Disease

Emery-Dreifuss Muscular Dystrophy

About the Disease
Emery-Dreifuss Muscular Dystrophy, also known as edmd, is related to x-linked emery-dreifuss muscular dystrophy and emery-dreifuss muscular dystrophy 7, autosomal dominant. An important gene associated with Emery-Dreifuss Muscular Dystrophy is EMD (Emerin), and among its related pathways/superpathways are "Cell Cycle, Mitotic" and Separation of Sister Chromatids. The drugs D-Lysine and Anesthetics, Local have been mentioned in the context of this disorder. Affiliated tissues include heart, skeletal muscle and adipocyte, and related phenotypes are joint stiffness and myotonia

Common Targets
MAP2K1 | SYNE2 | SUN2 | SUN1 | TMPO | FHL1 | MAP2K2 | LMNA | SYNE1 | MYH7 | EMD

疾病靶点研报
Emery-Dreifuss Muscular Dystrophy

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

Other Diseases

Uveitis, Anterior | Takotsubo Cardiomyopathy | Endocarditis | Vasculitis | Tuberculous Meningitis | Ischemia | HELLP Syndrome | Multiple Epiphyseal Dysplasia | Vestibular Disease | Hypohidrotic Ectodermal Dysplasia | Amelanotic Melanoma | Meleda Disease | Familial Thoracic Aortic Aneurysm | Pseudoachondroplasia | Paraplegia | Purpura | Anorchia | Tendinitis | Osteomyelitis | Monilethrix | Blastoma, Pleuropulmonary | Diabetic Encephalopathy | Pathological Gambling | Spinocerebellar Ataxia | Peyronie's Disease | Fetal Akinesia Deformation Sequence | Ocular Surface Squamous Neoplasia | Colitis | Primary Hyperoxaluria Type 3 | Focal Facial Dermal Dysplasia | Inflammatory Myopathy | Epiphyseal Chondrodysplasia, Miura Type | Ependymoma | Fanconi Syndrome | Urticaria | Persistent Hyperplastic Primary Vitreous | Greenberg Dysplasia | C3 Glomerulonephritis | Osteogenesis Imperfecta Type II | Waardenburg Syndrome Type 2E | 3-hydroxy-3-methylglutaric Aciduria | Neuromyotonia | Hepatitis C, Chronic | Acute Lymphocytic Leukemia | Familial Pheochromocytoma-paraganglioma | Thalassemia, Beta | Genee-Wiedemann Syndrome | Waardenburg Syndrome Type 2A | Dowling-Degos Disease | Ocular Albinism Type 1 | Glycogen Storage Disease Type 0, Muscle | Chronic Enteropathy Associated With SLCO2A1 Gene | Adenoma, Villous | Swine Influenza | Pneumococcal Meningitis | Proximal Symphalangism | Anorectal Fistula | Dermatomyositis | Heroin Dependence | Nicotine Dependence | Adenosine Deaminase 2 Deficiency | Crigler-Najjar Syndrome | Epidermolysis Bullosa Simplex, Dowling-Meara Type | Dengue Hemorrhagic Fever | Paraganglioma | Desmosterolosis | Diabetic Nephropathy | Cluster Headache | Histoplasmosis | Bartsocas-Papas Syndrome | Blue Nevus | Pseudohypoparathyroidism Type 2 | Hepatic Steatosis | 17-beta-hydroxysteroid Dehydrogenase X Deficiency | Mitochondrial DNA Depletion Syndrome | Cornelia De Lange Syndrome | Chronic Kidney Disease | Acute Myeloid Leukemia | Neurofibromatosis Type 1 | Metatropic Dysplasia | Disseminated Intravascular Coagulation | Congenital Hypofibrinogenemia | Tricho-hepato-enteric Syndrome | Ehlers-Danlos Syndrome With Progressive Kyphoscoliosis, Myopathy, And Hearing Loss | Chondroma | Diamond-Blackfan Anemia | Congenital Hemolytic Anemia | Pericarditis | Cohen Syndrome | Epidermolysis Bullosa Acquisita | Echinococcosis | Aneurysm, Abdominal Aortic | Pontocerebellar Hypoplasia Type 7 | Albinism | Myocarditis | Lipid Storage Myopathy | Schaaf-Yang Syndrome | Myelomeningocele | Bursitis | Poikiloderma With Neutropenia | Ichthyosis Hystrix, Curth-Macklin Type | Familial Hemiplegic Migraine | Renal Tubular Acidosis | Esophageal Adenocarcinoma | Fibrillation, Atrial | Rhabdomyosarcoma, Alveolar | Lymphoma | Miyoshi Myopathy | Silicosis | Psoriasis | Leukodystrophies | Colon Adenoma | Photosensitivity | Teratozoospermia | Tenosynovial Giant Cell Tumor | Van Der Knaap Disease | Myoclonic Epilepsy With Ragged Red Fibers | Hemochromatosis | Avian Influenza | Aldosterone Deficiency | Esotropia | Gastric Atrophy | Succinic Semialdehyde Dehydrogenase Deficiency | Primary Cutaneous Amyloidosis | Achromatopsia | Anti-NMDA Receptor Encephalitis | Polycythemia | Leukocyte Adhesion Deficiency | Agoraphobia | Schwannoma | PHARC Syndrome | Myhre Syndrome | Hypermethioninemia | Alopecia Areata | Lymphoma, Primary Cutaneous Anaplastic Large Cell | Hemochromatosis Type 2 | Schwartz-Jampel-Aberfeld Syndrome | Wolman Disease | Non-Hodgkin Lymphoma | Ovarian Sex Cord-stromal Tumor | COACH Syndrome | Enlarged Vestibular Aqueduct | Localized Scleroderma | Dementia, Vascular | Krabbe Disease | Ichthyosis Bullosa Of Siemens | Nutrition Disorders | Chudley-McCullough Syndrome | Hereditary Folate Malabsorption | Hyperlipidemia Type V | Sickle Cell Disease | Ataxia-ocular Apraxia 2 | Sarcosinemia | Corneal Ulcer | Osteoporosis, Postmenopausal | Carey-Fineman-Ziter Syndrome | Carpal Tunnel Syndrome | Cholecystitis | Acrodermatitis | Obsessive-compulsive Disorder | Achondrogenesis | Congenital Mirror Movements | Spinocerebellar Ataxia Type 40 | Niemann-Pick Disease, Type A | Pontocerebellar Hypoplasia | Retinoschisis | Autonomic Neuropathy | Primary Biliary Cholangitis | Melanoma | Lipoma | Benign Familial Infantile Seizures | Glaucomatocyclitic Crisis | Atherosclerosis | Bruck Syndrome | Depression | Behavioral Variant Of Frontotemporal Dementia | Meckel-Gruber Syndrome | Renal Medullary Carcinoma | Colitis, Lymphocytic | Alpha-mannosidosis | Gnathodiaphyseal Dysplasia | Nevus | Intestinal Hypomagnesemia 1 | Anodontia | Congenital Afibrinogenemia | Congenital Disorders Of Glycosylation | Cat Eye Syndrome | Schizotypal Personality Disorder | Hyperbilirubinemia | Plasma Cell Leukemia | Hemoglobinopathies | Lennox-Gastaut Syndrome | Plasma Cell Dyscrasia | Diabetes Insipidus, Nephrogenic | Usher Syndrome Type III | Metanephric Adenoma | Acanthosis Nigricans | Autism | Cardiofaciocutaneous Syndrome | Optic Neuropathy | Spinocerebellar Ataxia Type 5 | Turner's Syndrome | Klippel-Feil Syndrome | Spina Bifida | Retinal Detachment | Steel Syndrome | Schizoaffective Disorder | Leri Pleonosteosis | Keloid | Hypersomnia | Microcephaly | Tremor | Parkinson Disease 6, Autosomal Recessive Early-onset | Crouzon Syndrome With Acanthosis Nigricans | Ganglioneuroma | Hyperkalemic Periodic Paralysis | Proteus Syndrome | Waardenburg Syndrome | Epidermolysis Bullosa Simplex | Porokeratosis | Pulmonary Tuberculosis | Portal Vein Thrombosis | Lichen Planus | Splenomegaly | X-linked Charcot-Marie-Tooth Disease | Glutaric Aciduria Type 2 | Sialoadenitis | Early Infantile Epileptic Encephalopathy 1 | DiGeorge Syndrome | Diffuse Mesangial Sclerosis | Liver Failure | Hypereosinophilic Syndrome | Sarcoma, Endometrial Stromal | Carney-Stratakis Syndrome | Mohr-Tranebjaerg Syndrome | Dermatofibrosarcoma | Hypotonia-cystinuria Syndrome | Tatton-Brown-Rahman Syndrome | Short-chain Acyl-CoA Dehydrogenase Deficiency | Sick Sinus Syndrome 1 | Spinocerebellar Ataxia Type 17 | Schnyder Crystalline Corneal Dystrophy | Stromal Corneal Dystrophy | Multiple Hamartoma Syndrome | Malaria | Multiple Sclerosis | Down Syndrome | Aspartylglycosaminuria | Rosacea | Spinocerebellar Ataxia Type 23 | Neurofibrosarcoma | Bethlem Myopathy | Persistent Mullerian Duct Syndrome | Cryoglobulinemia | Amyotrophic Lateral Sclerosis-parkinsonism-dementia Complex | Hyper IgE Syndrome | Idiopathic Multicentric Castleman Disease | Hypertriglyceridemia | Congenital Lipoid Adrenal Hyperplasia | Homocystinuria | Pure Autonomic Failure | Hypohidrotic Ectodermal Dysplasia, X-linked | Saethre-Chotzen Syndrome | Tinea | Adenoid Cystic Carcinoma | Epilepsy | Sepiapterin Reductase Deficiency | Cerebrovascular Disorders | High Molecular Weight Kininogen Deficiency | Exotropia | Spinal Muscular Atrophy | Lymphoproliferative Disorders | Neuromuscular Disorders | PASLI Disease | Familial Exudative Vitreoretinopathy | Aneurysm, Thoracic Aortic | Focal Dermal Hypoplasia | Prader-Willi Syndrome | Basal Cell Nevus Syndrome | 3-methylcrotonyl-CoA Carboxylase Deficiency | Mitochondrial Cytopathy | Posterior Polar Cataract | Primrose Syndrome | Pituitary Dwarfism | Lysosomal Acid Lipase Deficiency | Pseudo-pseudohypoparathyroidism | Meningococcal Meningitis | Primary Hyperoxaluria | Unverricht-Lundborg Syndrome | Multiple Sclerosis, Relapsing-remitting | Fatty Aldehyde Dehydrogenase Deficiency | Cardiac Sarcoidosis | Fundus Albipunctatus | Aromatic L-amino Acid Decarboxylase Deficiency | Scleroderma | Amelogenesis Imperfecta | Neurofibromatosis Type 2 | Long QT Syndrome Type 1 | ACTH-independent Macronodular Adrenal Hyperplasia | Retinal Dystrophy | Macular Degeneration | Ebstein Anomaly | Retinal Telangiectasia | Congenital Poikiloderma | Guttate Psoriasis | Infantile Neuroaxonal Dystrophy | Encephalopathy, Ethylmalonic | Polymicrogyria | Isovaleric Acidemia | Synovitis | Clouston Hidrotic Ectodermal Dysplasia | Osteoarthritis | Congenital Hereditary Endothelial Dystrophy Type I | Brenner Tumor | Lateral Meningocele Syndrome | Leukemia-lymphoma, Adult T-cell | Chondrosarcoma | Fukuyama Congenital Muscular Dystrophy | Thyroiditis | Craniofrontonasal Syndrome | Kabuki Syndrome 2 | Ectodermal Dysplasia | Juvenile Xanthogranuloma | Sorsby Fundus Dystrophy | Sarcoidosis, Pulmonary | Uremia | Cataract | Specific Granule Deficiency | Polycystic Kidney, Autosomal Recessive | Leber Congenital Amaurosis | Tetraplegia | Coronary Artery Disease | Membranous Nephropathy | Erythematotelangiectatic Rosacea | Epilepsy Of Infancy With Migrating Focal Seizures | Neurofibroma | Microphthalmia | Rolandic Epilepsy | Intermittent Claudication | Congenital Adrenal Hyperplasia 1 | Charcot-Marie-Tooth Disease, Type 2C | Schizophrenia | Juvenile Myoclonic Epilepsy | Prolactinoma | Pendred Syndrome | Malignant Peripheral Nerve Sheath Tumor | Papilledema | MIRAGE Syndrome | Goiter, Nodular | Autoimmune Polyendocrinopathy Syndrome Type I | Burn-McKeown Syndrome | Blepharitis | Hepatitis, Autoimmune | Evans Syndrome | Sensorineural Hearing Loss | Amenorrhea | Lymphoma, Mantle Cell | Carcinoma, Merkel Cell | Schnitzler Syndrome | Extramammary Paget's Disease | Polycythemia Vera | Follicular Dendritic Cell Sarcoma | Chediak-Higashi Syndrome | Pulmonary Stenosis | Familial Dysautonomia | Nephrocalcinosis | Otitis Externa | Spinocerebellar Ataxia Type 1 | Robinow Syndrome | Craniolenticulosutural Dysplasia | Familial Retinal Arterial Macroaneurysm | Lewy Body Dementia | Colorectal Adenoma | Presbyopia | Shock, Cardiogenic | Transcobalamin Deficiency | Hypertrophic Osteoarthropathy, Primary, Autosomal Recessive 1 | Leukoencephalopathy, Progressive Multifocal | Congenital Dyserythropoietic Anemia Type 4 | Pneumoconiosis | Osmotic Demyelination Syndrome | Trichorhinophalangeal Syndrome | Periventricular Nodular Heterotopia | Birt-Hogg-Dube Syndrome | Trichomegaly | Osteogenesis Imperfecta Type IV | Early Infantile Epileptic Encephalopathy 13 | Macrophagic Myofasciitis | Nephrotic Syndrome Type 1 | Syndactyly | Hartnup Disease | Osteogenesis Imperfecta Type I | Neurodegeneration Due To Cerebral Folate Transport Deficiency | Paget's Disease Of The Breast | Progressive Familial Intrahepatic Cholestasis Type 3 | Whipple's Disease | Renal-hepatic-pancreatic Dysplasia | Premenstrual Syndrome | Li-Fraumeni Syndrome | Periodic Limb Movement Disorder