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

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

Ichthyosis, X-linked | Encephalitis | Megacystis-microcolon-intestinal Hypoperistalsis Syndrome | Atopy | Neurofibroma | Methylmalonic Aciduria And Homocystinuria, CblC Type | Trichomegaly | Marfan Syndrome | DICER1 Syndrome | Tylosis With Esophageal Cancer | Charcot-Marie-Tooth Disease, Type 1A | Pure Red Cell Aplasia | Agranulocytosis | Ulcerative Colitis | NDH Syndrome | Heart Block | Bladder Exstrophy | Epidermolysis Bullosa Acquisita | Crisponi Syndrome | Atelosteogenesis Type 2 | Mucolipidosis Type III | Schwannoma | Meleda Disease | McLeod Syndrome | Bethlem Myopathy | Sarcomatoid Carcinoma Of The Lung | Astigmatism | Frank-ter Haar Syndrome | Schaaf-Yang Syndrome | Medium-chain Acyl-CoA Dehydrogenase Deficiency | Heterotaxy | ACTH-independent Macronodular Adrenal Hyperplasia | Acral Lentiginous Melanoma | Obesity | McKusick Type Metaphyseal Chondrodysplasia | Chediak-Higashi Syndrome | Pituitary Disorders | Lafora Disease | Granuloma Annulare | Epithelioid Hemangioma | Lymphoma, AIDS-related | Central Pain Syndrome | Seborrheic Dermatitis | Brugada Syndrome 1 | Combined Pituitary Hormone Deficiency | Richter's Syndrome | Neurocutaneous Syndromes | Knobloch Syndrome | HELLP Syndrome | X-linked Sideroblastic Anemia | Mannosidase Deficiency Diseases | Aphasia | Hypermetropia | Impulse Control Disorder | Cancer, Bladder | Multicystic Renal Dysplasia | Endophthalmitis | Chylothorax, Congenital | Spitz Nevus | Chronic Lymphocytic Leukemia | Episodic Ataxia | Hepatitis D | Iron Metabolism Disorders | Meckel-Gruber Syndrome | Juvenile Hyaline Fibromatosis | Acute Generalized Exanthematous Pustulosis | Cluster Headache | Hyperparathyroidism-jaw Tumor Syndrome | Pulmonary Alveolar Microlithiasis | Anorectal Fistula | Ichthyosis Hystrix, Curth-Macklin Type | Spasticity | Azoospermia | Sulfite Oxidase Deficiency | Anovulation | Vertebrobasilar Insufficiency | Poirier-Bienvenu Neurodevelopmental Syndrome | Nail-Patella Syndrome | Microtia | Leukemia | Long QT Syndrome Type 3 | Hereditary Multiple Exostoses | Papilledema | Stroke, Hemorrhagic | Hemophilia | Encephalopathy, Glycine | Hypogonadism | Scabies | Polycystic Kidney, Autosomal Dominant | Influenza | Hyperphenylalaninemia | Bronchiectasis | Multiple Epiphyseal Dysplasia | Pierpont Syndrome | Glycogen Storage Disease Type 1 | Meningococcal Infections | Communication Disorders | Cholangiocarcinoma | Dementia, Vascular | Triple A Syndrome | Stickler Syndrome | Van Der Knaap Disease | Kleine-Levin Syndrome | Pulmonary Tuberculosis | Cat Eye Syndrome | Charcot-Marie-Tooth Disease Type 2T | Omenn Syndrome | Chromosome 9q34.3 Deletion Syndrome | Thalassemia | Pregnancy, Ectopic | Long QT Syndrome Type 2 | Metaphyseal Chondrodysplasia, Schmid Type | Meningioma | Cellulitis | Pierson Syndrome | Chronic Myeloid Leukemia | Glycogen Storage Disease Type 5 | Mast Cell Leukemia | Systemic Mastocytosis | Pseudohypoparathyroidism Type 1B | Oculocutaneous Albinism | Jacobsen Syndrome | Lennox-Gastaut Syndrome | C3 Glomerulopathy | Alazami Syndrome | Lymphoma, B-cell | Neurocutaneous Melanocytosis | Cholesteryl Ester Storage Disease | Gliosarcoma | Seizures | Cutaneous T-cell Lymphoma | Encephalopathy, Ethylmalonic | Biotinidase Deficiency | Autosomal Recessive Spastic Paraplegia Type 35 | Periventricular Nodular Heterotopia | Cushing Syndrome | Cryptosporidiosis | Intracranial Hypertension | Retinopathy, Diabetic | Anthrax | Antisocial Personality Disorder | Peritonitis | Neuromyelitis Optica | Thanatophoric Dysplasia Type 1 | Niemann-Pick Disease, Type C | Granular Corneal Dystrophy Type 1 | Bardet-Biedl Syndrome | Disseminated Intravascular Coagulation | Panuveitis | Osteoarthritis | Kawasaki Disease | Cutaneous Lupus Erythematosus | DOCK8 Immunodeficiency Syndrome | Cohen Syndrome | Parapsoriasis | Sick Sinus Syndrome 1 | Histiocytosis | Spinocerebellar Ataxia Type 23 | Demyelinating Diseases | Aspartylglycosaminuria | Insulinoma | Amyotrophic Lateral Sclerosis, Juvenile | Congenital Diaphragmatic Hernia | Avian Influenza | Cardiac Arrest | Microphthalmia | Esotropia | Parvovirus B19 Infection | Methylmalonic Acidemia | Smith-Lemli-Opitz Syndrome | Barrett Esophagus | Retinopathy Of Prematurity | Myelomeningocele | Intestinal Pseudo-obstruction | Oligoasthenoteratozoospermia | Leukoplakia | Intermittent Claudication | Congestive Heart Failure | Corneal Ulcer | Scapuloperoneal Spinal Muscular Atrophy | Spinocerebellar Ataxia Type 12 | Primary Carnitine Deficiency | Leber Hereditary Optic Neuropathy | Behavioral Variant Of Frontotemporal Dementia | Charcot-Marie-Tooth Disease Type 4D | Cholelithiasis | Fahr Disease | Meniere's Disease | Lentigo | Pterygium | Metachondromatosis | Hepatitis C, Chronic | Angioimmunoblastic T-cell Lymphoma | Tendinitis | Pneumonia, Mycoplasma | Hereditary Mixed Polyposis Syndrome | Blepharitis | Hereditary Folate Malabsorption | C3 Glomerulonephritis | Migraine | Pneumoconiosis | Spermatocele | Borderline Personality Disorder | GATA2 Deficiency | Neuroendocrine Cancer | Ocular Albinism Type 1 | Adenocarcinoma | Basan Syndrome | Congenital Dysfibrinogenemia | Precocious Puberty | Retinal Telangiectasia | Microvillus Inclusion Disease | Intracerebral Hemorrhage | Reflex Epilepsy | Cantu Syndrome | Vitiligo | Thrombocytopenia | Chordoma | Esophageal Carcinoma | Mucolipidosis | Prader-Willi Syndrome | Rift Valley Fever | Bone Marrow Necrosis | Smoldering Myeloma | Urea Cycle Disorder | Multiple Sclerosis, Chronic Progressive | Majeed Syndrome | Schamberg Disease | Sitosterolemia | Dementia | Oral Lichen Planus | Craniometaphyseal Dysplasia | Congenital Dyserythropoietic Anemia Type 1 | Autosomal Recessive Congenital Ichthyosis | Argininosuccinic Aciduria | Adenylosuccinate Lyase Deficiency | Leiomyosarcoma | Lymphedema-distichiasis Syndrome | Guanidinoacetate Methyltransferase Deficiency | Diffuse Palmoplantar Keratoderma | Obsessive-compulsive Disorder | Oculocutaneous Albinism Type 1 | Glycogen Storage Disease Type 1a | Open-angle Glaucoma | Connective Tissue Disorders | Hypersensitivity | Achromatopsia | Neurofibromatosis Type 1 | Retinitis Pigmentosa | Lyme Disease | Premenstrual Syndrome | Calcium Pyrophosphate Deposition Disease | Craniosynostosis | Becker Muscular Dystrophy | Vertigo | Carey-Fineman-Ziter Syndrome | WAGR Syndrome | Aplasia Cutis Congenita | Paternal Uniparental Disomy Of Chromosome 14 | Metatropic Dysplasia | Spondyloperipheral Dysplasia | Adenoma, Villous | Whipple's Disease | Postpoliomyelitis Syndrome | AIDS Dementia Complex | Renal Dysplasia | Giant Cell Glioblastoma | Acute Lung Injury | Mesothelioma, Malignant | Arthritis, Psoriatic | Primary Pigmented Nodular Adrenocortical Disease | Robinow Syndrome | Thyroiditis, Autoimmune | Eosinophilia | Spondylocarpotarsal Synostosis Syndrome | Nager Acrofacial Dysostosis | Addison Disease | Congenital Torticollis | Schizotypal Personality Disorder | Atrioventricular Septal Defect | Facioscapulohumeral Muscular Dystrophy Type 1 | Muir-Torre Syndrome | Inflammatory Bowel Disease | Meningioma, Benign | Paracoccidioidomycosis | Hepatitis | Riboflavin Transporter Deficiency Neuronopathy | Retinoschisis | Chondrodysplasia Punctata 1, X-linked Recessive | Sjogren Syndrome | Pearson Syndrome | Epidermodysplasia Verruciformis | Hemolytic Anemia | Aldosteronism | Encephalocele | Burn-McKeown Syndrome | Hypobetalipoproteinemias | Autism Spectrum Disorders | Mountain Sickness | Blepharospasm | Osteosclerosis | Chronic Leukemia | Chromosome 16p11.2 Deletion Syndrome | Dominant Optic Atrophy | 3-hydroxy-3-methylglutaric Aciduria | Neuroectodermal Tumors, Primitive | Spinal Muscular Atrophy | Spinocerebellar Ataxia Type 2 | Osteogenesis Imperfecta Type IV | Xeroderma Pigmentosum | Acute Motor Axonal Neuropathy | Hyperinsulinism-hyperammonemia Syndrome | Miyoshi Myopathy | Roberts Syndrome | Chondroma | Headache | Neonatal Progeroid Syndrome | Hemangioblastoma | Metabolic Diseases | Macular Degeneration | Necrobiosis Lipoidica | Keratosis, Actinic | Multisystemic Smooth Muscle Dysfunction Syndrome | Erdheim-Chester Disease | Aromatic L-amino Acid Decarboxylase Deficiency | Lichen Planus | Porphyria, Acute Intermittent | Distal Myopathy | Pachyonychia Congenita | Norrie Disease | Sleep Disorder | Frontotemporal Dementia | POEMS Syndrome | Hypotrichosis Simplex | Hemochromatosis | Primary Sclerosing Cholangitis | Early Infantile Epileptic Encephalopathy | Sarcosinemia | Hypertension, Pulmonary | Cockayne Syndrome | Craniopharyngioma | Hyperlipidemia, Familial Combined | Amish Infantile Epilepsy Syndrome | Progressive Osseous Heteroplasia | Chronic Myelomonocytic Leukemia | Primary Torsion Dystonia | Currarino Syndrome | 3-methylglutaconic Aciduria | AIDS | HANAC Syndrome | Esophagitis, Eosinophilic | Methemoglobinemia | Schwartz-Jampel-Aberfeld Syndrome | Pseudohypoparathyroidism Type 1A | Cataract | Orthostatic Intolerance | Basal Ganglia Disease | Multiple Hamartoma Syndrome | Spinocerebellar Ataxia Type 28 | Paroxysmal Nocturnal Hemoglobinuria | Polymyalgia Rheumatica | Agammaglobulinemia | Feingold Syndrome | Centronuclear Myopathy | Spondylocostal Dysostosis | Bernard-Soulier Syndrome | Yellow Fever | Adenomyosis | Mixed Connective Tissue Disease | Atherosclerosis | Adenoma, Pleomorphic | Ichthyosis Bullosa Of Siemens | Metabolic Syndrome | Uremic Pruritus | Cancer, Brain | Ganglioglioma | Cystitis | Xeroderma Pigmentosum Variant Type | Usher Syndrome Type III | Arts Syndrome | Cerebrovascular Disorders | Partington Syndrome | Porphyria Cutanea Tarda | Optic Neuropathy, Anterior Ischemic | Astrocytoma | Lipoma | Keratoconus | Myelofibrosis | Hyperinsulinemic Hypoglycemia | Keratosis | Lupus Erythematosus | Combined Malonic And Methylmalonic Acidemia | COACH Syndrome | Agnathia-Otocephaly Complex | Optic Nerve Diseases | Cancer, Breast | Castleman Disease | Budd-Chiari Syndrome | Charcot-Marie-Tooth Disease Type 4 | Speech Disorders