Myelitis

About the Disease
Myelitis, also known as spinal cord inflammation nos, is related to schistosomiasis and radiculopathy. An important gene associated with Myelitis is AQP4 (Aquaporin 4), and among its related pathways/superpathways are Innate Immune System and ERK Signaling. The drugs Mitoxantrone and Analgesics have been mentioned in the context of this disorder. Affiliated tissues include spinal cord, brain and bone marrow, and related phenotypes are no effect and no effect

Common Targets
NMDA receptor

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

Other Diseases

Netherton Syndrome | Menetrier Disease | Miyoshi Myopathy | Mitochondrial Myopathy | Lymphedema-distichiasis Syndrome | Prune Belly Syndrome | Neurodegeneration With Brain Iron Accumulation | Jaundice, Obstructive | Lissencephaly 2 | Adrenal Insufficiency | Pulmonary Alveolar Microlithiasis | Corneal Ulcer | Imerslund-Grasbeck Syndrome | Shwachman-Bodian-Diamond Syndrome | Seizures-scoliosis-macrocephaly Syndrome | Ocular Hypertension | Muscle Wasting | Acute Kidney Injury | Mucormycosis | Hyperparathyroidism-jaw Tumor Syndrome | Fetal And Neonatal Alloimmune Thrombocytopenia | Neurocutaneous Syndromes | Costello Syndrome | Occipital Neuralgia | Alpers Syndrome | Aarskog-Scott Syndrome | Localized Scleroderma | Infectious Diarrhea | Pilomatrix Carcinoma | Opisthorchiasis | Idiopathic Multicentric Castleman Disease | Thyrotoxic Periodic Paralysis | Diabetes Insipidus, Nephrogenic | Cryptorchidism | Blepharo-cheilo-odontic Syndrome | Acute Leukemia | Xeroderma Pigmentosum | Muscular Dystrophy | Porphyria | Atrial Septal Defect | Endometrial Hyperplasia | Frontometaphyseal Dysplasia | Meckel-Gruber Syndrome | Primary Pigmented Nodular Adrenocortical Disease | Lymphoma | Alzheimer Disease, Late Onset | Low Tension Glaucoma | Osteonecrosis Of The Jaw | Turner's Syndrome | Arthritis, Psoriatic | Polyneuropathy | Mucolipidosis Type IV | Pain | Craniosynostosis | Blastomycosis | Adenoma, Pleomorphic | Diffuse Palmoplantar Keratoderma | Rubeosis Iridis | Hereditary Spherocytosis | Macrophage Activation Syndrome | Parkinsonism | Basal Ganglia Cerebrovascular Disease | Intestinal Tuberculosis | Dowling-Degos Disease | Alveolar Capillary Dysplasia | Retinal Dystrophy, Early-onset Severe | Progressive Osseous Heteroplasia | Pyruvate Decarboxylase Deficiency | Facioscapulohumeral Muscular Dystrophy Type 1 | Cone Dystrophy | Chronic Leukemia | Schwannoma | Benign Familial Pemphigus | Encephalopathy | Nemaline Myopathy 8 | Leukoplakia | Ichthyosis Hystrix, Curth-Macklin Type | Autosomal Recessive Congenital Ichthyosis | Glomerulonephritis, Membranous | Choroideremia | Focal Facial Dermal Dysplasia | Leber Congenital Amaurosis | Shprintzen-Goldberg Syndrome | Postpoliomyelitis Syndrome | Subacute Sclerosing Panencephalitis | Blepharospasm | Amish Infantile Epilepsy Syndrome | Neurofibromatosis | Glioblastoma Multiforme | Fowler's Syndrome | Early Infantile Epileptic Encephalopathy | Pleomorphic Xanthoastrocytoma | Waardenburg Syndrome Type 4 | Tendinopathy | Renal Medullary Carcinoma | Aneurysm, Thoracic Aortic | Fanconi Syndrome | Spinocerebellar Ataxia Type 8 | Macular Corneal Dystrophy Type 1 | Oral Lichen Planus | Stuve-Wiedemann Syndrome | IMAGe Syndrome | Osteogenesis Imperfecta Type III | Narcolepsy | Chronic Lymphocytic Leukemia | Nephritis, Interstitial | Colorectal Adenoma | Retinal Diseases | Crisponi Syndrome | Dysgerminoma | Neutropenia | Microcephalic Osteodysplastic Primordial Dwarfism, Type I | Long QT Syndrome Type 1 | Intellectual Disability, Autosomal Dominant 5 | Nijmegen Breakage Syndrome | Esotropia | Sialoadenitis | Hypogammaglobulinemia | Hyperparathyroidism, Primary | Heroin Dependence | Hereditary Sensory Neuropathy Type 1 | Leri Pleonosteosis | Rhizomelic Chondrodysplasia Punctata | Osteochondrosis | Dysplastic Nevus | Hamartoma | Iron Metabolism Disorders | Sarcoma | Schistosomiasis Mansoni | Guttate Psoriasis | DNA Ligase IV Deficiency | Diffuse Intrinsic Pontine Glioma | Wilson's Disease | Galactosemia | Spitzoid Melanoma | Episodic Ataxia Type 2 | Multiple Hamartoma Syndrome | Papilloma | Sleep Disorder | Congenital Fiber-type Disproportion Myopathy | Congenital Stromal Corneal Dystrophy | Chromosome 8q21.11 Deletion Syndrome | Camptocormia | Treacher Collins Syndrome | Pure Red Cell Aplasia | Charcot-Marie-Tooth Disease, Type 1A | Inborn Errors Of Metabolism | Methemoglobinemia | Mitochondrial DNA Depletion Syndrome, Hepatocerebral Form | NDH Syndrome | Histiocytosis | Heart Failure | Kallmann Syndrome | Angiodysplasia | Cutaneous Mastocytosis | Pseudomyxoma Peritonei | Cushing Syndrome | Hyperbilirubinemia, Neonatal | Birk-Barel Syndrome | Urticaria | Thalassemia, Beta | Glucagonoma | Metachondromatosis | Spinocerebellar Ataxia Type 7 | Erythema Nodosum | Otitis Media | Endometriosis | Methylmalonic Acidemia | Myelitis, Transverse | Leiomyoma | Giant Cell Arteritis | Alagille Syndrome | Wagner Disease | Congenital Dyserythropoietic Anemia Type 1 | Congenital Heart Block | Neuroblastoma | Large Granular Lymphocytic Leukemia | Alpha-1 Antitrypsin Deficiency | Hartsfield Syndrome | Rubinstein-Taybi Syndrome | Wolcott-Rallison Syndrome | Chanarin-Dorfman Syndrome | Desbuquois Syndrome | Arthritis | Mesothelioma, Malignant | Pseudohypoparathyroidism Type 2 | Gangliosidosis, GM1 | Dementia, Vascular | Usher Syndrome | Mitochondrial DNA Depletion Syndrome, Encephalomyopathic Form | Cholestasis | Optic Neuritis | Hypogonadism | Beta-Propeller Protein-associated Neurodegeneration | Myocarditis | Hypotrichosis Simplex | Familial Hyperaldosteronism | Hemochromatosis Type 1 | Erythema Multiforme | Ocular Albinism Type 1 | Polyradiculopathy | Warsaw Breakage Syndrome | ADNP Syndrome | Autosomal Recessive Bestrophinopathy | Epidermolysis Bullosa | Pituitary Stalk Interruption Syndrome | Polycythemia Vera | Crohn's Disease | Aldosteronism | Infertility | Methemoglobinemia Type IV | Graves Disease | Facioscapulohumeral Muscular Dystrophy | Neurogenic Bladder | Crigler-Najjar Syndrome | Chronic Mucocutaneous Candidiasis | Sporadic Hemiplegic Migraine | Herpes Simplex Dermatitis | Multiple Myeloma | Congenital Muscular Dystrophy | Juvenile Hyaline Fibromatosis | Hypoglycemia | Hemangioblastoma | Myotonia | Sensory Ataxic Neuropathy, Dysarthria, And Ophthalmoparesis | Hyperphenylalaninemia | Leri-Weill Dyschondrosteosis | Peutz-Jeghers Syndrome | Osteoporosis-pseudoglioma Syndrome | HELLP Syndrome | Chondrodysplasia Punctata | Light Chain Amyloidosis | Nephrosclerosis | Behavioral Variant Of Frontotemporal Dementia | Congenital Tufting Enteropathy | Adenomatoid Tumor | Peripheral Neuropathy | Allan-Herndon-Dudley Syndrome | Retinal Coloboma | Hepatitis | Joubert Syndrome 2 | Inflammatory Myofibroblastic Tumor | Microphthalmia | Lymphoma, Primary Cutaneous Anaplastic Large Cell | Optic Nerve Hypoplasia, Bilateral | Hyperostosis | Hepatitis, Chronic | Dementia | Mosaic Variegated Aneuploidy Syndrome 2 | Unverricht-Lundborg Syndrome | Blood Protein Disorders | Charcot-Marie-Tooth Disease Type 4B1 | Headache | Twin-to-twin Transfusion Syndrome | Benign Recurrent Intrahepatic Cholestasis 1 | Kashin-Beck Disease | Porphyria, Variegate | Malignant Peripheral Nerve Sheath Tumor | Bone Marrow Necrosis | Cerebellofaciodental Syndrome | 3-hydroxyacyl-CoA Dehydrogenase Deficiency | Epidermolysis Bullosa Simplex, Localized | Primary Carnitine Deficiency | Bartsocas-Papas Syndrome | REM Sleep Behavior Disorder | Bronchiectasis | Angioimmunoblastic T-cell Lymphoma | Acute Anterior Uveitis | Gilbert Syndrome | Myoclonus | Asplenia | Anti-glomerular Basement Membrane Disease | Histiocytic Sarcoma | Congenital Nephrotic Syndrome | Autonomic Nervous System Disorders | Mountain Sickness | Central Pain Syndrome | Sorsby Fundus Dystrophy | Pyloric Stenosis, Infantile Hypertrophic | Nail-Patella Syndrome | Ebstein Anomaly | Megaloblastic Anemia | Presbyopia | Nephrotic Syndrome Type 1 | Dwarfism | Split Hand-foot Malformation | Chronic Thromboembolic Pulmonary Hypertension | Metachromatic Leukodystrophy | Charcot-Marie-Tooth Disease Type 2T | Cancer, Kidney | Cerebrotendinous Xanthomatosis | Gangliosidosis | Choroiditis | Pachyonychia Congenita | Multiple Sclerosis | Carotid Artery Disease | Pierre Robin Syndrome | Arrhythmogenic Right Ventricular Cardiomyopathy | Neurofibromatosis Type 2 | Melanoma, Uveal | Schizotypal Personality Disorder | Asthma | Meleda Disease | Neurodermatitis | Neurodevelopmental Disorder With Central Hypotonia And Dysmorphic Facies | Cerebral Amyloid Angiopathy | Mesial Temporal Lobe Epilepsy With Hippocampal Sclerosis | Glomerulonephritis, Membranoproliferative | Keloid | Prader-Willi Syndrome | Multiple Sclerosis, Primary Progressive | Mycosis Fungoides | Hyperglycemia | Charcot-Marie-Tooth Disease Axonal Type 2N | POEMS Syndrome | Dubin-Johnson Syndrome | Lattice Corneal Dystrophy Type 1 | Hepatitis D | Ameloblastoma | Irritable Bowel Syndrome | McLeod Syndrome | Desmosterolosis | Thromboembolism | Multiple Sclerosis, Secondary Progressive | Keratopathy | Erythrokeratodermia Variabilis | Harlequin Ichthyosis | Currarino Syndrome | Platyspondylic Lethal Skeletal Dysplasia, Torrance Type | Acne Vulgaris | Hyperlipidemia | Neuropathy | CHARGE Syndrome | Acute Lung Injury | Diabetic Encephalopathy | Pyruvate Kinase Deficiency | Hypopigmentation | Hypertension, Renal | Pulmonary Alveolar Proteinosis | Lymphoproliferative Disorders | Photosensitivity | Arterial Tortuosity Syndrome | Familial Partial Lipodystrophy | Myelodysplasia | Retinitis Pigmentosa 3 | Bethlem Myopathy | Bernard-Soulier Syndrome | Stuttering | Pneumonia, Viral | Best Macular Dystrophy | Woodhouse-Sakati Syndrome | Spinocerebellar Ataxia Type 27 | Seizures | Sponastrime Dysplasia | Hemorrhoids | Hypohidrotic Ectodermal Dysplasia | Papillon-Lefevre Syndrome | Blomstrand Osteochondrodysplasia | Binge Eating Disorder | Intestinal Hypomagnesemia 1 | Alopecia Totalis | Myofibrillar Myopathy | Ophthalmoplegia | Rickets | DEND Syndrome | Hypertriglyceridemia | Multisystemic Smooth Muscle Dysfunction Syndrome | Thrombophilia | Botulism | Myhre Syndrome | Crimean-Congo Hemorrhagic Fever | Peters-plus Syndrome | Farber Disease | Cellulitis | Spinocerebellar Ataxia Type 10 | Oligoastrocytoma | ICF Syndrome | Insulinoma | Craniometaphyseal Dysplasia | Galactosialidosis | Hereditary Mixed Polyposis Syndrome | Adenoma, Pituitary | Optic Nerve Diseases | Keratitis | Long QT Syndrome Type 3 | Anosmia, Congenital | Spinocerebellar Ataxia Type 21 | Mitochondrial Cytopathy | Malonyl-CoA Decarboxylase Deficiency | Astigmatism | Adams-Oliver Syndrome | Trichorhinophalangeal Syndrome | H Syndrome | Familial Glucocorticoid Deficiency | Cri-du-chat Syndrome | Trichuriasis | Cat Eye Syndrome | Gastritis, Atrophic | Hypertrophic Osteoarthropathy, Primary, Autosomal Recessive 2 | Thrombocytopenia