Alexander Disease
Alexander Disease
About the Disease
Alexander Disease, also known as alexander's disease, is related to leukodystrophy and multiple system atrophy 1, and has symptoms including muscle spasticity and seizures. An important gene associated with Alexander Disease is GFAP (Glial Fibrillary Acidic Protein), and among its related pathways/superpathways are Signaling by Receptor Tyrosine Kinases and Neuroscience. The drug Metronidazole has been mentioned in the context of this disorder. Affiliated tissues include brain, spinal cord and eye, and related phenotypes are macrocephaly and intellectual disability
Common Targets
GFAP | MALAT1 | HDAC6 | THRA | MALT1 | THRB
Note: If you'd like to get a target analysis report for Alexander Disease, 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 Alexander Disease at a cost 90% lower than traditional approaches, please feel free to contact us at BD@silexon.ai.
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Failure Syndrome 1 | Mountain Sickness | Sweet Syndrome | Pontocerebellar Hypoplasia | Acrodermatitis | Keratosis, Actinic | Polymyalgia Rheumatica | Paronychia | Lung Diseases | Bacterial Meningitis | Primrose Syndrome | Stevens-Johnson Syndrome | Cardiomyopathy, Hypertrophic | Glycogen Storage Disease Type 1 | Purpura, Thrombotic Thrombocytopenic | Apert Syndrome | Aplasia Cutis Congenita | Paget's Disease Of The Breast | Astigmatism | Anorectal Fistula | Congestive Heart Failure | Myofibromatosis | Motor Neuron Diseases | Porphyria, Acute Intermittent | Colitis, Lymphocytic | Insulin Resistance | Pulmonary Veno-occlusive Disease | Thyroid Dyshormonogenesis | Geleophysic Dysplasia | GAPO Syndrome | Niemann-Pick Disease, Type C | Keratopathy | Beta-Propeller Protein-associated Neurodegeneration | Diabetic Nephropathy | Cockayne Syndrome | Glycogen Storage Disease Type 4 | Genee-Wiedemann Syndrome | Spinocerebellar Ataxia Type 2 | Neuromuscular Disorders | Hypomyelination With Atrophy 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Intracranial Hypertension | Wilson's Disease | Omenn Syndrome | Polyradiculopathy | Hemophilia | Osteogenesis Imperfecta | Restrictive Dermopathy | Hemosiderosis | Stromal Corneal Dystrophy | Rubinstein-Taybi Syndrome | Personality Disorders | Eosinophilia | Hypophosphatemic Rickets With Hypercalciuria, Hereditary | Hereditary Elliptocytosis | Inflammatory Myopathy | Hennekam Lymphangiectasia-lymphedema Syndrome | Congenital Bile Acid Synthesis Defect | Spinocerebellar Ataxia Type 38 | Hypertension, Renal | TARP Syndrome | Xeroderma Pigmentosum Variant Type | Cystitis | Obesity | Thymoma, Malignant | Exfoliative Dermatitis | Chronic Kidney Disease | Adenosine Deaminase Deficiency | Hyperparathyroidism, Primary | Low Phospholipid Associated Cholelithiasis | Antiphospholipid Syndrome | Multiple System Atrophy | Protein S Deficiency | Poirier-Bienvenu Neurodevelopmental Syndrome | Krabbe Disease | Osteopetrosis | Lymphedema | Retinal Coloboma | Retinoblastoma | Glanzmann Thrombasthenia | Aldosteronism | Bardet-Biedl Syndrome | Juvenile Xanthogranuloma | Vestibular Disease | Epidermolytic Hyperkeratosis | Premature Ejaculation | Coronary Heart Disease | Polyomavirus Nephropathy | Cornelia De Lange Syndrome | Large Granular Lymphocytic Leukemia | Aarskog-Scott Syndrome | Mitochondrial DNA Depletion Syndrome, Encephalomyopathic Form | Dysgerminoma | Lymphoma, AIDS-related | Pheochromocytoma | Colitis, Collagenous | Basal Ganglia Cerebrovascular Disease | Frank-ter Haar Syndrome | Gyrate Atrophy Of The Choroid And Retina | Leigh Syndrome | Hyperinsulinemic Hypoglycemia | Hereditary Mixed Polyposis Syndrome | Hypobetalipoproteinemias | Proximal Symphalangism | Intermittent Claudication | Long QT Syndrome Type 2 | Alopecia Totalis | Autosomal Recessive Spastic Paraplegia Type 75 | Temporal Lobe Epilepsy | Corneal Ulcer | Metatropic Dysplasia | Fucosidosis | Gnathodiaphyseal Dysplasia | Tic Disorder | Pseudohypoparathyroidism Type 2 | Multifocal Motor Neuropathy | Reye 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