Cardiac Arrest

About the Disease
Cardiac Arrest, also known as cardiopulmonary arrest, is related to post-cardiac arrest syndrome and ventricular fibrillation, paroxysmal familial, 1, and has symptoms including angina pectoris, chest pain and edema. An important gene associated with Cardiac Arrest is CASQ2 (Calsequestrin 2), and among its related pathways/superpathways are Transport of inorganic cations/anions and amino acids/oligopeptides and Beta-2 adrenergic-dependent CFTR expression. The drugs Clonazepam and Propofol have been mentioned in the context of this disorder. Affiliated tissues include heart, brain and skeletal muscle, and related phenotypes are muscle and cardiovascular system

Common Targets
G9429 | AVPR1B | Voltage-Gated Sodium Channel Complex | Sodium channel (nonspecified subtype) | CALM1 | Neurotrophic Factor (nonspecified subtype) | AVPR2 | OXT | CIRBP | POU3F3 | Potassium Channels (nonspecified subtype) | Adrenoceptor (nonspecified subtype) | OXTR | SEMA3A | SCN5A | G5728 | CYP4A11 | NGF | AVPR1A | ADAR | SCN10A | Calcium channel (nonspecified subtype) | CALM2

Note: If you'd like to get a target analysis report for Cardiac Arrest, 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 Cardiac Arrest at a cost 90% lower than traditional approaches, please feel free to contact us at BD@silexon.ai.

Other Diseases

Juvenile Hyaline Fibromatosis | Wolfram Syndrome | Congenital Absence Of Vas Deferens | Glomerulonephritis | Lattice Corneal Dystrophy Type 1 | Tendinitis | Asthma, Exercise-induced | Hyperthermia, Malignant | Inflammatory Bowel Disease | Oligoastrocytoma | Varices | Oral Lichen Planus | Ehlers-Danlos Syndrome With Progressive Kyphoscoliosis, Myopathy, And Hearing Loss | Parapsoriasis | Sponastrime Dysplasia | Kashin-Beck Disease | Gerodermia Osteodysplastica | Sickle Cell Disease | Basal Ganglia Cerebrovascular Disease | Isovaleric Acidemia | Metabolic Syndrome | Early Infantile Epileptic Encephalopathy 4 | Mucolipidosis Type IV | Familial Retinal Arterial Macroaneurysm | HANAC Syndrome | Autism | Keratosis, Seborrheic | Periventricular Leukomalacia | Acromicric Dysplasia | Sleep Apnea | Pierson Syndrome | Autosomal Recessive Bestrophinopathy | Diabetic Neuropathy | Epidermolytic Palmoplantar Keratoderma | Syncope | Peutz-Jeghers Syndrome | Limb Girdle Muscular Dystrophy | Nephronophthisis | Dysmorphophobia | Toxoplasmosis | Ophthalmoplegia | Pneumoconiosis | Intermittent Claudication | Hereditary Mixed Polyposis Syndrome | Asperger Syndrome | Bernard-Soulier Syndrome | Subacute Sclerosing Panencephalitis | Schizoaffective Disorder | Ectodermal Dysplasia | Ureteropelvic Junction Obstruction | Double Outlet Right Ventricle | Rubinstein-Taybi Syndrome | Mevalonate Kinase Deficiency | Hyperparathyroidism | Diabetes Type 1 | Epilepsy | Pyruvate Decarboxylase Deficiency | Intestinal Obstruction | Trichothiodystrophy | Cohen Syndrome | Chediak-Higashi Syndrome | Blastoma, Pleuropulmonary | Campomelic Dysplasia | Transthyretin-related Amyloidosis | Obesity, Morbid | Pseudohypoaldosteronism | Low Tension Glaucoma | Pemphigoid | Waldenstrom Macroglobulinemia | Trichotillomania | Inflammatory Myopathy | Cutaneous Mastocytosis | Aldosterone Synthase Deficiency | 17-beta-hydroxysteroid Dehydrogenase X Deficiency | Myasthenia Gravis | Schizophrenia, Paranoid | Carpenter Syndrome | Epidermolysis Bullosa Simplex, Generalized | Down Syndrome | Pontocerebellar Hypoplasia | Ovarian Sex Cord-stromal Tumor | Spondylocostal Dysostosis | Tuberculosis | Primary Carnitine Deficiency | Porphyria, Acute Intermittent | Atopy | Stroke | Cri-du-chat Syndrome | Genee-Wiedemann Syndrome | Glucagonoma | Sengers Syndrome | Stickler Syndrome | Stromal Corneal Dystrophy | Hypertension, Renal | Esophagitis, Eosinophilic | Poirier-Bienvenu Neurodevelopmental Syndrome | Congenital Poikiloderma | Presbycusis | Kawasaki Disease | Diabetes Insipidus, Nephrogenic | Sarcomatoid Carcinoma Of The Lung | Papulopustular Rosacea | Hypersomnia | Larsen Syndrome | Ganglioneuroma | B-cell Chronic Lymphocytic Leukemia | Colitis, Microscopic | Adenosine Deaminase Deficiency | Measles | Xeroderma Pigmentosum Variant Type | Intestinal Hypomagnesemia 1 | Vitelliform Macular Dystrophy | Glycogen Storage Disease Type 1b | Hypertension, Renovascular | Arts Syndrome | Insulinoma | Lamellar Ichthyosis | Hypocalcemia | Lymphoproliferative Disease, X-linked | Primary Ovarian Insufficiency | Spinocerebellar Ataxia Type 1 | Familial Advanced Sleep Phase Syndrome | Pityriasis Rubra Pilaris | Hypertension, Pulmonary | Acne Vulgaris | Pelizaeus-Merzbacher Disease | Lesch-Nyhan Syndrome | Synpolydactyly | Achromatopsia | Dentinogenesis Imperfecta | Gastroenteritis, Eosinophilic | Cornelia De Lange Syndrome | Androgenic Alopecia | Osteitis | Osteogenesis Imperfecta Type II | Generalized Epilepsy And Paroxysmal Dyskinesia | Glycogen Storage Disease Type 0 | Glutaric Aciduria Type 1 | Neuropathy | Localized Scleroderma | Congenital Lipoid Adrenal Hyperplasia | Leukemia | Trigonocephaly | Glaucomatocyclitic Crisis | Infertility, Male | Myelodysplasia | Stuve-Wiedemann Syndrome | Nijmegen Breakage Syndrome | Diffuse Intrinsic Pontine Glioma | CEDNIK Syndrome | Dengue Hemorrhagic Fever | Hyperostosis | Neurofibromatosis-Noonan Syndrome | Liddle Syndrome | Keratocystic Odontogenic Tumor | Carpal Tunnel Syndrome | Osteoporosis-pseudoglioma Syndrome | Facioscapulohumeral Muscular Dystrophy | Rash | Periodontitis | Osteogenesis Imperfecta Type I | Vitamin D Deficiency | Meningeal Melanocytoma | Joubert Syndrome 2 | Language Disorders | Congenital Hypofibrinogenemia | Cerebral Amyloid Angiopathy | Bronchiectasis | Menkes Disease | Hydrocephalus, Normal Pressure | Prolidase Deficiency | Lafora Disease | Walker-Warburg Syndrome | Colitis | Central Core Disease | Knobloch Syndrome | Diabetes Insipidus | Thymoma, Malignant | Liver Failure, Acute Infantile | Myoclonus | Rolandic Epilepsy | Dysfibrinogenemia | Meconium Ileus | Dysferlinopathy | Agammaglobulinemia | Atopic Dermatitis | Hyperphosphatasia With Intellectual Disability Syndrome 4 | Progressive Myoclonic Epilepsy | Granular Corneal Dystrophy Type 1 | Nestor-Guillermo Progeria Syndrome | Heart Block | GAPO Syndrome | Brooke-Spiegler Syndrome | Craniopharyngioma | Creatine Deficiency Syndrome | Necrotizing Autoimmune Myopathy | Pleural Tuberculosis | Carbohydrate Metabolism Disorders | Choreoathetosis, Hypothyroidism, And Neonatal Respiratory Distress | Genitopatellar Syndrome | Panniculitis | Thrombotic Microangiopathy | Coronary Artery Disease | Situs Inversus | Alcoholism | Osteosarcoma | Dyskeratosis Congenita | Temporal Lobe Epilepsy | Camurati-Engelmann Disease | Mucolipidosis Type II | Chylomicron Retention Disease | Plasmacytoma | X-linked Creatine Transporter Deficiency | Charcot-Marie-Tooth Disease, Type 2A | Speech Disorders | Eiken Syndrome | Molybdenum Cofactor Deficiency | Niemann-Pick Disease | Pheochromocytoma | Trismus-pseudocamptodactyly Syndrome | Peripheral Neuropathy | Jawad Syndrome | Micro Syndrome | Holoprosencephaly | Infantile Spasm | Hypogammaglobulinemia | Cancer, Kidney | Sarcoma, Alveolar Soft Part | Nevus | Scleroderma | Angioimmunoblastic T-cell Lymphoma | Hypogonadism | Angiosarcoma Of The Breast | Poikiloderma With Neutropenia | Cerebellar Ataxia, Cayman Type | Eclampsia | NGLY1 Deficiency | Vitamin K Deficiency | Congenital Disorders Of Glycosylation Type II | Tracheal Disorders | Hereditary Coproporphyria | Liver Diseases | Tyrosine Hydroxylase Deficiency | Neuroma | Retinal Degeneration | Pneumonia, Mycoplasma | Cholecystitis | Antiphospholipid Syndrome | Corneal Dystrophy | Spinocerebellar Ataxia Type 7 | Ectrodactyly | Congenital Nephrotic Syndrome | Familial Digital Arthropathy-brachydactyly | Sotos Syndrome | Oculopharyngeal Muscular Dystrophy | Mountain Sickness | Prader-Willi Syndrome | Neutropenia | Turner's Syndrome | Smith-Lemli-Opitz Syndrome | Diabetes Insipidus, Neurogenic | Peeling Skin Syndrome Type B | Blepharitis | Hypertension, Portal | Primary Torsion Dystonia | IgA Deficiency | Argininosuccinic Aciduria | Goldenhar Syndrome | Avellino Corneal Dystrophy | Brugada Syndrome 1 | Macular Degeneration | Beta-Propeller Protein-associated Neurodegeneration | Meckel-Gruber Syndrome | Van Der Knaap Disease | Galactosialidosis | Joubert Syndrome | Renal Dysplasia | Aromatic L-amino Acid Decarboxylase Deficiency | Alzheimer Disease, Late Onset | Hypothyroidism | Heterotaxy | Hypertelorism | Erdheim-Chester Disease | Polycystic Ovary Syndrome | Urofacial Syndrome | Gestational Trophoblastic Disease | Hypospadias | Miyoshi Myopathy | Immunoproliferative Disorders | Non-Langerhans Cell Histiocytosis | Holt-Oram Syndrome | Apraxia | Guanidinoacetate Methyltransferase Deficiency | Arteriosclerosis | Multiple Epiphyseal Dysplasia | DEND Syndrome | Blomstrand Osteochondrodysplasia | Chondroma | Myoclonus-dystonia Syndrome | Glycogen Storage Disease Type 0, Muscle | Hyperkeratosis | Hyperekplexia | Emery-Dreifuss Muscular Dystrophy | Osteoporosis | Diastrophic Dysplasia | Sandhoff Disease | MIRAGE Syndrome | Craniometaphyseal Dysplasia | Sclerosing Cholangitis | Chromosome 16p11.2 Deletion Syndrome | Acanthosis Nigricans | Trachoma | Rotor Syndrome | 3-M Syndrome | Nicotine Addiction | Hereditary Pyropoikilocytosis | Hepatic Veno-occlusive Disease | Erythropoietic Protoporphyria | Glycogen Storage Disease Type 6 | Babesiosis | Spinocerebellar Ataxia Type 40 | Autosomal Recessive Spastic Paraplegia Type 75 | Renal Hypomagnesemia 3 | Scabies | Systemic Mastocytosis | Arthritis, Gouty | Ichthyosis Bullosa Of Siemens | Myositis | ADNP Syndrome | Panuveitis | Intracranial Hypertension | Veno-occlusive Disease | Blau Syndrome | Hepatitis B, Chronic | Smoldering Myeloma | Spasticity | Polycystic Liver | Hypokalemia | Fanconi Syndrome | H Syndrome | CHARGE Syndrome | Early Infantile Epileptic Encephalopathy | Atelosteogenesis Type 2 | Optic Neuritis | Multiple Sclerosis | Disseminated Intravascular Coagulation | Congenital Stromal Corneal Dystrophy | Chorea-acanthocytosis | Abetalipoproteinemia | Juvenile Myelomonocytic Leukemia | Biotinidase Deficiency | Azoospermia | Hyperinsulinism-hyperammonemia Syndrome | Norrie Disease | Vaginitis | Familial Glucocorticoid Deficiency | Compartment Syndrome | Acute Tubular Necrosis | Hypodontia | Cholangiocarcinoma | Meningococcal Infections | Combined Pituitary Hormone Deficiency | TARP Syndrome | Trichomegaly | Ulcerative Colitis | Mitochondrial DNA Depletion Syndrome, Myopathic Form | Hypercholesterolemia | 3C Syndrome | Sezary Syndrome | Hypertrophic Osteoarthropathy, Primary, Autosomal Recessive 1 | Prostatitis | Schnyder Crystalline Corneal Dystrophy | Fahr Disease | Demyelinating Diseases | Sarcoma, Ewing | Megaloblastic Anemia | Congenital Dyserythropoietic Anemia Type 4 | Gaucher Disease | Hyperbilirubinemia | Congenital Torticollis | Kindler Syndrome | Hydrocephalus | Dowling-Degos Disease | Influenza | Adrenoleukodystrophy, X-linked | GM2-gangliosidosis AB Variant | Vestibular Disease | Common Cold | Macrodactyly | Pyelonephritis | Retinoschisis | Intestinal Pseudo-obstruction | Thyroiditis | Epidermolytic Ichthyosis, Annular | Dystonia Musculorum Deformans | Strabismus | Cantu Syndrome | Mycosis Fungoides | Polymicrogyria | Roberts Syndrome