Disease

Thrombotic Microangiopathy

About the Disease
Thrombotic Microangiopathy, also known as tma, is related to viral infectious disease and systemic lupus erythematosus. An important gene associated with Thrombotic Microangiopathy is CD46 (CD46 Molecule). The drugs Acetylcysteine and Ravulizumab have been mentioned in the context of this disorder. Affiliated tissues include endothelial, kidney and bone marrow.

Common Targets
HLA-E | CFI | ADAMTS13 | EGFL8 | CFHR1 | MASP2 | CFHR5 | PLG | CFHR3 | PRMT7 | Kallikrein (nonspecified subtype) | DGKE | C3 | F11 | CFH | SLC26A2 | APOL1 | MASP1 | G6PD | THBD | CFB | CD40LG | VWF | C5

疾病靶点研报
Thrombotic Microangiopathy

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

Other Diseases

Schwannoma | Hemangioma | Chorea | Ulcerative Colitis | Choriocarcinoma | Early Infantile Epileptic Encephalopathy 4 | Malnutrition | Pierson Syndrome | Liebenberg Syndrome | Myhre Syndrome | Ocular Hypertension | Epidermolytic Hyperkeratosis | Glycogen Storage Disease Type 1 | Sarcomatoid Carcinoma Of The Lung | Vitamin B12 Deficiency | Fraser Syndrome | Hereditary Hemorrhagic Telangiectasia Type 2 | Sarcoma | Fibrillation, Atrial | Schizoaffective Disorder | Hypertrophic Osteoarthropathy, Primary, Autosomal Recessive 1 | Creutzfeldt-Jakob Disease | Ependymoma | Thyrotoxic Periodic Paralysis | Liver Failure | 3-methylglutaconic Aciduria | Lichen Sclerosus | Hyperprolactinemia | Temtamy Preaxial Brachydactyly Syndrome | Giant Axonal Neuropathy | Carcinoma, Small Cell | Multiple Epiphyseal Dysplasia | Blastomycosis | Osteogenesis Imperfecta Type I | Behcet's Disease | Enlarged Vestibular Aqueduct | Erythropoietic Protoporphyria | Renal Failure | Hereditary Sensory Neuropathy Type 1 | Seminoma | Nestor-Guillermo Progeria Syndrome | Aldosterone Synthase Deficiency | Erythrokeratodermia Variabilis | Gray Platelet Syndrome | Paraplegia | Cervicitis | Vertebrobasilar Insufficiency | Lassa Fever | Diabetes Insipidus, Neurogenic | Periodic Limb Movement Disorder | Cockayne Syndrome | Impulse Control Disorder | Oguchi Disease-2 | Cold Agglutinin Disease | Hartsfield Syndrome | Renal Medullary Carcinoma | Schwartz-Jampel-Aberfeld Syndrome | Whipple's Disease | Coronary Heart Disease | Aplasia Cutis Congenita | Chronic Leukemia | Hypophosphatasia | Asthma, Exercise-induced | Bleeding Disorder Due To CalDAG-GEFI Deficiency | Chronic Mucocutaneous Candidiasis | Goldenhar Syndrome | Autism | Chudley-McCullough Syndrome | Autoimmune Autonomic Ganglionopathy | Cerebellofaciodental Syndrome | Enterocolitis, Necrotizing | Diabetes Mellitus, Transient Neonatal | Tyrosinemia Type 1 | Charcot-Marie-Tooth Disease Type 4D | Creatine Deficiency Syndrome | Charcot-Marie-Tooth Disease, Type 2C | WAGR Syndrome | Anti-NMDA Receptor Encephalitis | Malignant Fibrous Histiocytoma | Waardenburg Syndrome Type 2A | Spinocerebellar Ataxia Type 31 | Pyoderma Gangrenosum | Myopathy | Cholera | Ichthyosis | Spitz Nevus | Dysplastic Nevus | Thin Basement Membrane Disease | Platyspondylic Lethal Skeletal Dysplasia, Torrance Type | CEDNIK Syndrome | Schuurs-Hoeijmakers Syndrome | Pheochromocytoma | Infantile Liver Failure Syndrome 1 | Keratoconjunctivitis | Hyperostosis | Panic Disorder | Globozoospermia | Frontometaphyseal Dysplasia | Phenylketonuria II | Congenital Muscular Dystrophy | Shprintzen-Goldberg Syndrome | Hypertriglyceridemia | Dermatofibrosarcoma | Medulloblastoma | Spinocerebellar Ataxia Type 42 | Kallmann Syndrome | Sulfite Oxidase Deficiency | Ataxia-ocular Apraxia 2 | Myasthenia | Esotropia | Mumps | Double Outlet Right Ventricle | Bone Giant Cell Tumor | Coloboma | Gerstmann-Straussler-Scheinker Syndrome | Macular Corneal Dystrophy Type 1 | Toxoplasmosis | Spinocerebellar Ataxia Type 15 | Hypertension, Pulmonary | Mucolipidosis Type IV | Coffin-Siris Syndrome | Multiple Sclerosis, Secondary Progressive | Gyrate Atrophy Of The Choroid And Retina | Chronic Myelomonocytic Leukemia | Priapism | Lymphedema | Thalassemia | Hypermethioninemia | Ornithine Transcarbamylase Deficiency | Agammaglobulinemia | Glutaric Aciduria Type 3 | Farber Disease | Thanatophoric Dysplasia | Glycogen Storage Disease Type 9 | Lysosomal Acid Lipase Deficiency | Hernia, Inguinal | Sengers Syndrome | Apert Syndrome | Gnathodiaphyseal Dysplasia | 3-hydroxyacyl-CoA Dehydrogenase Deficiency | Encephalocele | Borjeson-Forssman-Lehmann Syndrome | Multiple Mitochondrial Dysfunctions Syndrome Type 1 | Thyroiditis, Autoimmune | Idiopathic Multicentric Castleman Disease | Basal Ganglia Cerebrovascular Disease | Hepatitis, Autoimmune | Greenberg Dysplasia | Malaria | Methemoglobinemia | Hyperthermia, Malignant | Fibronectin Glomerulopathy | Hypoplastic Left Heart Syndrome | Primary Cutaneous Amyloidosis | Familial Exudative Vitreoretinopathy | Papilledema | Carcinoma, Merkel Cell | Pericarditis | Hyperlipidemia | Polycythemia | Wiskott-Aldrich Syndrome | Batten Disease | Triphalangeal Thumb-polysyndactyly Syndrome | Sleep Apnea, Obstructive | Cardiomyopathy, Peripartum | Pulmonary Stenosis | Dystonia Musculorum Deformans | Chromosome 9q34.3 Deletion Syndrome | X-linked Acrogigantism | Desmosterolosis | Hereditary Sensory And Autonomic Neuropathy | Discoid Lupus Erythematosus | Atherosclerosis | Chondrodysplasia Punctata | DRESS Syndrome | Leukemia | Exostoses | Hyperkeratosis | Myocardial Infarction | Multiple Sclerosis, Primary Progressive | Non-small Cell Lung Cancer | Otitis Externa | Parkinson's Disease | Autosomal Recessive Bestrophinopathy | Xeroderma Pigmentosum | Focal Dermal Hypoplasia | Tyrosine Hydroxylase Deficiency | Omenn Syndrome | Pityriasis Rubra Pilaris | Progressive Familial Intrahepatic Cholestasis Type 2 | Episodic Ataxia | Deafness, Dystonia, And Cerebral Hypomyelination | VACTERL/VATER Association | Carcinoma In Situ | Primary Hyperoxaluria Type 1 | Teratozoospermia | Sarcoma, Ewing | Chordoid Glioma | Blau Syndrome | Episodic Ataxia Type 1 | Pigment Dispersion Syndrome | Photosensitivity | Hemophagocytic Lymphohistiocytosis | Corticobasal Syndrome | Epidermolysis Bullosa Simplex | Lymphedema-distichiasis Syndrome | Hodgkin Lymphoma | Autosomal Recessive Spastic Paraplegia Type 35 | Budd-Chiari Syndrome | Holoprosencephaly | Conduct Disorder | Gastric Atrophy | Chorea-acanthocytosis | Sickle Cell Anemia | Pregnancy, Ectopic | Androgen Insensitivity | Colitis | Esophagitis | Hennekam Lymphangiectasia-lymphedema Syndrome | Stromal Corneal Dystrophy | Paternal Uniparental Disomy Of Chromosome 14 | Lichen Planus | Calcium Pyrophosphate Deposition Disease | Addison Disease | Oculopharyngeal Muscular Dystrophy | Cystinuria | Microcephalic Osteodysplastic Primordial Dwarfism, Type II | Duodenal Atresia | Left Ventricular Noncompaction | Uveitis | Alzheimer Disease, Late Onset | 3-methylglutaconic Aciduria Type I | Cabezas Syndrome | Intellectual Disability, Autosomal Dominant 5 | Cholangiocarcinoma | Huntington's Disease | N-acetylglutamate Synthase Deficiency | Meleda Disease | Adenomyosis | Metachondromatosis | Sjogren Syndrome | Combined Deficiency Of Factor V And Factor VIII | Hyperuricemia | Peripheral Neuropathy | Wieacker-Wolff Syndrome | Cushing Syndrome | Trigonocephaly | Chronic Inflammatory Demyelinating Polyneuropathy | VACTERL Association | Disseminated Intravascular Coagulation | Oligoastrocytoma | Intracranial Hypertension | Pure Autonomic Failure | Aplastic Anemia | Hypercalcemia | Bursitis | Riboflavin Transporter Deficiency Neuronopathy | Molybdenum Cofactor Deficiency | Hypohidrotic Ectodermal Dysplasia | Keratitis-ichthyosis-deafness Syndrome | Arterial Tortuosity Syndrome | Cocaine-Related Disorders | Patent Foramen Ovale | Congenital Dyserythropoietic Anemia Type 1 | Tinea | B-cell Chronic Lymphocytic Leukemia | Blepharospasm | Hepatitis E | Branchiootorenal Syndrome | Goiter, Nodular | Bartter Syndrome | Encephalopathy, Hepatic | Eating Disorder | Frontotemporal Dementia With Amyotrophic Lateral Sclerosis | Spinal Muscular Atrophy With Progressive Myoclonic Epilepsy | Familial Thoracic Aortic Aneurysm | Hemosiderosis | Mitochondrial DNA Depletion Syndrome 13 | Bartsocas-Papas Syndrome | Spinal Cord Diseases | Cataplexy | Adenylosuccinate Lyase Deficiency | Hemochromatosis | Hypertensive Retinopathy | Papillorenal Syndrome | Cardiac Sarcoidosis | Long-chain 3-hydroxyacyl-coenzyme A Dehydrogenase Deficiency | Osteopathia Striata With Cranial Sclerosis | Ameloblastoma | Arthritis, Gouty | Mabry Syndrome | Hereditary Mixed Polyposis Syndrome | Enhanced S-cone Syndrome | Restless Legs Syndrome | Familial Glucocorticoid Deficiency | Cardiofaciocutaneous Syndrome | Hyperlipidemia Type V | Postpartum Depression | Distal Myopathy | Osteonecrosis | Basal Ganglia Disease | Achondrogenesis | Multiple Myeloma | Subacute Sclerosing Panencephalitis | Diabetic Nephropathy | Multiple Sclerosis, Chronic Progressive | Motor Neuron Diseases | Gangliosidosis | Porphyria | Spitzoid Melanoma | Parvovirus B19 Infection | Pseudohypoparathyroidism Type 1A | Myocarditis | Inflammatory Myofibroblastic Tumor | Neurocutaneous Melanocytosis | Metanephric Adenoma | Lung Diseases | Mast Cell Leukemia | Beta-Propeller Protein-associated Neurodegeneration | Chondroma | Cole-Carpenter Syndrome | Depression | Fibrosis | Nail Disorder, Nonsyndromic Congenital | Anorchia | Eczema | Presbycusis | Epidermolysis Bullosa Simplex, Localized | Rothmund-Thomson Syndrome | Emery-Dreifuss Muscular Dystrophy | Hyperparathyroidism, Secondary | Polymyalgia Rheumatica | Thrombophlebitis | Diabetic Encephalopathy | Waardenburg Syndrome Type 2E | Dyslipidemia | Still Disease | Tylosis With Esophageal Cancer | Hereditary Pyropoikilocytosis | Gliosarcoma | Phosphoglycerate Dehydrogenase Deficiency | Chloridorrhea, Congenital | Exocrine Pancreatic Insufficiency | Neurogenic Bladder | Prune Belly Syndrome | Neurofibromatosis Type 2 | Pituitary Stalk Interruption Syndrome | Diamond-Blackfan Anemia | Monilethrix | Progressive External Ophthalmoplegia | Botulism | 5-oxoprolinase Deficiency | Malaria, Cerebral | Spinocerebellar Ataxia Type 28 | Wolfram Syndrome 2 | Vaginitis | Osteomyelitis | Sepiapterin Reductase Deficiency | Intermittent Claudication | Sandhoff Disease | Limb Girdle Muscular Dystrophy | Retinopathy Of Prematurity | Hypocalcemia | Familial Mediterranean Fever | Rotor Syndrome | Interstitial Lung Diseases | Twin-to-twin Transfusion Syndrome | Spondylolisthesis | Diabetes Insipidus, Nephrogenic | Tetanus | Lymphoma, Primary Cutaneous Anaplastic Large Cell | Acanthosis Nigricans | Malonyl-CoA Decarboxylase Deficiency | Neuromyelitis Optica | Bloom Syndrome | Familial Dysautonomia | Olmsted Syndrome | Macrophagic Myofasciitis | Charcot-Marie-Tooth Disease Type 3 | Crimean-Congo Hemorrhagic Fever | Leukemia-lymphoma, Adult T-cell | Sitosterolemia | Hepatitis, Chronic | Chondrodysplasia Punctata 1, X-linked Recessive | Achromatopsia | Premenstrual Syndrome | Esophageal Motility Disorders | Hashimoto Thyroiditis | Ectodermal Dysplasia | Polycystic Kidney, Autosomal Dominant | Spinocerebellar Ataxia Type 2 | Cousin Syndrome | Pupil Disorders | Infantile Refsum Disease | Tendinitis | H Syndrome | Dementia, Vascular | Diabetic Neuropathy | Gingivitis | Pemphigus