Prediabetes

About the Disease
Prediabetes Syndrome, also known as prediabetes, is related to glucose intolerance and type 1 diabetes mellitus. An important gene associated with Prediabetes Syndrome is INS (Insulin), and among its related pathways/superpathways are Signal Transduction and PI3K-Akt signaling pathway. The drugs Curcumin and Orlistat have been mentioned in the context of this disorder. Affiliated tissues include ovary, heart and kidney, and related phenotypes are no effect and no effect

Common Targets
LPL | FFAR1 | PTGER3 | BRD4 | BRD2 | PPARG | GCK | MAPK11 | CDKAL1 | DPP4 | IAPP | G3630 | Amylin receptor | PIKFYVE | VDR | NOS3 | BDNF-AS | GPR84 | PDE5A | BRD3 | GAA | APOA1 | GLP1R | ATF6 | IDE | Voltage-Gated Calcium Channel alpha-2/delta (nonspecified subtype) | MBOAT4 | TCF7L2 | UCP2 | AMP-activated protein kinase (AMPK) | KCNJ11 | FFAR4

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Other Diseases

Intracranial Hypertension | Charcot-Marie-Tooth Disease Axonal Type 2N | Benign Recurrent Intrahepatic Cholestasis 1 | Diastrophic Dysplasia | Learning Disability | Acute Generalized Exanthematous Pustulosis | Insulinoma | HELLP Syndrome | Atrioventricular Septal Defect | Arthritis, Reactive | Takayasu's Arteritis | Lipid Storage Diseases | Necrotizing Autoimmune Myopathy | Schistosomiasis Mansoni | Cardiofaciocutaneous Syndrome | Coloboma | Thin Basement Membrane Disease | Glycogen Storage Disease Type 5 | Carcinoid Syndrome | Epidermolysis Bullosa Simplex, Localized | 5-oxoprolinase Deficiency | Hepatic Adenomatosis | Cancer, Bladder | Neural Tube Defect | Ureteropelvic Junction Obstruction | Hepatitis, Alcoholic | Pulmonary Capillary Hemangiomatosis | Obesity, Morbid | X-linked Creatine Transporter Deficiency | Osmotic Demyelination Syndrome | Keratoconjunctivitis | Chronic Idiopathic Myelofibrosis | Incontinentia Pigmenti | Hypoplastic Left Heart Syndrome | Presbyopia | Von Hippel-Lindau Disease | Paternal Uniparental Disomy Of Chromosome 14 | Granular Corneal Dystrophy Type 1 | Astrocytoma | Snyder-Robinson Syndrome | Cryptosporidiosis | Renal Oncocytoma | Aldosterone Deficiency | Plasma Cell Leukemia | Non-epidermolytic Palmoplantar Keratoderma | Autosomal Recessive Spastic Paraplegia Type 54 | B-cell Chronic Lymphocytic Leukemia | Photosensitivity | Neutropenia | Platyspondylic Lethal Skeletal Dysplasia, Torrance Type | Persistent Fetal Circulation | Ameloblastoma | Emery-Dreifuss Muscular Dystrophy | Long QT Syndrome Type 2 | Peeling Skin Syndrome, Acral Type | Intestinal Hypomagnesemia 1 | Fibrosis | Christianson Syndrome | Myotonia | Sleep Disorder | Budd-Chiari Syndrome | Primary Sclerosing Cholangitis | Lactose Intolerance | Megacystis-microcolon-intestinal Hypoperistalsis Syndrome | Feingold Syndrome | Bronchitis | Hemochromatosis Type 2 | Cramp Fasciculation Syndrome | Pleomorphic Xanthoastrocytoma | Proteus Syndrome | Hypersensitivity | Atopy | Calcium Pyrophosphate Deposition Disease | Moyamoya Disease | Focal Facial Dermal Dysplasia | Influenza | Parkinson Disease 6, Autosomal Recessive Early-onset | Sialidosis | Carcinoid Tumor | Primrose Syndrome | Ellis-Van Creveld Syndrome | Chorea | Multiple System Atrophy | Hypophosphatemic Rickets, Autosomal Recessive, 1 | Autoimmune Polyendocrine Syndrome | Gestational Trophoblastic Disease | 3-hydroxyacyl-CoA Dehydrogenase Deficiency | Hepatoblastoma | Schnyder Crystalline Corneal Dystrophy | Extramammary Paget's Disease | Campomelic Dysplasia | Cranial Nerve Disease | Scleritis | Pontocerebellar Hypoplasia Type 2 | Fibrodysplasia Ossificans Progressiva | Tetraplegia | Peters-plus Syndrome | Pneumoconiosis | Primary Torsion Dystonia | Gliosarcoma | Hemophilia | Charcot-Marie-Tooth Disease | Richter's Syndrome | Cardiomyopathy, Dilated, 1L | Fibrillation, Atrial | Stroke, Ischemic | Heroin Dependence | Motion Sickness | Polycystic Kidney, Autosomal Recessive | Galactosemia | Microphthalmia | Acrodermatitis | Varices | Familial Advanced Sleep Phase Syndrome | Crimean-Congo Hemorrhagic Fever | Glycogen Storage Disease | Palmoplantar Keratoderma | Anthrax | VACTERL Association | Common Cold | Obsessive-compulsive Disorder | Progressive Familial Intrahepatic Cholestasis Type 1 | Speech Disorders | Congenital Poikiloderma | Autoimmune Interstitial Lung, Joint, And Kidney Disease | Chitayat Syndrome | Hereditary Elliptocytosis | Danon Disease | Neurogenic Bladder | Lysosomal Acid Lipase Deficiency | Anuria | Primary Progressive Nonfluent Aphasia | Pemphigoid | Autosomal Recessive Spastic Paraplegia Type 75 | Burn-McKeown Syndrome | Spinocerebellar Ataxia Type 15 | Neuromyotonia | AIDS | Dupuytren Disease | Lymphedema | Asperger Syndrome | Lymphangioma | Anxiety Disorders | Optic Neuritis | McCune-Albright Syndrome | Rotor Syndrome | Brugada Syndrome 1 | Esotropia | Fibronectin Glomerulopathy | Rosacea | Myelitis | Skin Fragility-woolly Hair Syndrome | Peyronie's Disease | Scleroderma | Desmosterolosis | Osteonecrosis Of The Jaw | Pseudoachondroplasia | Pontocerebellar Hypoplasia Type 7 | Zygomycosis | Shprintzen-Goldberg Syndrome | Peutz-Jeghers Syndrome | Asthma | Delirium | Tonsillitis | Glycogen Storage Disease Type 0 | Familial Glucocorticoid Deficiency | Pyruvate Decarboxylase Deficiency | Primary Aldosteronism | Spinocerebellar Ataxia Type 42 | Cryptococcal Meningitis | Cantu Syndrome | Hemorrhagic Disorders | Huntington's Disease | Hemorrhage | Sengers Syndrome | Asthma, Exercise-induced | Hyperbilirubinemia, Neonatal | Asthma, Nocturnal | Focal Cortical Dysplasia Type 2 | Pycnodysostosis | Meconium Ileus | Gitelman Syndrome | Erectile Dysfunction | Priapism | Amebiasis | Diabetes Insipidus, Nephrogenic | Cardiomyopathy, Peripartum | Fragile X Syndrome | Gerodermia Osteodysplastica | Congenital Sodium Diarrhea | L-2-Hydroxyglutaric Aciduria | Hypotension, Orthostatic | Disseminated Intravascular Coagulation | Exotropia | Uremic Pruritus | Pupil Disorders | Mitochondrial DNA Depletion Syndrome | Familial Hypobetalipoproteinemia | Hypotrichosis Simplex | Mucormycosis | Mountain Sickness | Lymphedema-distichiasis Syndrome | Trigonocephaly | Cancer, Prostate | Lipid Metabolism Disorders | Hypobetalipoproteinemias | Menkes Disease | Congenital Mirror Movements | Hypoalbuminemia | Inflammatory Joint Disease | Cat Eye Syndrome | Borjeson-Forssman-Lehmann Syndrome | Wieacker-Wolff Syndrome | Primary Lateral Sclerosis | Maple Syrup Urine Disease | Encephalopathy, Hepatic | Nijmegen Breakage Syndrome | Chronic Granulomatous Disease | Giant Cell Glioblastoma | Nephritis, Interstitial | Hydrolethalus Syndrome | Chromosome 8q21.11 Deletion Syndrome | Dengue Hemorrhagic Fever | Waldenstrom Macroglobulinemia | Hartsfield Syndrome | Silver-Russell Syndrome | Liddle Syndrome | Congenital Myasthenic Syndrome | Antisocial Personality Disorder | Ghosal Syndrome | Pseudo-pseudohypoparathyroidism | Cold-induced Sweating Syndrome | Acquired Partial Lipodystrophy | Goldenhar Syndrome | Fuchs Dystrophy | Very Long-chain Acyl-CoA Dehydrogenase Deficiency | Thymoma, Malignant | Dent Disease | Spinocerebellar Ataxia Type 7 | Chronic Granulomatous Disease, X-linked | Hypohidrotic Ectodermal Dysplasia | Dyggve-Melchior-Clausen Disease | Anorchia | Adenosine Deaminase 2 Deficiency | Gardner Syndrome | Retinitis | Hydronephrosis | Chromosome 9q34.3 Deletion Syndrome | Histiocytosis | Congenital Hereditary Endothelial Dystrophy Type II | Presbycusis | Antisynthetase Syndrome | Thalassemia | Niemann-Pick Disease, Type A | Vasculitis | Atelosteogenesis Type 2 | Diarrhea | Dermatomyositis | Hereditary Folate Malabsorption | Lesch-Nyhan Syndrome | Diabetes Type 2 | Hepatitis B, Chronic | Bullous Pemphigoid | Anterior Segment Dysgenesis | Agnathia-Otocephaly Complex | Diabetes Insipidus | Antenatal Bartter Syndrome Type 1 | Adenomyosis | Osteogenesis Imperfecta Type V | Sporadic Hemiplegic Migraine | Behcet's Disease | Eczema | Preaxial Polydactyly | Antley-Bixler Syndrome | Milk Allergy | Vitamin B12 Deficiency | Thyroid Dysgenesis | Hypersomnia | Fontaine Progeroid Syndrome | Parapsoriasis | Mastitis | Steel Syndrome | Bietti Crystalline Dystrophy | Liver Failure | Renal Failure | Charcot-Marie-Tooth Disease Type 4B1 | Arthritis | Thyroid Dyshormonogenesis | Hypotonia-cystinuria Syndrome | Progressive Myoclonic Epilepsy | Galactosialidosis | Joubert Syndrome | Joubert Syndrome 2 | Neurotoxicity | Hypertrophic Osteoarthropathy, Primary, Autosomal Recessive 2 | Spondyloarthritis | Rothmund-Thomson Syndrome | Skin Carcinoma | Osteoporosis-pseudoglioma Syndrome | Riboflavin Transporter Deficiency Neuronopathy | Pneumonia, Mycoplasma | Olmsted Syndrome | Optic Nerve Hypoplasia, Bilateral | Hypercholesterolemia | Myocardial Infarction | Hyperinsulinemia | Arteriosclerosis | Charcot-Marie-Tooth Disease, Type 1A | Hemangioma | Trachoma | Wolman Disease | Congenital Disorders Of Glycosylation Type II | Hypercholesterolemia, Familial | Dysferlinopathy | Brachial Plexus Neuropathy | Early Infantile Epileptic Encephalopathy 28 | Focal Segmental Glomerulosclerosis | Pierpont Syndrome | Hypertrophy | Syndactyly | Pyruvate Dehydrogenase Deficiency | Spondylo-megaepiphyseal-metaphyseal Dysplasia | CREST Syndrome | B-cell Prolymphocytic Leukemia | Palsy, Cerebral | Antiphospholipid Syndrome | Schizoaffective Disorder | Multifocal Motor Neuropathy | Frontotemporal Dementia With Amyotrophic Lateral Sclerosis | Progressive Osseous Heteroplasia | Encephalopathy, Ethylmalonic | Spondylolisthesis | Hemoglobinopathies | Globozoospermia | Galloway-Mowat Syndrome | Absence Epilepsy | Phenylketonuria | Myoclonus-dystonia Syndrome | Dental Caries | Polycystic Kidney, Autosomal Dominant | Uremia | Pierre Robin Syndrome | Coffin-Siris Syndrome | Loeys-Dietz Syndrome Type 4 | Pneumothorax | Proteasome-associated Autoinflammatory Syndrome 2 | Hypertensive Nephropathy | Mitochondrial DNA Depletion Syndrome, Myopathic Form | Cone Dystrophy | Loeys-Dietz Syndrome | Neurodegeneration With Brain Iron Accumulation | Juvenile Xanthogranuloma | Cancer, Skin | Eiken Syndrome | Hyperhomocysteinemia | Cheilitis | Renal-hepatic-pancreatic Dysplasia | Kawasaki Disease | Aldosteronism | Chylomicron Retention Disease | Tricho-hepato-enteric Syndrome | Methylmalonic Aciduria And Homocystinuria, CblC Type | Nicotine Addiction | Acromegaly | Hyperphenylalaninemia | Anorectal Malformations | Opisthorchiasis | Dementia | Gerstmann-Straussler-Scheinker Syndrome | Seizures | Hepatic Veno-occlusive Disease | Corneal Edema | Waardenburg Syndrome Type 1 | Ovarian Sex Cord-stromal Tumor | Hyperammonemia | Erythema Multiforme | Hypertrophic Osteoarthropathy, Primary, Autosomal Recessive 1 | Primary Carnitine Deficiency | Werner's Syndrome | Connective Tissue Disorders | Endometriosis | Congenital Heart Block | Wiskott-Aldrich Syndrome | Menetrier Disease | Heterotaxy | Blomstrand Osteochondrodysplasia | Ligneous Conjunctivitis | Pemphigus Vulgaris | Oculocutaneous Albinism Type 2 | Neurofibromatosis Type 2 | Jacobsen Syndrome | Bipolar Disorder | Medium-chain Acyl-CoA Dehydrogenase Deficiency | Arts Syndrome | Keratitis-ichthyosis-deafness Syndrome | Rift Valley Fever | Meningococcal Meningitis | Osteogenesis Imperfecta Type III | Lipoma | Spinocerebellar Ataxia Type 14