Osteoarthritis
Osteosarcoma
Rheumatoid Arthritis
Parkinson's Disease
Behcet's Syndrome
Dyslipidemias
Androgenetic Alopecia
Chromosome Aberrations
Cocaine Dependence
Cognitive Impairment
Esophageal Neoplasms
Esophageal Squamous Cell Carcinoma
Infertility, Female
Male Infertility
Inflammation
Intellectual Disability
Chronic Obstructive Pulmonary Disease
Colonic Neoplasm
Kidney Disease
Seizures
Sexual Dysfunctions, Psychological
Hypercholesterolemia, Autosomal Dominant, 3
Hypercholesterolemia, Autosomal Recessive
Hyperglycemia
Hyperkalemia
Hyperoxia
Hyperplasia
Allergy
Hypertension, Essential
Hypertension, Malignant
Hypertriglyceridemia
Familial Hdl Deficiency
Hypobetalipoproteinemia, Familial, Apolipoprotein B
Hypogonadism
Hypophosphatemia
Hypopituitarism
Hypotension
Ichthyosis, X-Linked
Jaundice, Neonatal
Kernicterus
Kidney Neoplasms
Lathosterolosis
Lecithin Acyltransferase Deficiency
Lipid Metabolism, Inborn Errors
Lipoid Congenital Adrenal Hyperplasia
Alcoholic Liver Cirrhosis
Liver Diseases, Parasitic
Liver Neoplasms
Long Qt Syndrome
Lymphoma, Non-Hodgkin
Mammary Neoplasms, Animal
Mammary Neoplasms, Experimental
Manganese Poisoning
Marijuana Dependence
Mesothelioma, Malignant
Metabolic Syndrome X
Mevalonate Kinase Deficiency
Mouth Neoplasms
Movement Disorder
Muscle Rigidity
Muscular Diseases
Nadh Cytochrome B5 Reductase Deficiency
Nasopharyngeal Neoplasm
Necrosis
Neoplasms
Neoplastic Processes
Neuropathic Pain
Neural Tube Defects
Neurotoxicity Syndromes
Neutropenia
Niemann-Pick Disease, Type C
Niemann-Pick Disease, Type C2
Obesity, Abdominal
Oligomenorrhea
Ophthalmoplegia
Opisthorchiasis
Ovarian Cysts
Ovarian Neoplasms
Pain
Paranoid Disorders
Pediatric Obesity
Peptic Ulcer Hemorrhage
Peripheral Vascular Diseases
Peters Anomaly
Phencyclidine Abuse
Pituitary Apoplexy
Porokeratosis, Disseminated Superficial Actinic 1
Porphyria Cutanea Tarda
Prenatal Exposure Delayed Effects
Primary Ovarian Insufficiency
Prostatic Hyperplasia
Prostatic Neoplasms, Castration-Resistant
Pseudovaginal Perineoscrotal Hypospadias
Psychomotor Disorders
Puberty, Delayed
Pulmonary Emphysema
Reperfusion Injury
Retinitis
Rhabdomyolysis
Smith-Lemli-Opitz Syndrome
Spasms, Infantile
Spastic Paraplegia, Hereditary
Spastic Paraplegia 5a, Autosomal Recessive
Splenic Diseases
Splenomegaly
Status Epilepticus
Stereotypic Movement Disorder
Drug Dependence
Substance Withdrawal Syndrome
Tachycardia, Sinus
Nicotine Dependence
Torsades De Pointes
Tremor
Urinary Bladder Neoplasms
3-Hydroxy-3-Methylglutaryl-Coa Synthase 2 Deficiency
Weight Loss
46, Xy Disorders Of Sex Development
Abdominal Obesity Metabolic Syndrome
Abetalipoproteinemia
Abortion, Spontaneous
Acth Deficiency, Isolated
Acute Lung Injury
Lung Adenocarcinoma
Adenoma
Adrenal Hyperplasia, Congenital, Type 5
Adrenal Insufficiency
Alcohol Dependence
Amenorrhea
Amyloidosis, Familial Visceral
Amyotrophic Lateral Sclerosis 1
Anorexia
Anoxia
Anxiety Disorder
Arteritis
Arthralgia
Arthritis, Juvenile
Ataxia
Atrophy
Attention Deficit Hyperactivity Disorder
Autism Spectrum Disorder
Autoimmune Disease
Barrett's Esophagus
Basal Ganglia Diseases
Bile Acid Synthesis Defect, Congenital, 2
Bipolar Disorder
Bone Diseases, Metabolic
Brain Diseases
Brain Neoplasms
Brucellosis
Carcinoma
Carcinoma, Large Cell
Carcinoma, Squamous Cell Of Head And Neck
Chest Pain
Chondrodysplasia Punctata 2, X-Linked Dominant
Chromosome 2q37 Deletion Syndrome
Coma
Congenital Adrenal Hyperplasia Due To 11-Beta-Hydroxylase Deficiency
Congenital Adrenal Hyperplasia Due To 21 Hydroxylase Deficiency
Congenital Hemidysplasia With Ichthyosiform Erythroderma And Limb Defects
Cortisone Reductase Deficiency
Craniofacial Abnormalities
Crigler-Najjar Syndrome
Crigler Najjar Syndrome, Type 2
Cushing Syndrome
Cyanosis
Death
Unipolar Depression
Desmosterolosis
Diabetes Mellitus
Diabetes Mellitus, Type 2
Diabetic Cardiomyopathies
Drug Hypersensitivity
Drug Metabolism, Poor, Cyp2c19-Related
Drug Metabolism, Poor, Cyp2d6-Related
Dysarthria
Dysequilibrium Syndrome
Limb Dystonia
Edema
End Stage Liver Disease
Epilepsy, Tonic-Clonic
Exanthema
Fatty Liver, Alcoholic
Gallstones
Gilbert Disease
Glaucoma 1, Open Angle, A
Glaucoma 3, Primary Congenital, A
Glaucoma, Primary Open Angle
Gliosarcoma
Membranous Glomerulonephritis
Glucocorticoid-Remediable Aldosteronism
Glycogen Storage Disease Ib
Glycogen Storage Disease Ic
Glycogen Storage Disease Type I
Graft Vs Host Disease
Growth Disorders
Hamartoma
Hemochromatosis
Hemorrhage
Hepatic Encephalopathy
Hepatitis B
Hepatorenal Form Of Glycogen Storage Disease
Hiv Infections
Hodgkins Lymphoma
Hyperaldosteronism
Hyperbilirubinemia
Hyperbilirubinemia, Transient Familial Neonatal
Related Genes
AKR1C3
AKR1C4
CYP17A1
CYP1A1
CYP1B1
CYP21A2
CYP2A6
CYP2B6
CYP2C19
CYP2C8
CYP2C9
CYP2D6
CYP2E1
CYP3A4
CYP3A5
CYP3A7
HSD17B6
MSMO1
NR1I2
PXR
STARD3
SULT1A1
SULT1A2
SULT2A1
SULT2B1
SULT4A1
TSPO
UGT1A1
UGT1A8
UGT2B15
UGT2B17
UGT2B7
WWOX
