Coronary Restenosis

About the Disease
Coronary Restenosis is related to coronary stenosis and atherosclerosis susceptibility. An important gene associated with Coronary Restenosis is ACE (Angiotensin I Converting Enzyme), and among its related pathways/superpathways are Malignant pleural mesothelioma and PI3K-Akt signaling pathway. The drugs Celecoxib and Miconazole have been mentioned in the context of this disorder. Affiliated tissues include endothelial, smooth muscle and liver, and related phenotypes are homeostasis/metabolism and cellular

Common Targets
ADAMTS7 | FLAD1 | NR4A1 | TBL1XR1 | MASP2 | GUSB | AGPAT3 | P2RY12 | HDAC4 | MIR146A | G7422 | MIR196A2 | CRP

Note: If you'd like to get a target analysis report for Coronary Restenosis, or if you are interested to learn how our AI-powered BDE-Chem can design therapeutic molecules to interact with the target(s) above against the disease of Coronary Restenosis at a cost 90% lower than traditional approaches, please feel free to contact us at BD@silexon.ai.

Other Diseases

Glycogen Storage Disease | Infantile Refsum Disease | Erythromelalgia | Spinocerebellar Ataxia Type 7 | Van Der Knaap Disease | Gynecomastia | Insulinoma | Charcot-Marie-Tooth Disease, Type 2 | Lymphoma, AIDS-related | Esophageal Motility Disorders | Splenomegaly | Lung Diseases | Isobutyryl-CoA Dehydrogenase Deficiency | Odonto-onycho-dermal Dysplasia | Purpura, Thrombotic Thrombocytopenic | Iron Overload | Familial Dysautonomia | Acute Chest Syndrome | Osteosarcoma | Epilepsy | Silicosis | Adenoma, Pleomorphic | Essential Fructosuria | Osteopetrosis | Mucolipidosis Type II | Schaaf-Yang Syndrome | Blau Syndrome | Pyruvate Decarboxylase Deficiency | Tyrosinemia Type 1 | Hypertension, Renovascular | Transcobalamin Deficiency | Leprosy | Carbamoyl Phosphate Synthetase I Deficiency | Vertebrobasilar Insufficiency | Proteus Syndrome | Hyperostosis | Sleep Apnea, Obstructive | Neurofibromatosis Type 1 | Addison Disease | Dementia, Vascular | Cholecystitis | Osteoglophonic Dysplasia | Mucolipidosis Type IV | Intermittent Claudication | Seizures | Renal Dysplasia | Cancer, Bladder | Tendinopathy | Hairy Cell Leukemia | Cannabis Abuse | Distal Myopathy | Leukocyte Adhesion Deficiency Type 1 | Hypertension | Prolidase Deficiency | Spitzoid Melanoma | Orotic Aciduria | Paternal Uniparental Disomy Of Chromosome 14 | Chanarin-Dorfman Syndrome | Juvenile Hyaline Fibromatosis | Biotinidase Deficiency | Olmsted Syndrome | Gestational Trophoblastic Disease | CREST Syndrome | Cartilage Disorders | Liver Diseases | Optic Nerve Hypoplasia, Bilateral | Scleroderma | Osteoporosis, Postmenopausal | Sengers Syndrome | Peripheral T-cell Lymphoma | Anuria | Epicondylitis | Asthma | Veno-occlusive Disease | Pseudohypoparathyroidism Type 2 | Renal Tubular Dysgenesis | 3-methylglutaconic Aciduria Type IV | Localized Scleroderma | Carney-Stratakis Syndrome | Epidermolysis Bullosa Simplex With Mottled Pigmentation | Coma | Dystonia Musculorum Deformans | Epidermolysis Bullosa Simplex, Localized | Familial Isolated Hyperparathyroidism | Eiken Syndrome | Situs Inversus | Congenital Sodium Diarrhea | Neurotoxicity | Sjogren Syndrome | Saethre-Chotzen Syndrome | Achromatopsia | Hepatitis B, Chronic | Sensorineural Hearing Loss | Crouzon Syndrome With Acanthosis Nigricans | Hemophilia | Neurofibromatosis | Hereditary Sensory And Autonomic Neuropathy | Milk Allergy | Urethritis | Glutaric Aciduria Type 3 | Arts Syndrome | Benign Hereditary Chorea | Epilepsy, Generalized | Pseudohermaphroditism | Leiomyosarcoma | Gyrate Atrophy Of The Choroid And Retina | Charcot-Marie-Tooth Disease, Type 6 | Nestor-Guillermo Progeria Syndrome | Hypertension, Essential | Juvenile Polyposis | Autoimmune Autonomic Ganglionopathy | Kabuki Syndrome 2 | Richter's Syndrome | Bardet-Biedl Syndrome | Connective Tissue Disorders | Constipation | Hyperhomocysteinemia | Priapism | Agranulocytosis | Long QT Syndrome Type 2 | Macular Degeneration | Hepatoblastoma | Antisocial Personality Disorder | Canavan Disease | Botulism | Aicardi-Goutieres Syndrome | Erythrokeratodermia Variabilis | Microcephaly, Seizures, And Developmental Delay | Multicentric Carpotarsal Osteolysis Syndrome | Cone Dystrophy | Lactose Intolerance | Osteoporosis-pseudoglioma Syndrome | Phosphoglycerate Dehydrogenase Deficiency | Ocular Albinism Type 1 | Eosinophilia | Retinopathy, Diabetic | Pierson Syndrome | Acanthosis Nigricans | Schnitzler Syndrome | Hypercalciuria | Familial Episodic Pain Syndrome | Benign Familial Neonatal Convulsions | Endometriosis | Allergic Contact Dermatitis | Congenital Dyserythropoietic Anemia Type 1 | Carcinoma In Situ | Schwannomatosis | PASLI Disease | Corneal Edema | Astigmatism | Sarcoma, Alveolar Soft Part | Dyggve-Melchior-Clausen Disease | Diabetic Encephalopathy | Neural Tube Defect | Esophagitis, Eosinophilic | Chondrodysplasia Punctata 1, X-linked Recessive | Thalassemia, Beta | Usher Syndrome Type I | Inflammatory Bowel Disease | Rickets | Geleophysic Dysplasia | Toxic Epidermal Necrolysis | Peripheral Neuropathy | Spondyloepiphyseal Dysplasia Tarda, X-linked | Cancer, Prostate | Hemochromatosis | Pulmonary Veno-occlusive Disease | Cancer, Brain | Seizures-scoliosis-macrocephaly Syndrome | Mesial Temporal Lobe Epilepsy With Hippocampal Sclerosis | Atopy | Antiphospholipid Syndrome | Pigment Dispersion Syndrome | Birk-Barel Syndrome | Pre-eclampsia | Hypothalamic Obesity | Split Hand-foot Malformation | McLeod Syndrome | Sarcoma, Endometrial Stromal | Crimean-Congo Hemorrhagic Fever | Distal Myopathy 2 | Gangliosidosis, GM1 | IgA Nephropathy | Agnathia-Otocephaly Complex | Hyperammonemia | Inborn Errors Of Metabolism | Cholangitis | NGLY1 Deficiency | Metanephric Adenoma | Warsaw Breakage Syndrome | Myofibrillar Myopathy | Primary Progressive Aphasia | Atopic Dermatitis | Esophageal Adenocarcinoma | Cancer, Lung | Congenital Diaphragmatic Hernia | Hypophosphatemic Rickets, Autosomal Recessive, 1 | Lathosterolosis | Pemphigoid | Autoimmune Disease | Benign Familial Infantile Seizures | Rheumatoid Arthritis | Oligoasthenoteratozoospermia | Encephalopathy, Hepatic | Thalassemia | Macrodactyly | Obesity | Transthyretin-related Amyloidosis | Exotropia | Clouston Hidrotic Ectodermal Dysplasia | Esophageal Carcinoma | Echinococcosis | Oculocutaneous Albinism | Tyrosinemia Type 2 | Dementia | Amelogenesis Imperfecta | Erectile Dysfunction | Cancer, Breast | Progressive Encephalopathy-optic Atrophy Syndrome | Osteomalacia | Acute Anterior Uveitis | Spondyloperipheral Dysplasia | Charcot-Marie-Tooth Disease Type 2T | Miyoshi Myopathy | Acromicric Dysplasia | Spinocerebellar Ataxia Type 27 | Hemolytic Anemia | Liver Failure, Acute Infantile | Uveitis | Meningioma | Osteoarthritis | Tularemia | Combined Malonic And Methylmalonic Acidemia | ADNP Syndrome | Hypertension, Pulmonary | Spinal Muscular Atrophy With Progressive Myoclonic Epilepsy | CEDNIK Syndrome | Mosaic Variegated Aneuploidy Syndrome 2 | Follicular Dendritic Cell Sarcoma | CDKL5 Deficiency Disorder | Hypertrophic Osteoarthropathy, Primary, Autosomal Recessive 1 | Subacute Sclerosing Panencephalitis | Glycogen Storage Disease Type 0, Muscle | Retinitis Pigmentosa | Pituitary Stalk Interruption Syndrome | Familial Pheochromocytoma-paraganglioma | Epidermolytic Hyperkeratosis | 3-M Syndrome | Uterine Leiomyoma | Hyperphosphatasia With Intellectual Disability Syndrome 4 | Schizoaffective Disorder | CHARGE Syndrome | Congenital Aniridia | Wiskott-Aldrich Syndrome | Proximal Symphalangism | T-cell Lymphoma, Subcutaneous Panniculitis-like | Pseudoexfoliation Syndrome | Spinocerebellar Ataxia Type 20 | Hepatorenal Syndrome | Familial Glucocorticoid Deficiency | Esthesioneuroblastoma | Melanoma, Malignant | Adenosine Deaminase Deficiency | Congenital Nephrotic Syndrome | Glioblastoma Multiforme | Skin Carcinoma | Eccrine Porocarcinoma | Infantile Nephropathic Cystinosis | Huntington's Disease | Hypertelorism | Pycnodysostosis | Chronic Periodontitis | Carcinoma, Merkel Cell | Acute Kidney Injury | Spondyloarthritis | Ligneous Conjunctivitis | Fibromyalgia | Encephalitis, Tick-borne | Spondylo-megaepiphyseal-metaphyseal Dysplasia | Glycogen Storage Disease Type 9 | Bernard-Soulier Syndrome | Hyperbilirubinemia | Central Pain Syndrome | Loeys-Dietz Syndrome Type 4 | Aromatic L-amino Acid Decarboxylase Deficiency | Hemoglobinopathies | Encephalocele | Succinic Semialdehyde Dehydrogenase Deficiency | Pyelonephritis | Keratosis | Pearson Syndrome | Chordoid Glioma | Bacterial Meningitis | Interstitial Lung Diseases | HUPRA Syndrome | Retinal Vasculitis | Multiple Sulfatase Deficiency | Relapsing Polychondritis | Vitreoretinal Degeneration, Snowflake Type | Carcinoma, Transitional Cell | Infectious Diarrhea | Pleural Tuberculosis | Overactive Bladder | Prostatitis | Mitochondrial Cytopathy | Antisynthetase Syndrome | Keratosis, Actinic | Basal Cell Nevus Syndrome | Camptocormia | Pancreatitis, Chronic | Angioedema, Hereditary | Aldosterone Deficiency | Optic Atrophy 2 | Acute Lymphocytic Leukemia | Ollier Disease | Cyst | HIBCH Deficiency | Gastroenteritis, Eosinophilic | Xeroderma Pigmentosum | Cleidocranial Dysplasia | Mitochondrial Myopathy | Parkinson Disease 6, Autosomal Recessive Early-onset | Carcinoid Syndrome | Hypercholesterolemia, Familial | Li-Fraumeni Syndrome | Fundus Albipunctatus | Coronary Restenosis | Lamellar Ichthyosis | Seborrheic Dermatitis | Cluster Headache | Meconium Ileus | Nicolaides-Baraitser Syndrome | Erythema Multiforme | Glycogen Storage Disease Type 1a | Cancer, Skin | Liver Failure | Platyspondylic Lethal Skeletal Dysplasia, Torrance Type | Chondrodysplasia Punctata 2, X-linked Dominant | Spinocerebellar Ataxia Type 42 | Kidney Stones | Alkaptonuria | Mannosidase Deficiency Diseases | Ehlers-Danlos Syndrome | Schistosomiasis | Takayasu's Arteritis | Optic Neuropathy | McCune-Albright Syndrome | Leukemia | Retinal Detachment | Fibronectin Glomerulopathy | Waardenburg Syndrome Type 1 | Alcoholism | Muscle Wasting | Dysthymia | Schizotypal Personality Disorder | Histiocytosis | Xeroderma Pigmentosum Variant Type | Basal Ganglia Disease, Biotin-responsive | Arteriosclerosis | Nicotine Dependence | Pfeiffer Syndrome | Tardive Dyskinesia | Pulmonary Stenosis | Leukoencephalopathy, Progressive Multifocal | Christianson Syndrome | Crohn's Disease | Familial Digital Arthropathy-brachydactyly | Robinow Syndrome | Hyperparathyroidism, Secondary | Early Infantile Epileptic Encephalopathy 28 | Polycystic Kidney, Autosomal Dominant | Spinocerebellar Ataxia Type 40 | Arthropathy | Retinal Telangiectasia | Seasonal Mood Disorder | Stroke, Hemorrhagic | Costello Syndrome | Bietti Crystalline Dystrophy | Diabetic Nephropathy | Hidradenitis | Malignant Fibrous Histiocytoma | Pierre Robin Syndrome | Hidradenitis Suppurativa | Optic Nerve Diseases | Charcot-Marie-Tooth Disease, Type 2A | Bloom Syndrome | Multiple Mitochondrial Dysfunctions Syndrome Type 1 | Heterotaxy | Prediabetes | Niemann-Pick Disease | Apert Syndrome | Polyarteritis Nodosa | Nephritis, Interstitial | Holoprosencephaly | Pleurisy | Proctitis | Ameloblastoma | Nemaline Myopathy | Pseudoachondroplasia | Waldenstrom Macroglobulinemia