Endocarditis
Endocarditis
About the Disease
Endocarditis is related to infective endocarditis and libman-sacks endocarditis, and has symptoms including angina pectoris, chest pain and edema. An important gene associated with Endocarditis is CRP (C-Reactive Protein), and among its related pathways/superpathways are Complement cascade and Overview of interferons-mediated signaling pathway. The drugs Imipenem and Ceftriaxone have been mentioned in the context of this disorder. Affiliated tissues include heart, spleen and skin, and related phenotypes are no effect and no effect
Common Targets
SELE | IL10 | G7124 | IL1B | G3569 | ICAM1 | G7099 | EPX
![疾病靶点研报](../img/disease-target-analysis-report.jpg)
Note: If you'd like to get a target analysis report for Endocarditis, 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 Endocarditis at a cost 90% lower than traditional approaches, please feel free to contact us at BD@silexon.ai.
Other Diseases
Pituitary Stalk Interruption Syndrome | Paraganglioma, Carotid Body | Renal-hepatic-pancreatic Dysplasia | Ganglioneuroma | Cherubism | Prolidase Deficiency | Blastomycosis | Autism | Malonyl-CoA Decarboxylase Deficiency | Asperger Syndrome | Atopy | Cat Eye Syndrome | Adenoma, Villous | Ichthyosis Bullosa Of Siemens | Scleroderma | Retinopathy, Diabetic | Renal Tubular Dysgenesis | Cold Agglutinin Disease | Epidermolysis Bullosa Simplex With Mottled Pigmentation | Progressive External Ophthalmoplegia | Chronic Granulomatous Disease | Cervical Dystonia | Stargardt Disease | Osteogenesis Imperfecta Type IV | Cramp Fasciculation Syndrome | Hypogonadism | Gigantism | Encephalopathy, Glycine | Retinal Diseases | Ataxia-hypogonadism-choroidal Dystrophy Syndrome | Autoimmune Interstitial Lung, Joint, And Kidney Disease | Mitochondrial DNA Depletion Syndrome, Myopathic Form | Turner's Syndrome | Dementia, Vascular | Mitochondrial DNA Depletion Syndrome 13 | Epilepsy | Mixed Connective Tissue Disease | Retinitis | Hypoalbuminemia | Paroxysmal Nocturnal Hemoglobinuria | Non-Langerhans Cell Histiocytosis | Twin-to-twin Transfusion Syndrome | Erdheim-Chester Disease | Nemaline Myopathy 8 | Protein S Deficiency | Cryptosporidiosis | Encephalitis, Tick-borne | L-2-Hydroxyglutaric Aciduria | Granular Corneal Dystrophy | Waardenburg Syndrome | Succinic Semialdehyde Dehydrogenase Deficiency | Myosin Storage Myopathy | Glomerulonephritis | Mitochondrial DNA Depletion Syndrome, Hepatocerebral Form | IgA Nephropathy | Congenital Sodium Diarrhea | Plasma Cell Leukemia | Vertigo | GATA2 Deficiency | Multiple Sulfatase Deficiency | Persistent Hyperplastic Primary Vitreous | Thalassemia, Beta | Syncope | Loeys-Dietz Syndrome Type 4 | Adenosine Deaminase Deficiency | Cutis Laxa | Nemaline Myopathy 10 | Panniculitis | Ulcerative Colitis | Immunoproliferative Disorders | Acute Coronary Syndrome | Antisynthetase Syndrome | Diabetic Neuropathy | Early Infantile Epileptic Encephalopathy 1 | Congenital Dysfibrinogenemia | Moyamoya Disease | Hereditary Neuropathy With Liability To Pressure Palsies | Nephritis, Interstitial | Chronic Granulomatous Disease, X-linked | Cardiofaciocutaneous Syndrome | Choriocarcinoma | Obesity | Osteopathia Striata With Cranial Sclerosis | Papulopustular Rosacea | Triphalangeal Thumb-polysyndactyly Syndrome | Primary Carnitine Deficiency | Vascular Cognitive Impairment | Pityriasis Rubra Pilaris | Keratitis-ichthyosis-deafness Syndrome | Axenfeld-Rieger Syndrome | Sleep Apnea, Central | SAPHO Syndrome | Schnitzler Syndrome | Macular Corneal Dystrophy | Macular Degeneration | Lymphoma, Follicular | Stickler Syndrome | Miyoshi Myopathy | Cystinuria | Exostoses | Early Infantile Epileptic Encephalopathy | Guanidinoacetate Methyltransferase Deficiency | Hyperkeratosis | Pigment Dispersion Syndrome | Renal Dysplasia | Glioblastoma | Sickle Cell Anemia | Beckwith-Wiedemann Syndrome | Aneurysm, Thoracic Aortic | Mountain Sickness | Spondyloepimetaphyseal Dysplasia With Joint Laxity, Type 3 | Brachial Plexus Neuropathy | Zollinger-Ellison Syndrome | Lewy Body Dementia | Renal Hypomagnesemia 3 | Dwarfism | Precocious Puberty | Poikiloderma With Neutropenia | Short-chain Acyl-CoA Dehydrogenase Deficiency | Scapuloperoneal Myopathy, X-linked Dominant | Anodontia | Fibrosarcoma | Abetalipoproteinemia | Keratopathy | Lennox-Gastaut Syndrome | Rotor Syndrome | Scoliosis | Glycogen Storage Disease Type 1b | Harlequin Ichthyosis | Metabolic Syndrome | Basal Ganglia Cerebrovascular Disease | Globozoospermia | Demyelinating Diseases | Poretti-Boltshauser Syndrome | Waldenstrom Macroglobulinemia | Oral Lichen Planus | Tetraplegia | Clouston Hidrotic Ectodermal Dysplasia | NGLY1 Deficiency | Episodic Ataxia | Anemia | Necrobiosis Lipoidica | Essential Fructosuria | Lichen Planus | Toxoplasmosis | Ileitis | Epilepsy Of Infancy With Migrating Focal Seizures | Antisocial Personality Disorder | Small Lymphocytic Lymphoma | Myoclonic Epilepsy With Ragged Red Fibers | Deafness, Dystonia, And Cerebral Hypomyelination | Dysmorphophobia | Acute Myeloid Leukemia | Avian Influenza | Coloboma | Mitochondrial DNA Depletion Syndrome, Encephalomyopathic Form | Diastrophic Dysplasia | Progressive Osseous Heteroplasia | Familial Isolated Hyperparathyroidism | Waardenburg Syndrome Type 2 | Spinocerebellar Ataxia Type 7 | Hypercholesterolemia, Familial | Chronic Beryllium Disease | Rett Syndrome | Vitiligo | Argininosuccinic Aciduria | Macular Corneal Dystrophy Type 1 | Polycythemia Vera | Zellweger Syndrome | Shprintzen-Goldberg Syndrome | Kaposi Sarcoma | Psoriasis | Intestinal Tuberculosis | Focal Segmental Glomerulosclerosis | Hyperkalemic Periodic Paralysis | Menetrier Disease | Dent Disease | Schistosomiasis | Papilledema | Aicardi-Goutieres Syndrome | Gaucher Disease | Endometrial Hyperplasia | Rhizomelic Chondrodysplasia Punctata | Multiple Congenital Anomalies-hypotonia-seizures Syndrome 2 | Ehlers-Danlos Syndrome With Progressive Kyphoscoliosis, Myopathy, And Hearing Loss | Myasthenia Gravis | Acute Motor Axonal Neuropathy | Infertility, Male | Thalassemia | Pancreatitis, Chronic | Sarcoidosis | Tyrosine Hydroxylase Deficiency | Otosclerosis | Otopalatodigital Syndrome Type 2 | Spinocerebellar Ataxia Type 16 | Nephrocalcinosis | Spinocerebellar Ataxia Type 5 | Bainbridge-Ropers Syndrome | Erectile Dysfunction | Adrenal Insufficiency | Endometriosis | Wilson's Disease | Lymphedema | Osteogenesis Imperfecta Type III | Hypolipoproteinemia | Hepatic Adenomatosis | CDKL5 Deficiency Disorder | Neurodevelopmental Disorder With Central Hypotonia And Dysmorphic Facies | Keloid | Familial Episodic Pain Syndrome | Waardenburg Syndrome Type 4 | Gestational Trophoblastic Disease | Fibronectin Glomerulopathy | Diffuse Palmoplantar Keratoderma | Tuberculosis | Seborrheic Dermatitis | Pseudomyxoma Peritonei | Wiskott-Aldrich Syndrome | Angiosarcoma Of The Breast | Noonan Syndrome | Nephrotic Syndrome | Persistent Fetal Circulation | Personality Disorders | Non-bullous Congenital Ichthyosiform Erythroderma | Histiocytosis | Ichthyosis | Spinal Muscular Atrophy | Bruck Syndrome | Hypereosinophilic Syndrome | Goldenhar Syndrome | Azoospermia | Pulverulent Zonular Cataract | Isobutyryl-CoA Dehydrogenase Deficiency | Neuroma | Anti-glomerular Basement Membrane Disease | Autoimmune Polyendocrinopathy Syndrome Type I | Trachoma | Kidney Stones | Osteochondroma | Sickle Cell Disease | Charcot-Marie-Tooth Disease | Xeroderma Pigmentosum Variant Type | Alexander Disease | Brooke-Spiegler Syndrome | Episodic Ataxia Type 1 | Dystonia | Glanzmann Thrombasthenia | Werner's Syndrome | Sertoli Cell-only Syndrome | Incontinentia Pigmenti | Paternal Uniparental Disomy Of Chromosome 14 | Osteogenesis Imperfecta Type VI | Hypotrichosis, Congenital, With Juvenile Macular Dystrophy | Ganglioglioma | Usher Syndrome Type IIC | Still Disease | Pouchitis | Creatine Deficiency Syndrome Due To AGAT Deficiency | Monilethrix | Fibrosis | Cancer, Prostate | Congenital Fiber-type Disproportion Myopathy | Pneumonia, Bacterial | Restless Legs Syndrome | Presbyopia | Hypertension, Essential | Prediabetes | Thyroiditis | Meningococcal Infections | Familial Pheochromocytoma-paraganglioma | VACTERL Association | Sleep Apnea | Granuloma Annulare | Pierre Robin Syndrome | Peyronie's Disease | Raynaud Phenomenon | Japanese Encephalitis | Arterial Tortuosity Syndrome | Connective Tissue Disorders | Huntington's Disease-like 2 | Glioblastoma Multiforme | Pseudohypoparathyroidism Type 2 | Liebenberg Syndrome | Polyomavirus Nephropathy | Dyggve-Melchior-Clausen Disease | Thrombosis | Waardenburg Syndrome Type 2E | Primary Lateral Sclerosis | Corneal Neovascularization | Ehlers-Danlos Syndrome | Lymphoma, Mantle Cell | Keratoconus | Charcot-Marie-Tooth Disease Type 2T | Hereditary Inclusion Body Myopathy | Cancer, Brain | Spinocerebellar Ataxia Type 21 | Guillain-Barre Syndrome | Tremor | Schistosomiasis Mansoni | Desmosterolosis | Sensorineural Hearing Loss | Double Outlet Right Ventricle | Evans Syndrome | Spinal Muscular Atrophy Type 3 | Cerebrovascular Disorders | Leber Congenital Amaurosis | Hyperprolactinemia | Melanoma, Malignant | Gray Platelet Syndrome | Congenital Hypofibrinogenemia | Eclampsia | Trichothiodystrophy | Low Tension Glaucoma | Histoplasmosis | Smith-Kingsmore Syndrome | Congenital Dyserythropoietic Anemia Type 4 | Cholestasis | Hypophosphatasia | Left Ventricular Noncompaction | Anal Fissure | Myeloid Leukemia | Lymphoma, Primary Cutaneous Anaplastic Large Cell | Lissencephaly 2 | Blood Protein Disorders | Kashin-Beck Disease | Bloom Syndrome | Epidermodysplasia Verruciformis | Idiopathic Multicentric Castleman Disease | Usher Syndrome | Diabetes Insipidus | Hypokalemia | Mohr-Tranebjaerg Syndrome | Hepatitis, Autoimmune | Cancer, Breast | Polycystic Liver | Hodgkin Lymphoma | Jaundice, Obstructive | Multiple Sclerosis | Echinococcosis | Trichotillomania | Progressive Encephalopathy-optic Atrophy Syndrome | Goiter, Nodular | Ectodermal Dysplasia | Hypervalinemia | Early Infantile Epileptic Encephalopathy 4 | PHARC Syndrome | Hypertension, Portal | Frank-ter Haar Syndrome | Corneal Ulcer | Purpura, Thrombotic Thrombocytopenic | Lymphoproliferative Disease, X-linked | Periodontitis | HANAC Syndrome | Congenital Lipoid Adrenal Hyperplasia | Creutzfeldt-Jakob Disease | Myositis | Hyperparathyroidism-jaw Tumor Syndrome | Vitamin K Deficiency | Congenital Adrenal Hyperplasia 1 | Tyrosinemia | Corneal Dystrophy | Congenital Myasthenic Syndrome | Multicystic Renal Dysplasia | Juvenile Xanthogranuloma | Giant Cell Arteritis | Common Variable Immunodeficiency | Chronic Myeloid Leukemia | Brugada Syndrome 1 | Platyspondylic Lethal Skeletal Dysplasia, Torrance Type | Erythema Multiforme | Vestibular Disease | Nutrition Disorders | Congenital Torticollis | Sick Sinus Syndrome | Amenorrhea | Pseudohypoaldosteronism | Granular Corneal Dystrophy Type 1 | Waardenburg Syndrome Type 2A | Scleritis | Cholecystitis | Shwachman-Bodian-Diamond Syndrome | Chloridorrhea, Congenital | Inborn Errors Of Metabolism | Cirrhosis | Spastic Paraplegia Type 7 | Congenital Dyserythropoietic Anemia | Huntington's Disease | Cataract | Lymphopenia | Arteriosclerosis | Cancer, Colon | Micro Syndrome | Renal Tubular Acidosis | Rubeosis Iridis | Congenital Afibrinogenemia | Keratosis, Seborrheic | Blepharo-cheilo-odontic Syndrome | Neuropathy | Myocardial Infarction | Cardiospondylocarpofacial Syndrome