Disease

Congenital Torticollis

About the Disease
Congenital Torticollis, also known as congenital muscular torticollis, is related to contractures, congenital, torticollis, and malignant hyperthermia and torticollis, keloids, cryptorchidism, and renal dysplasia. The drugs Ropivacaine and Fentanyl have been mentioned in the context of this disorder. Affiliated tissues include spinal cord, trachea and tongue.

Common Targets
CACNA1A

疾病靶点研报
Congenital Torticollis

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

Other Diseases

Renal Tubular Acidosis | Ocular Surface Squamous Neoplasia | Hyperandrogenemia | Antiphospholipid Syndrome | Primary Hyperoxaluria Type 1 | Malonyl-CoA Decarboxylase Deficiency | Focal Dermal Hypoplasia | Tendinopathy | Hypercalciuria | Van Der Knaap Disease | Lipid Metabolism Disorders | Brugada Syndrome 1 | Hyperphenylalaninemia | Multiple Sclerosis, Primary Progressive | Mitochondrial DNA Depletion Syndrome 13 | Spinocerebellar Ataxia Type 5 | Alpers Syndrome | Iron Metabolism Disorders | Angioimmunoblastic T-cell Lymphoma | Pfeiffer Syndrome | Vitamin A Deficiency | Pathological Gambling | McLeod Syndrome | Neurodevelopmental Disorder With Central Hypotonia And Dysmorphic Facies | Plasmacytoma | Persistent Fetal Circulation | Osteogenesis Imperfecta Type V | Odonto-onycho-dermal Dysplasia | Ameloblastoma | Pneumococcal Meningitis | Splenomegaly | Spondylocostal Dysostosis | Primary Biliary Cholangitis | Melanocytic Nevus | Myoclonic Epilepsy With Ragged Red Fibers | Urea Cycle Disorder | Epidermolytic Ichthyosis, Annular | Holt-Oram Syndrome | VACTERL Association | Hypopituitarism | Common Variable Immunodeficiency | Syndactyly | FG Syndrome | Pseudohypoaldosteronism | Angioedema | Pemphigus | Tonsillitis | Pseudo-pseudohypoparathyroidism | Neuropathy | Cystinuria | CEDNIK Syndrome | Pulmonary Alveolar Microlithiasis | Alveolar Capillary Dysplasia | Vitiligo | Ectopia Lentis, Isolated, Autosomal Recessive | Dengue Shock Syndrome | Seizures | Marinesco-Sjogren Syndrome | Albinism | Hypertrophic Osteoarthropathy, Primary, Autosomal Recessive 2 | Sarcoma, Ewing | Coenzyme Q10 Deficiency | Amyotrophic Lateral Sclerosis-parkinsonism-dementia Complex | Craniolenticulosutural Dysplasia | Open-angle Glaucoma | Anencephaly | Mucolipidosis Type III | Lactose Intolerance | Keloid | Acute Generalized Exanthematous Pustulosis | Pachyonychia Congenita | Uveitis, Anterior | Osteoarthritis | Blue Nevus | Hemophilia | Peeling Skin Syndrome Type B | Epithelial-myoepithelial Carcinoma | C3 Glomerulopathy | Vertebrobasilar Insufficiency | Alopecia | Melnick-Needles Syndrome | Usher Syndrome Type I | Micro Syndrome | Cerebral Cavernous Malformations | Diabetes Mellitus, Transient Neonatal | Congenital Myasthenic Syndrome | Spermatocele | Hyperthermia, Malignant | Whipple's Disease | Histiocytosis | Cheilitis | Meningioma | Campomelic Dysplasia | Hereditary Coproporphyria | Steel Syndrome | Oral Lichen Planus | Osteogenesis Imperfecta Type IV | Paraplegia | Dystrophy, Cone-rod | Trichotillomania | Pulmonary Tuberculosis | Diffuse Idiopathic Pulmonary Neuroendocrine Cell Hyperplasia | Lymphopenia | Atelosteogenesis Type 1 | Phenylketonuria II | Corneal Edema | Bardet-Biedl Syndrome | Pemphigus Foliaceus | Acromesomelic Dysplasia | Pulmonary Alveolar Proteinosis | Myofibromatosis | Rolandic Epilepsy | Dyslipidemia | Ventricular Septal Defect | Adenoma, Pleomorphic | Multiple Epiphyseal Dysplasia | Congenital Tufting Enteropathy | Speech Disorders | Tinea | Fukuyama Congenital Muscular Dystrophy | Crohn's Disease | Astrocytoma | Charcot-Marie-Tooth Disease, Type 2C | Branchiootorenal Syndrome | Vertigo | Congenital Ichthyosiform Erythroderma | Tendinitis | Low Phospholipid Associated Cholelithiasis | Sporadic Hemiplegic Migraine | Thromboembolism | Pyruvate Kinase Deficiency | Retinoblastoma | Platelet Disorders | Hyperglycemia | Prurigo Nodularis | DRESS Syndrome | Thyroid Dyshormonogenesis | Cerebrotendinous Xanthomatosis | Benign Hereditary Chorea | Hypogonadism | Scleritis | Trichorhinophalangeal Syndrome | Polydactyly | Trigonocephaly | Neuroblastoma | Cirrhosis | Ebstein Anomaly | Hepatoblastoma | Esotropia | Hypotrichosis | Graft-versus-host Disease | Mannosidase Deficiency Diseases | Amelanotic Melanoma | Myotonia | Waardenburg Syndrome Type 2 | Kabuki Syndrome 2 | Sweet Syndrome | Blepharo-cheilo-odontic Syndrome | Epidermolysis Bullosa Simplex, Generalized | Kidney Stones | Hypothyroidism | Androgen Insensitivity | DiGeorge Syndrome | Glycogen Storage Disease Type 1b | Hypersensitivity | Uremic Pruritus | Hypothalamic Obesity | Rickets | Thymoma, Malignant | Hyperlipidemia, Familial Combined | Chylomicron Retention Disease | Eating Disorder | Gerodermia Osteodysplastica | Exostoses | Hereditary Sensory Neuropathy Type 1 | Stevens-Johnson Syndrome | Anuria | Hartsfield Syndrome | Dementia | Esophageal Carcinoma | Glaucomatocyclitic Crisis | Majeed Syndrome | Familial Episodic Pain Syndrome | Kernicterus | Charcot-Marie-Tooth Disease Type 4 | Melanoma | Snyder-Robinson Syndrome | Bursitis | Macrophage Activation Syndrome | Neovascular Glaucoma | Nephroblastoma | Pre-eclampsia | Diabetes Insipidus, Nephrogenic | Learning Disability | Mandibuloacral Dysplasia With Type A Lipodystrophy | Brenner Tumor | Porokeratosis | Neutropenia | Gitelman Syndrome | Spondylo-ocular Syndrome | Sialidosis Type I | Viral Meningitis | Spinocerebellar Ataxia Type 38 | Restrictive Dermopathy | Zollinger-Ellison Syndrome | Esthesioneuroblastoma | Congenital Muscular Dystrophy | Disseminated Superficial Actinic Porokeratosis | Glaucoma, Congenital | Myelodysplasia | Metabolic Syndrome | Keratosis | WAGR Syndrome | Neurofibroma, Plexiform | Encephalopathy, Glycine | SAPHO Syndrome | Fuchs Dystrophy | Glycogen Storage Disease Type 1a | Leprosy | Pseudomyxoma Peritonei | Glomerulonephritis | 3-methylcrotonyl-CoA Carboxylase Deficiency | Deafness, Dystonia, And Cerebral Hypomyelination | Cryptosporidiosis | Meckel-Gruber Syndrome | Atopic Dermatitis | Diabetes Type 1 | Porphyria | Sjogren Syndrome | Cutaneous Angiosarcoma | Potocki-Shaffer Syndrome | Primary Hyperoxaluria Type 3 | Trichomegaly | Hypokalemia | Posterior Polar Cataract | Impulse Control Disorder | Dysthymia | Obsessive-compulsive Disorder | Spinocerebellar Ataxia Type 12 | Eiken Syndrome | Mitochondrial Myopathy | Adult Polyglucosan Body Disease | Giant Axonal Neuropathy | COACH Syndrome | Amyloidosis | Myopia | Arts Syndrome | Chronic Mucocutaneous Candidiasis | Mumps | CREST Syndrome | Autonomic Neuropathy | PASLI Disease | Leukoencephalopathy, Progressive Multifocal | Inborn Errors Of Metabolism | Benign Familial Neonatal Convulsions | Retinoschisis | Mast Cell Leukemia | Endometriosis | Congenital Aniridia | Transcobalamin Deficiency | Bacterial Meningitis | Lipid Storage Diseases | Anti-NMDA Receptor Encephalitis | Language Disorders | Microtia | Hydrolethalus Syndrome | Acute Myeloid Leukemia | GM2-gangliosidosis AB Variant | Hidradenitis Suppurativa | Antithrombin III Deficiency | Glucagonoma | Echinococcosis | Parkinson's Disease | Encephalocele | Myotonic Disorders | Sickle Cell Anemia | Colitis, Microscopic | Ichthyosis | Citrullinemia | Abetalipoproteinemia | Parkinsonism | Roberts Syndrome | Autonomic Nervous System Disorders | Cholestasis | Donnai-Barrow Syndrome | Woodhouse-Sakati Syndrome | Platyspondylic Lethal Skeletal Dysplasia, Torrance Type | Facioscapulohumeral Muscular Dystrophy Type 1 | Weill-Marchesani Syndrome | Erythematotelangiectatic Rosacea | Keratitis-ichthyosis-deafness Syndrome | Pierre Robin Syndrome | Combined Pituitary Hormone Deficiency | Schizophrenia | Neurocysticercosis | Carotid Artery Disease | Waardenburg Syndrome Type 4A | Familial Hemiplegic Migraine | Agoraphobia | Familial Mediterranean Fever | Larsen Syndrome | Charcot-Marie-Tooth Disease Axonal Type 2N | Blastomycosis | Chiari Malformation Type I | Vascular Calcification | Proctitis | Pseudoachondroplasia | Overactive Bladder | Obesity, Morbid | Miyoshi Myopathy | Leiomyoma | Benign Familial Pemphigus | Chromosome 16p11.2 Deletion Syndrome | Colitis | Liver Failure | Gingivitis | Hereditary Xerocytosis | Proximal Symphalangism | Mitochondrial DNA Depletion Syndrome, Myopathic Form | Hypokalemic Periodic Paralysis | Pontocerebellar Hypoplasia Type 7 | Reflex Epilepsy | Renpenning Syndrome | Kaposi Sarcoma | Chorea | 3-hydroxy-3-methylglutaryl-CoA Synthase Deficiency | Intestinal Tuberculosis | Tularemia | Neuroleptic Malignant Syndrome | Smith-Magenis Syndrome | Hypotrichosis Simplex | Microcephaly, Seizures, And Developmental Delay | Long QT Syndrome Type 2 | Kleine-Levin Syndrome | Wieacker-Wolff Syndrome | Herpes Genitalis | Ichthyosis Hystrix, Curth-Macklin Type | Pemphigoid | Rothmund-Thomson Syndrome | Charcot-Marie-Tooth Disease Type 2E | Muir-Torre Syndrome | Lymphoma, Mantle Cell | Anorectal Fistula | Hereditary Hemorrhagic Telangiectasia Type 2 | Raynaud Phenomenon | Waardenburg Syndrome Type 1 | Cardiac Arrest | Carney-Stratakis Syndrome | Aicardi-Goutieres Syndrome | Hepatitis E | Klippel-Feil Syndrome | Seborrheic Dermatitis | Porphyria, Acute Intermittent | Lymphoma, AIDS-related | Spondyloepiphyseal Dysplasia Tarda, X-linked | Glycogen Storage Disease Type 0 | Herpes Simplex Dermatitis | Pilomatrix Carcinoma | Galloway-Mowat Syndrome | Familial Dysautonomia | Rhabdoid Tumor | Pulverulent Zonular Cataract | Erectile Dysfunction | Seasonal Mood Disorder | Glioma | Sleep Disorder | Juvenile Hyaline Fibromatosis | Pendred Syndrome | Cervicitis | Brachydactyly | Nephropathy | Schuurs-Hoeijmakers Syndrome | KBG Syndrome | Keratosis, Actinic | Acromegaly | Retinitis Pigmentosa | Thanatophoric Dysplasia Type 1 | Cancer, Bladder | Infantile Liver Failure Syndrome 1 | Corneal Dystrophy And Perceptive Deafness | Amblyopia | Histiocytic Sarcoma | Hepatitis A | Familial Isolated Hyperparathyroidism | Tyrosinemia | Veno-occlusive Disease | Tricho-hepato-enteric Syndrome | Gilbert Syndrome | Spinal And Bulbar Muscular Atrophy | Schizoaffective Disorder | Meesmann Corneal Dystrophy | Craniometaphyseal Dysplasia | Spinal Muscular Atrophy | Tay-Sachs Disease | Spinocerebellar Ataxia Type 15 | Pneumonia, Mycoplasma | Varices | Pituitary Dwarfism | Sick Sinus Syndrome | Familial Retinal Arterial Macroaneurysm