Neuromuscular Disorders

About the Disease
Neuromuscular Disease, also known as neuromuscular diseases, is related to emery-dreifuss muscular dystrophy and central core disease of muscle, and has symptoms including athetosis, back pain and headache. An important gene associated with Neuromuscular Disease is RYR1 (Ryanodine Receptor 1), and among its related pathways/superpathways are Cardiac conduction and Cytoskeletal Signaling. The drugs Vaccines and Immunologic Factors have been mentioned in the context of this disorder. Affiliated tissues include skeletal muscle, bone marrow and spinal cord, and related phenotypes are muscle and homeostasis/metabolism

Common Targets
SGCG | G367 | MPV17 | SCN8A | CYTB | SLC25A46 | HPGD | KY | ASCC1 | ACVR1B | SPEG | Potassium Channels (nonspecified subtype) | VCP | ATP6 | COX20 | MSTN | COL6A3 | MSTO1 | TNFSF4 | CNR1 | CD40LG | TFRC | VWA1 | SGCB | SH3TC2 | DYSF

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

Other Diseases

Sarcomatoid Carcinoma Of The Lung | Congenital Primary Aphakia | Macrodactyly | Thyroiditis | Colitis, Collagenous | Focal Segmental Glomerulosclerosis | Huntington's Disease | Neural Tube Defect | Hydronephrosis | Glutaric Aciduria Type 1 | Cholestasis | Glaucoma | Acute Lymphocytic Leukemia | Erythrokeratodermia Variabilis | Pityriasis Rubra Pilaris | Congenital Generalized Lipodystrophy | Kohlschutter-Tonz Syndrome | Lymphedema | Periodic Limb Movement Disorder | Osteogenesis Imperfecta Type II | Allan-Herndon-Dudley Syndrome | Cutaneous T-cell Lymphoma | Keratoconjunctivitis | Graft-versus-host Disease | Skin Fragility-woolly Hair Syndrome | Aldosteronism | Neurodevelopmental Disorders | Aromatic L-amino Acid Decarboxylase Deficiency | Primary Sclerosing Cholangitis | Diabetes Insipidus, Nephrogenic | Temtamy Preaxial Brachydactyly Syndrome | Cancer, Colon | Hyperthyroidism | Vertigo | Motor Neuron Diseases | Sezary Syndrome | Congenital Dyserythropoietic Anemia Type 1 | Prune Belly Syndrome | Cataract | Fetal Alcohol Syndrome | Spinal Muscular Atrophy Type 3 | Sick Sinus Syndrome 1 | Harlequin Ichthyosis | Usher Syndrome Type II | Pulverulent Zonular Cataract | Proctitis | Veno-occlusive Disease | Addison Disease | Polyradiculopathy | Congenital Heart Defects | Achromatopsia | Cancer, Prostate | Alveolar Capillary Dysplasia | Mitochondrial DNA Depletion Syndrome 13 | Neurofibromatosis-Noonan Syndrome | Pendred Syndrome | Charcot-Marie-Tooth Disease Type 2D | Fuchs Dystrophy | Porphyria Cutanea Tarda | 3-M Syndrome | Smith-Lemli-Opitz Syndrome | Asplenia | Antisynthetase Syndrome | Autosomal Recessive Spastic Paraplegia Type 75 | Meningococcal Meningitis | Extramammary Paget's Disease | Miyoshi Myopathy | Pyelonephritis | Schwannoma | Hypermethioninemia | Hypertrophic Osteoarthropathy, Primary, Autosomal Recessive 2 | Holt-Oram Syndrome | Persistent Mullerian Duct Syndrome | Spinocerebellar Ataxia Type 15 | Gastroenteritis | Primrose Syndrome | Epicondylitis | Multisystemic Smooth Muscle Dysfunction Syndrome | Megacystis-microcolon-intestinal Hypoperistalsis Syndrome | Sengers Syndrome | Multiple Congenital Anomalies-hypotonia-seizures Syndrome 2 | Muscular Dystrophy | Chorea | Dysferlinopathy | Diabetes Gestational | Aspartylglycosaminuria | Familial Retinal Arterial Macroaneurysm | Congenital Dyserythropoietic Anemia | Bronchiolitis | Osteogenesis Imperfecta | Hyperuricemic Nephropathy, Familial Juvenile | Pneumonia, Bacterial | Sclerocornea | Anencephaly | Frontotemporal Dementia With Amyotrophic Lateral Sclerosis | Spinocerebellar Ataxia Type 12 | B-cell Chronic Lymphocytic Leukemia | C3 Glomerulonephritis | Leprosy | Retinitis Pigmentosa 3 | Pineoblastoma | Inflammatory Myopathy | Retinal Vasculitis | Porphyria, Variegate | Specific Granule Deficiency | Trichothiodystrophy | Perivascular Epithelioid Cell Tumor | Ectrodactyly | Mastitis | Farber Disease | Paraganglioma, Carotid Body | Episodic Ataxia Type 1 | Neurodevelopmental Disorder With Central Hypotonia And Dysmorphic Facies | Glutaric Aciduria Type 3 | Adenomatoid Tumor | Swine Influenza | Pheochromocytoma | Feingold Syndrome | Meningeal Melanocytoma | Anovulation | Spondylo-ocular Syndrome | Endometriosis | DOCK8 Immunodeficiency Syndrome | Myhre Syndrome | Compartment Syndrome | Charcot-Marie-Tooth Disease, Type 1A | Cutis Laxa | Tuberculosis | Pemphigus | Osteosclerosis | Congenital Aniridia | Pierpont Syndrome | Uremia | Leiomyoma | Hepatitis, Chronic | Diarrhea | Fatty Aldehyde Dehydrogenase Deficiency | Ichthyosis, X-linked | Spinocerebellar Ataxia Type 14 | Ocular Surface Squamous Neoplasia | Wagner Disease | Corneal Dystrophies, Hereditary | Usher Syndrome Type IIC | Chronic Myeloid Leukemia | Stargardt Disease | Marinesco-Sjogren Syndrome | Chylomicron Retention Disease | Non-Hodgkin Lymphoma | Loeys-Dietz Syndrome Type 4 | Anorectal Fistula | Plasmacytoma | Angioedema, Hereditary | Cholangiocarcinoma | Neuroleptic Malignant Syndrome | ICF Syndrome | Congenital Myopathy | Familial Mediterranean Fever | Hyperparathyroidism, Secondary | Chudley-McCullough Syndrome | Chronic Idiopathic Myelofibrosis | Yellow Fever | Arterial Tortuosity Syndrome | Acute Tubular Necrosis | Hyperparathyroidism | Astrocytoma, Anaplastic | Lymphoma, Primary Cutaneous Anaplastic Large Cell | Combined Pituitary Hormone Deficiency | Okihiro Syndrome | Cerebrotendinous Xanthomatosis | Hyper IgE Syndrome | Diffuse Palmoplantar Keratoderma | Neurocysticercosis | Systemic Mastocytosis | Spondyloperipheral Dysplasia | Nager Acrofacial Dysostosis | Wilson's Disease | Colitis, Microscopic | Azoospermia | Spinocerebellar Ataxia | Adrenoleukodystrophy, X-linked | Usher Syndrome Type I | Schnyder Crystalline Corneal Dystrophy | Immunoproliferative Disorders | Diabetic Nephropathy | Porphyria | Carcinoma, Small Cell | Proteasome-associated Autoinflammatory Syndrome 2 | CHOPS Syndrome | Galloway-Mowat Syndrome | Demyelinating Diseases | Wiskott-Aldrich Syndrome | Dysplastic Nevus | Chronic Thromboembolic Pulmonary Hypertension | Congenital Ichthyosiform Erythroderma | Coma | Progressive Familial Intrahepatic Cholestasis Type 2 | Microcephalic Osteodysplastic Primordial Dwarfism, Type I | Lymphangioma | Silicosis | Chronic Neutrophilic Leukemia | Hereditary Spherocytosis | Herpes Genitalis | Pericarditis | 17-beta-hydroxysteroid Dehydrogenase X Deficiency | Kabuki Syndrome | Sialidosis | Epidermal Nevus Syndrome | Osmotic Demyelination Syndrome | Scapuloperoneal Spinal Muscular Atrophy | Hyperparathyroidism-jaw Tumor Syndrome | Spinocerebellar Ataxia Type 2 | Non-small Cell Lung Cancer | Central Core Disease | Pure Autonomic Failure | Cholelithiasis | Parkinsonism | Lymphoma, B-cell | Gastritis | Early Infantile Epileptic Encephalopathy 13 | GAPO Syndrome | DRESS Syndrome | Marfan Syndrome | Oculocutaneous Albinism Type 1 | Intracerebral Hemorrhage | Intracranial Hypertension | Hepatitis | Prurigo Nodularis | Neuroectodermal Tumors, Primitive | Agoraphobia | Sporadic Inclusion Body Myositis | Fowler's Syndrome | Pompe Disease | Amelanotic Melanoma | Bardet-Biedl Syndrome | Leishmaniasis, Cutaneous | Obesity, Morbid | Meconium Ileus | Glycogen Storage Disease Type 1a | Oculocutaneous Albinism Type 4 | Fahr Disease | Eating Disorder | Botulism | Conjunctivitis, Allergic | Spondyloepimetaphyseal Dysplasia With Joint Laxity, Type 3 | Cushing Syndrome | Pseudohypoparathyroidism Type 1B | Tyrosinemia | 3-hydroxyacyl-CoA Dehydrogenase Deficiency | Auriculocondylar Syndrome | Parkinson Disease 6, Autosomal Recessive Early-onset | Acne | Polycystic Kidney, Autosomal Recessive | Lymphoma, Follicular | VACTERL Association | Olmsted Syndrome | Tyrosinemia Type 2 | Vulvovaginitis | Pterygium | Aneurysm, Abdominal Aortic | Potocki-Shaffer Syndrome | Sclerosteosis 2 | Pneumonia, Viral | Early Infantile Epileptic Encephalopathy | Chromosome 17q21.31 Deletion Syndrome | Acral Lentiginous Melanoma | Optic Nerve Hypoplasia, Bilateral | CDKL5 Deficiency Disorder | Hypophosphatemic Rickets With Hypercalciuria, Hereditary | Tangier Disease | Primary Pigmented Nodular Adrenocortical Disease | Pfeiffer Syndrome | Dyggve-Melchior-Clausen Disease | Castleman Disease | Costello Syndrome | Rotor Syndrome | Acquired Partial Lipodystrophy | Dentinogenesis Imperfecta | Hypohidrotic Ectodermal Dysplasia, X-linked | Vogt-Koyanagi-Harada Syndrome | Spinocerebellar Ataxia Type 38 | Blue Rubber Bleb Nevus Syndrome | Colitis | Gynecomastia | IgA Deficiency | ADNP Syndrome | Lymphoma Lymphoblastic | Nicolaides-Baraitser Syndrome | Diabetic Encephalopathy | Nijmegen Breakage Syndrome | Kleine-Levin Syndrome | Beta-Propeller Protein-associated Neurodegeneration | Exostoses | Cabezas Syndrome | Dermatofibrosarcoma | Early Infantile Epileptic Encephalopathy 28 | Nevus | Spinal Cord Diseases | Whipple's Disease | Empyema | Gingivitis | Delayed Sleep Phase Syndrome | GATA2 Deficiency | Albinism | Gestational Trophoblastic Disease | Coffin-Lowry Syndrome | HELLP Syndrome | Melanoma, Uveal | Autosomal Recessive Congenital Ichthyosis | Metabolic Syndrome | Leukemia-lymphoma, Adult T-cell | Hyperinsulinemic Hypoglycemia | Peeling Skin Syndrome Type B | Pemphigoid | Diabetes Mellitus, Transient Neonatal | Retinoblastoma | Cavitary Optic Disc Anomalies | Perry Syndrome | Gerstmann-Straussler-Scheinker Syndrome | Pupil Disorders | Muscle Wasting | Uremic Pruritus | Esophageal Adenocarcinoma | Adrenomyeloneuropathy | Triple A Syndrome | Hartnup Disease | Leukoencephalopathy, Progressive Multifocal | Neurofibromatosis Type 2 | Cerebral Amyloid Angiopathy | Abetalipoproteinemia | Thyroiditis, Autoimmune | Restless Legs Syndrome | Transthyretin-related Amyloidosis | Bulimia Nervosa | Hypotrichosis, Congenital, With Juvenile Macular Dystrophy | Basal Ganglia Disease, Biotin-responsive | Cri-du-chat Syndrome | Glycogen Storage Disease Type 0, Muscle | MELAS Syndrome | Brugada Syndrome 1 | Nephrotic Syndrome Type 1 | Neurotoxicity | Carotid Artery Disease | Microcephaly | Left Ventricular Noncompaction | Arthropathy | Autoimmune Disease | Erythropoietic Protoporphyria | Pituitary Dwarfism | Keratosis | Superficial Spreading Melanoma | Neuropathy | Chordoma | Diabetes | Congenital Afibrinogenemia | Benign Familial Pemphigus | Majeed Syndrome | Graves Disease | Acrodermatitis Enteropathica | Odonto-onycho-dermal Dysplasia | Enhanced S-cone Syndrome | Eosinophilic Asthma | Liver Failure | Biotinidase Deficiency | Sjogren Syndrome | Dementia | Tracheal Disorders | Bone Giant Cell Tumor | Progressive Familial Intrahepatic Cholestasis Type 1 | Gardner Syndrome | Mountain Sickness | McCune-Albright Syndrome | Kernicterus | Porencephaly | Alstrom Syndrome | Trichuriasis | Subacute Sclerosing Panencephalitis | Polyomavirus Nephropathy | Sarcoidosis, Pulmonary | Multiple Sclerosis, Secondary Progressive | Dystrophy, Cone-rod | Hernia, Inguinal | Spasticity | Epidermolysis Bullosa Simplex, Dowling-Meara Type | Corneal Dystrophy And Perceptive Deafness | Scoliosis | Intestinal Tuberculosis | Amelogenesis Imperfecta | Rheumatoid Arthritis | Marshall-Smith Syndrome | Mitochondrial Disease | Neurofibromatosis | Craniofacial Dysostosis | DEND Syndrome | Carbonic Anhydrase VA Deficiency | Combined Deficiency Of Factor V And Factor VIII | Vici Syndrome | Angiosarcoma | Conn Syndrome | Autonomic Neuropathy | Panic Disorder