Congenital Myopathy

About the Disease
Batten-Turner Congenital Myopathy, also known as congenital myopathy, is related to myopathy, congenital, bailey-bloch and king-denborough syndrome. An important gene associated with Batten-Turner Congenital Myopathy is MYH7 (Myosin Heavy Chain 7), and among its related pathways/superpathways are Cardiac conduction and DREAM Repression and Dynorphin Expression. The drugs Lamotrigine and Mexiletine have been mentioned in the context of this disorder. Affiliated tissues include skeletal muscle, eye and brain, and related phenotypes are myopathy and abnormality of the nervous system

Common Targets
RYR1 | FXR1 | Cyclophilins (nonspecified subtype) | TNNC2 | TRIP4 | SPEG | TTN | MYOF | CFAP410 | BAG3

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

Other Diseases

Neuroma | Geleophysic Dysplasia | Tylosis With Esophageal Cancer | Nestor-Guillermo Progeria Syndrome | Spermatocele | Malignant Fibrous Histiocytoma | Cartilage Disorders | Neutrophilia | Cancer, Kidney | Gerodermia Osteodysplastica | Leukoplakia, Oral | Erdheim-Chester Disease | Granular Corneal Dystrophy Type 1 | Central Retinal Artery Occlusion | Crimean-Congo Hemorrhagic Fever | Corneal Neovascularization | Roberts Syndrome | Spinocerebellar Ataxia Type 8 | Polyneuropathy | Epidermolysis Bullosa Simplex, Generalized | Keratitis-ichthyosis-deafness Syndrome | Prurigo Nodularis | Schamberg Disease | Charcot-Marie-Tooth Disease, Type 2C | Interstitial Lung Diseases | Sorsby Fundus Dystrophy | Methemoglobinemia Type IV | Pontocerebellar Hypoplasia Type 2 | Hyperparathyroidism, Primary | Endocarditis | Cri-du-chat Syndrome | Cholesteryl Ester Storage Disease | Placenta Previa | Li-Fraumeni Syndrome | Avellino Corneal Dystrophy | Encephalitis | Ataxia-hypogonadism-choroidal Dystrophy Syndrome | Blue Rubber Bleb Nevus Syndrome | Kaposi Sarcoma | Tetanus | Osteochondrosis | Cancer, Prostate | Necrotizing Autoimmune Myopathy | Progressive Familial Intrahepatic Cholestasis Type 1 | Veno-occlusive Disease | Poretti-Boltshauser Syndrome | Nephronophthisis | Idiopathic Multicentric Castleman Disease | Diabetic Nephropathy | Usher Syndrome Type II | Patent Ductus Arteriosus | Hydrocephalus, Normal Pressure | Hyperphosphatasia With Intellectual Disability Syndrome 4 | Hypercholesterolemia, Familial | Barrett Esophagus | Myofibromatosis | Kindler Syndrome | Brugada Syndrome 1 | Transcobalamin Deficiency | Senior-Loken Syndrome | Hepatic Veno-occlusive Disease | Menetrier Disease | Mitochondrial Encephalomyopathy | Encephalopathy, Glycine | Lymphoproliferative Disease, X-linked | Intellectual Disability, Autosomal Dominant 5 | Hypophosphatemic Rickets, Autosomal Recessive, 1 | Kallmann Syndrome | Keloid | Homocystinuria | Glioblastoma | Carcinoma, Signet Ring Cell | Proopiomelanocortin Deficiency | Intermittent Claudication | Acute Lung Injury | Hypocalcemia | Melanoma, Uveal | 3-methylglutaconic Aciduria Type IV | Gallstones | Hepatitis, Autoimmune | Primary Carnitine Deficiency | Enterocolitis, Necrotizing | Erythrokeratodermia Variabilis | Autoimmune Polyendocrine Syndrome | Behavioral Variant Of Frontotemporal Dementia | Neural Tube Defect | Infantile Neuroaxonal Dystrophy | Allan-Herndon-Dudley Syndrome | Alpha-mannosidosis | Congenital Bile Acid Synthesis Defect | Ehlers-Danlos Syndrome | TARP Syndrome | Craniometaphyseal Dysplasia | Schuurs-Hoeijmakers Syndrome | Alazami Syndrome | Sturge-Weber Syndrome | ADNP Syndrome | Babesiosis | Dominant Optic Atrophy | Oligodendroglioma | Brachydactyly | X-linked Myotubular Myopathy | Dementia, Vascular | Spinocerebellar Ataxia Type 17 | Scleritis | Hydrocephalus | Okihiro Syndrome | Argininosuccinic Aciduria | Spinocerebellar Ataxia Type 31 | Vasculitis | Pachyonychia Congenita | Macrodactyly | Mitochondrial DNA Depletion Syndrome, Encephalomyopathic Form | Skin Papilloma | Bleeding Disorder Due To CalDAG-GEFI Deficiency | Schistosomiasis Mansoni | Hypertension, Pulmonary | Fetal Alcohol Syndrome | Basal Ganglia Disease, Biotin-responsive | Hereditary Folate Malabsorption | Hyperlipidemia | Small Lymphocytic Lymphoma | Mosaic Variegated Aneuploidy Syndrome 2 | Thyrotoxic Periodic Paralysis | Nephrocalcinosis | Retinitis Pigmentosa 3 | Cold Agglutinin Disease | Inflammatory Myofibroblastic Tumor | Tinea Versicolor | Cantu Syndrome | Lafora Disease | Osteopathia Striata With Cranial Sclerosis | Premenstrual Syndrome | Generalized Epilepsy And Paroxysmal Dyskinesia | Erythema Nodosum | Varices | Myoclonic Atonic Epilepsy | Hydrolethalus Syndrome | Primary Hyperoxaluria Type 3 | Proteasome-associated Autoinflammatory Syndrome 2 | Scabies | Rheumatoid Arthritis | Hyperacusis | Diastrophic Dysplasia | Thrombocythemia, Essential | Seasonal Mood Disorder | Rash | Lattice Corneal Dystrophy Type 1 | Multiple Sclerosis, Secondary Progressive | Bartsocas-Papas Syndrome | Neurofibromatosis Type 1 | Encephalocele | Glycogen Storage Disease Type 6 | Antley-Bixler Syndrome | Gardner Syndrome | Hypervalinemia | Tangier Disease | Keratosis, Seborrheic | Leber Hereditary Optic Neuropathy | Still Disease | McKusick Type Metaphyseal Chondrodysplasia | Congenital Aniridia | Cranial Nerve Disease | Burn-McKeown Syndrome | Carcinoma, Transitional Cell | Urethritis | Early Infantile Epileptic Encephalopathy 4 | Amenorrhea | Familial Cerebral Amyloid Angiopathy | Esophageal Carcinoma | Sclerosteosis | Pseudohypoparathyroidism Type 1C | Hyperuricemia | Wieacker-Wolff Syndrome | Rhinitis | Seminoma | Alopecia Areata | Glycogen Storage Disease Type 3 | Phosphoenolpyruvate Carboxykinase Deficiency, Cytosolic | PASLI Disease | Spinocerebellar Ataxia Type 1 | Hypohidrotic Ectodermal Dysplasia | Panniculitis | Retinopathy, Diabetic | Sarcoma, Alveolar Soft Part | Osteoporosis | Osteochondroma | Deafness, Dystonia, And Cerebral Hypomyelination | Williams Syndrome | Occipital Neuralgia | Maple Syrup Urine Disease | Oguchi Disease-2 | Diarrhea | Spondylosis | Nanophthalmos | Spondyloepiphyseal Dysplasia Tarda, X-linked | Milk Allergy | Aplastic Anemia | B-cell Chronic Lymphocytic Leukemia | Oculocutaneous Albinism Type 1 | Bullous Pemphigoid | Syphilis | Kabuki Syndrome 2 | Cardiac Sarcoidosis | Amelanotic Melanoma | Sporadic Hemiplegic Migraine | Spondylocostal Dysostosis | Bartter Syndrome | T-cell Lymphoma, Subcutaneous Panniculitis-like | Hypoglycemia | Micro Syndrome | Smith-Lemli-Opitz Syndrome | Autoimmune Polyendocrinopathy Syndrome Type I | Epidermolytic Hyperkeratosis | Atherosclerosis | Vestibular Disease | Phenylketonuria II | Hyperoxaluria | Carotid Artery Disease | Chondrodysplasia Punctata 2, X-linked Dominant | Paroxysmal Kinesigenic Dyskinesia | Acrocallosal Syndrome | Epicondylitis | Waardenburg Syndrome Type 1 | Eiken Syndrome | Hypercalcemia | Vascular Calcification | Guanidinoacetate Methyltransferase Deficiency | Basal Cell Nevus Syndrome | Nemaline Myopathy 8 | Metabolic Diseases | Heterotaxy | Glycogen Storage Disease Type 1b | Melanocytic Nevus | Muscular Dystrophy | Dyggve-Melchior-Clausen Disease | Thyroid Dysgenesis | Glaucomatocyclitic Crisis | Sleep Apnea, Obstructive | Localized Scleroderma | Craniosynostosis | Triphalangeal Thumb-polysyndactyly Syndrome | Uveitis, Anterior | Rothmund-Thomson Syndrome | Hyperthyroidism | Primary Familial Brain Calcification | Acute Myeloid Leukemia | Compartment Syndrome | Medium-chain Acyl-CoA Dehydrogenase Deficiency | Mucolipidosis | Plasma Cell Leukemia | Knobloch Syndrome | Multicentric Carpotarsal Osteolysis Syndrome | Aldosteronism | Pycnodysostosis | Anencephaly | Turner's Syndrome | Aromatic L-amino Acid Decarboxylase Deficiency | HELLP Syndrome | Asthma, Nocturnal | Hereditary Elliptocytosis | Microcephalic Primordial Dwarfism | Cushing Syndrome | N-acetylglutamate Synthase Deficiency | Schnitzler Syndrome | Anodontia | Jalili Syndrome | Macrophage Activation Syndrome | Retinitis Pigmentosa | Multiple Sclerosis, Primary Progressive | Hereditary Spastic Paraplegia | Sarcoidosis, Pulmonary | Best Macular Dystrophy | Cramp Fasciculation Syndrome | Familial Male-limited Precocious Puberty | Dermatofibrosarcoma | Obesity, Morbid | Vitamin D Deficiency | Follicular Dendritic Cell Sarcoma | Potocki-Shaffer Syndrome | Skin Carcinoma | Cryopyrin-associated Periodic Syndromes | Pseudohermaphroditism | Measles | Wolff-Parkinson-White Syndrome | Aspartylglycosaminuria | Greenberg Dysplasia | Epidermolysis Bullosa Simplex With Mottled Pigmentation | Cardiomyopathy, Restrictive | Amish Infantile Epilepsy Syndrome | Diabetes Insipidus | Salla Disease | Papillon-Lefevre Syndrome | Congenital Sodium Diarrhea | Malaria | Multiple Sclerosis, Relapsing-remitting | Sandhoff Disease | Adrenoleukodystrophy, X-linked | Spinocerebellar Ataxia | Nicotine Addiction | Erythromelalgia | Myocarditis | Chronic Kidney Disease | Paraganglioma, Carotid Body | Epilepsy | Johanson-Blizzard Syndrome | Crisponi Syndrome | HUPRA Syndrome | Cholestasis, Intrahepatic | Hennekam Lymphangiectasia-lymphedema Syndrome | Cheilitis | Angiodysplasia | Contact Dermatitis | Myoclonus-dystonia Syndrome | Lipoma | Wilson's Disease | Stargardt Disease | Hypotension, Orthostatic | Acral Lentiginous Melanoma | Hyper IgE Syndrome | Plasma Cell Dyscrasia | Glioma | Lissencephaly 2 | Netherton Syndrome | Priapism | Otopalatodigital Syndrome Type 2 | Cholangitis | Pneumococcal Meningitis | Motor Neuron Diseases | Empyema | Lesch-Nyhan Syndrome | Pendred Syndrome | Acute Kidney Injury | Hyperinsulinemic Hypoglycemia | Vaginitis | Aicardi-Goutieres Syndrome | Rett Syndrome | Neurocysticercosis | Hyperinsulinemia | Ebstein Anomaly | Hepatitis B, Chronic | Leri Pleonosteosis | Chiari Malformation Type I | Filariasis | Histoplasmosis | Neurofibromatosis | Rickets | Trichorhinophalangeal Syndrome | Goldenhar Syndrome | Walker-Warburg Syndrome | Tibial Muscular Dystrophy | POEMS Syndrome | Barakat Syndrome | Diffuse Intrinsic Pontine Glioma | Coenzyme Q10 Deficiency | Costello Syndrome | Anti-NMDA Receptor Encephalitis | Agranulocytosis | LRBA Deficiency | Glucagonoma | Retinal Detachment | Silicosis | Sialidosis | Microcephaly, Seizures, And Developmental Delay | Non-small Cell Lung Cancer | Binge Eating Disorder | Chromosome 16p11.2 Deletion Syndrome | Retinal Telangiectasia | Pain | Tyrosinemia | Usher Syndrome Type IIC | Paracoccidioidomycosis | Gestational Trophoblastic Disease | Acute Anterior Uveitis | Chondroma | Infertility | Cryptorchidism | Hypertensive Retinopathy | Hepatorenal Syndrome | Spondylometaphyseal Dysplasia | Bruck Syndrome | Fanconi Anemia | Glioblastoma Multiforme | Postaxial Polydactyly | Wolfram Syndrome | Ichthyosis, X-linked | Charcot-Marie-Tooth Disease Type 4B1 | Varicocele | Hypogonadism | Rotor Syndrome | 3-hydroxyacyl-CoA Dehydrogenase Deficiency | Gnathodiaphyseal Dysplasia | Waardenburg Syndrome | Otitis Externa | Meningococcal Meningitis | Acute Chest Syndrome | Osteosclerosis | Schwartz-Jampel-Aberfeld Syndrome | Emery-Dreifuss Muscular Dystrophy | Gray Platelet Syndrome