Cardiac Sarcoidosis

About the Disease
Cardiac Sarcoidosis is related to sarcoidosis 1 and skin sarcoidosis. An important gene associated with Cardiac Sarcoidosis is TNF (Tumor Necrosis Factor), and among its related pathways/superpathways are Keratinization and DREAM Repression and Dynorphin Expression. The drugs Prednisolone phosphate and Prednisolone acetate have been mentioned in the context of this disorder. Affiliated tissues include heart, lymph node and lung, and related phenotypes are muscle and cardiovascular system

Common Targets
TSPO

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

Other Diseases

Peeling Skin Syndrome Type B | Pathological Gambling | Acral Lentiginous Melanoma | Beta-Propeller Protein-associated Neurodegeneration | Menetrier Disease | Desmosterolosis | Duodenal Atresia | Acne | Treacher Collins Syndrome | Nephropathy | Pityriasis Rubra Pilaris | Hepatitis, Chronic | Rheumatoid Arthritis | Dyslexia | Hepatoblastoma | Gynecomastia | Histoplasmosis | Plasma Cell Dyscrasia | Urea Cycle Disorder | Liddle Syndrome | Eating Disorder | Alopecia Areata | Chronic Myeloid Leukemia | Cholecystitis | Epilepsy Of Infancy With Migrating Focal Seizures | Lactose Intolerance | Autoimmune Hemolytic Anemia | Behavioral Variant Of Frontotemporal Dementia | Osteogenesis Imperfecta Type V | Pearson Syndrome | Cutaneous Lupus Erythematosus | Gray Platelet Syndrome | Paternal Uniparental Disomy Of Chromosome 14 | Pancreatitis, Chronic | Cervicitis | Basan Syndrome | Gingivitis | Niemann-Pick Disease | Progressive Familial Intrahepatic Cholestasis | Cardiomyopathy, Dilated, 1L | Arts Syndrome | Limb Girdle Muscular Dystrophy | Persistent Mullerian Duct Syndrome | Tyrosinemia | Asthma, Exercise-induced | Malaria, Cerebral | Macrodactyly | Dystonia Musculorum Deformans | Synpolydactyly | Hypertensive Retinopathy | Hepatitis D | Retinopathy, Diabetic | Blepharitis | Overactive Bladder | Methylmalonic Acidemia | Schizophrenia | Myositis | COACH Syndrome | Myelodysplasia | Transthyretin-related Amyloidosis | Fibrosis | Phenylketonuria II | Graves Disease | Familial Mediterranean Fever | Burn-McKeown Syndrome | Werner's Syndrome | Trichorhinophalangeal Syndrome | Pyruvate Dehydrogenase Deficiency | Carcinoma, Signet Ring Cell | Kleine-Levin Syndrome | Panniculitis | Chronic Lymphocytic Leukemia | Antenatal Bartter Syndrome Type 1 | Carcinoma, Transitional Cell | Hemangioma | Varicocele | Gitelman Syndrome | Arthritis, Reactive | Syncope | Bloom Syndrome | Muckle-Wells Syndrome | Hyperphenylalaninemia | Arthritis | Oligodendroglioma | Usher Syndrome Type III | Corneal Edema | Liver Failure, Acute Infantile | Central Pain Syndrome | Fukuyama Congenital Muscular Dystrophy | Plasma Cell Leukemia | Neuroendocrine Cancer | Ocular Surface Squamous Neoplasia | Pneumothorax | Prostatitis | Chronic Inflammatory Demyelinating Polyneuropathy | Norrie Disease | Tremor | Venous Insufficiency | Early Infantile Epileptic Encephalopathy 1 | Pneumoconiosis | Allergic Contact Dermatitis | Gangliosidosis, GM1 | Dubin-Johnson Syndrome | Acute Coronary Syndrome | Sick Sinus Syndrome 1 | Wiskott-Aldrich Syndrome | Epidermolysis Bullosa Simplex With Mottled Pigmentation | Carcinoma, Squamous Cell | Benign Familial Neonatal Convulsions | Familial Glucocorticoid Deficiency | Lipid Storage Diseases | Acute Kidney Injury | Non-Langerhans Cell Histiocytosis | Lassa Fever | Aldosterone Synthase Deficiency | Hypokalemia | Carcinoid Tumor | Adenosine Deaminase Deficiency | Agnathia-Otocephaly Complex | Benign Hereditary Chorea | Muscular Dystrophy | Amyloidosis | Sickle Cell Anemia | Fetal Alcohol Syndrome | Cerebrovascular Disorders | Paraganglioma, Carotid Body | 3-hydroxy-3-methylglutaric Aciduria | Mabry Syndrome | Thyroiditis, Autoimmune | Multiple Sclerosis, Chronic Progressive | Growth Hormone Excess | Spinal Muscular Atrophy Type 2 | Hypogammaglobulinemia | Hyperlipidemia | Papulopustular Rosacea | Cryptococcal Meningitis | Androgenic Alopecia | Osteogenesis Imperfecta Type III | Primary Erythromelalgia | Neonatal Progeroid Syndrome | Familial Retinal Arterial Macroaneurysm | Autosomal Recessive Bestrophinopathy | Hypertrophic Osteoarthropathy, Primary, Autosomal Recessive 2 | Subcortical Band Heterotopia | Hypopituitarism | Osteochondroma | Atrioventricular Septal Defect | Glycogen Storage Disease Type 0 | Nanophthalmos | Hyperparathyroidism, Primary | Cancer, Breast | Hypotonia-cystinuria Syndrome | Choreoathetosis, Hypothyroidism, And Neonatal Respiratory Distress | Methylmalonic Aciduria And Homocystinuria, CblC Type | Seasonal Mood Disorder | Conjunctivitis, Allergic | Myocardial Infarction | Diamond-Blackfan Anemia | Birk-Barel Syndrome | Immunoproliferative Disorders | Hereditary Folate Malabsorption | VEXAS Syndrome | Diabetes Mellitus, Transient Neonatal | Lymphoma, Follicular | Vasculitis | Disseminated Superficial Actinic Porokeratosis | Waardenburg Syndrome Type 4 | Multicystic Renal Dysplasia | Cyclic Vomiting Syndrome | Lymphedema | Spinocerebellar Ataxia Type 1 | Enterocolitis, Necrotizing | Metaphyseal Chondrodysplasia, Schmid Type | Sandhoff Disease | Bleeding Disorder Due To CalDAG-GEFI Deficiency | Lymphomatoid Granulomatosis | Acne Vulgaris | Glutathione Synthetase Deficiency | Actinomycetoma | Varices | Cancer, Colon | Purpura, Thrombotic Thrombocytopenic | Congenital Aniridia | Giant Cell Glioblastoma | Renal Dysplasia | Congenital Myasthenic Syndrome | Low Tension Glaucoma | Vitamin K Deficiency | Hartnup Disease | Osteoarthritis | Uremic Pruritus | Nephroblastoma | Ischemia | L-2-Hydroxyglutaric Aciduria | Hemolytic Uremic Syndrome | Pyelonephritis | Rotor Syndrome | Ehlers-Danlos Syndrome With Progressive Kyphoscoliosis, Myopathy, And Hearing Loss | Long QT Syndrome Type 1 | Corticobasal Syndrome | Tangier Disease | Synovitis | Autonomic Neuropathy | Epidermolysis Bullosa | Smith-Magenis Syndrome | Mannosidase Deficiency Diseases | Autoimmune Disease | Waardenburg Syndrome Type 2E | Turner's Syndrome | Optic Neuropathy | Hypotrichosis Simplex | Mitochondrial DNA Depletion Syndrome | Endometrial Hyperplasia | Postpartum Depression | Acute Generalized Exanthematous Pustulosis | GAPO Syndrome | X-linked Acrogigantism | Takayasu's Arteritis | Prolidase Deficiency | Porphyria | Hypophosphatemic Rickets With Hypercalciuria, Hereditary | Multiple Sulfatase Deficiency | Saethre-Chotzen Syndrome | Triple A Syndrome | Platelet Disorders | Antiphospholipid Syndrome | Melanoma, Malignant | Silver-Russell Syndrome | Eosinophilic Asthma | Pseudohypoparathyroidism Type 1B | Acromesomelic Dysplasia | Chondrodysplasia Punctata 2, X-linked Dominant | Periventricular Nodular Heterotopia | Borjeson-Forssman-Lehmann Syndrome | Polycystic Liver | Split Hand-foot Malformation | Pompe Disease | Renal Hypomagnesemia 3 | Sarcoidosis, Pulmonary | Antisynthetase Syndrome | LMNA-related Congenital Muscular Dystrophy | Brachial Plexus Neuropathy | Wiedemann-Steiner Syndrome | Joubert Syndrome 2 | Reye Syndrome | Chronic Leukemia | Dementia | Chronic Periodontitis | Epithelioid Hemangioma | Agammaglobulinemia | Histiocytic Sarcoma | Angioedema | Obsessive-compulsive Disorder | Pemphigoid | Vici Syndrome | Intermittent Claudication | Snyder-Robinson Syndrome | Sengers Syndrome | Onchocerciasis | Chronic Mucocutaneous Candidiasis | Hemangioblastoma | Analgesia | Endometriosis | Borderline Personality Disorder | Gastric Atrophy | Atrial Septal Defect | Nasodigitoacoustic Syndrome | Achromatopsia | Tetanus | Hyperlipidemia Type V | Familial Dysautonomia | Bicuspid Aortic Valve | Hermansky-Pudlak Syndrome | Poretti-Boltshauser Syndrome | Hypocalcemia | Spondylocarpotarsal Synostosis Syndrome | Craniosynostosis | Pemphigus Foliaceus | Intestinal Pseudo-obstruction | Sertoli Cell-only Syndrome | McCune-Albright Syndrome | Phenylketonuria | Cancer, Brain | Autonomic Nervous System Disorders | Heart Block | Left Ventricular Noncompaction | Oligoasthenoteratozoospermia | Hypercholesterolemia | Distal Spinal Muscular Atrophy | Polymyositis | Bronchitis | Congenital Disorders Of Glycosylation | Basal Ganglia Disease, Biotin-responsive | Spondylo-ocular Syndrome | Hypothyroidism | Mitochondrial Cytopathy | Wolfram Syndrome | Incontinentia Pigmenti | Learning Disability | Intracerebral Hemorrhage | Neurofibromatosis Type 1 | Atopic Dermatitis | Adenoid Cystic Carcinoma | Pontocerebellar Hypoplasia | Hashimoto Thyroiditis | Jaundice, Obstructive | Amelogenesis Imperfecta | Nemaline Myopathy | Pendred Syndrome | Spinocerebellar Ataxia Type 2 | Micropenis | Progressive Myoclonic Epilepsy | Acute Lung Injury | Otopalatodigital Syndrome Type 2 | Anuria | Familial Hypobetalipoproteinemia | Microphthalmia | Cluster Headache | Sarcoma, Alveolar Soft Part | Lissencephaly 2 | Hemochromatosis Type 1 | Optic Atrophy 2 | Acute Chest Syndrome | Arthritis, Gouty | Gangliosidosis | Abetalipoproteinemia | Dermatofibrosarcoma | Congenital Hereditary Endothelial Dystrophy Type II | Meningitis | Myotonia | Chordoma | Nance-Horan Syndrome | Eosinophilia | Cryptorchidism | Waardenburg Syndrome Type 1 | Gardner Syndrome | Hypermethioninemia | Kashin-Beck Disease | Lattice Corneal Dystrophy | Rett Syndrome | Inflammatory Myopathy | Hyperkeratosis | Corneal Neovascularization | Antithrombin III Deficiency | Peritonitis | Von Willebrand Disease | Iron Deficiency Anemia | Shprintzen-Goldberg Syndrome | Macular Degeneration | Fabry's Disease | Craniofacial Dysostosis | Postaxial Polydactyly | Glutaric Aciduria Type 2 | Keratopathy | Charcot-Marie-Tooth Disease Type 2D | Colitis, Microscopic | Mitochondrial DNA Depletion Syndrome, Myopathic Form | Autoimmune Interstitial Lung, Joint, And Kidney Disease | Cantu Syndrome | Charcot-Marie-Tooth Disease, Type 2C | Membranous Nephropathy | Episodic Ataxia | Takenouchi-Kosaki Syndrome | Pancytopenia | Osteoglophonic Dysplasia | Arrhythmogenic Right Ventricular Cardiomyopathy | Leishmaniasis, Visceral | Malaria | Diabetic Neuropathy | Ependymoma | Transcobalamin Deficiency | Spinocerebellar Ataxia | Craniolenticulosutural Dysplasia | Hydrops Fetalis | Kabuki Syndrome 2 | Ataxia-ocular Apraxia 2 | Megalencephaly | Thanatophoric Dysplasia Type 1 | Dyslipidemia | Vitelliform Macular Dystrophy | GM2-gangliosidosis AB Variant | Osteogenesis Imperfecta | Pilomatrix Carcinoma | Hypoalbuminemia | Smith-Kingsmore Syndrome | VACTERL Association | Torticollis | Cholelithiasis | Depression | Paroxysmal Nocturnal Hemoglobinuria | Tetraplegia | Schnyder Crystalline Corneal Dystrophy | Kernicterus | Encephalopathy | Hairy Cell Leukemia | Fraser Syndrome | Barrett Esophagus | Blepharoconjunctivitis | Spondyloepiphyseal Dysplasia Tarda, X-linked | Spondyloperipheral Dysplasia