Subacute Sclerosing Panencephalitis

About the Disease
Subacute Sclerosing Panencephalitis, also known as sspe, is related to measles and papilledema. An important gene associated with Subacute Sclerosing Panencephalitis is CD46 (CD46 Molecule), and among its related pathways/superpathways are Innate Immune System and MIF Mediated Glucocorticoid Regulation. Affiliated tissues include brain, cortex and heart, and related phenotypes are infectious encephalitis and no effect

Common Targets
LGMN | IFNG | G5133 | IL12B | TLR3

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

Other Diseases

Gigantism | Hyperphosphatasia With Intellectual Disability Syndrome 4 | Ischemia | Sclerocornea | Schnyder Crystalline Corneal Dystrophy | Hypohidrotic Ectodermal Dysplasia, X-linked | Triple A Syndrome | Cystitis, Interstitial | Seizures-scoliosis-macrocephaly Syndrome | Acrodermatitis | B-cell Chronic Lymphocytic Leukemia | Pernicious Anemia | Aceruloplasminemia | Blomstrand Osteochondrodysplasia | Fontaine Progeroid Syndrome | Megaloblastic Anemia | Antisocial Personality Disorder | Hypertrophic Osteoarthropathy, Primary, Autosomal Recessive 1 | Ichthyosis | Carbohydrate Metabolism Disorders | Spinocerebellar Ataxia Type 20 | Chondromyxoid Fibroma | Focal Facial Dermal Dysplasia | Mixed Connective Tissue Disease | Idiopathic Pulmonary Fibrosis | Spinocerebellar Ataxia Type 6 | Optic Neuritis | Micropenis | Cerebrovascular Disorders | Binge Eating Disorder | Periventricular Nodular Heterotopia | Retinal Diseases | Hyperthyroidism | Endometriosis | Polymyalgia Rheumatica | Citrullinemia | Basal Cell Nevus Syndrome | Cystinuria | Hepatitis C, Chronic | Antisynthetase Syndrome | Alazami Syndrome | Early Infantile Epileptic Encephalopathy 13 | Hypodontia | Hereditary Xerocytosis | Narcolepsy | Torticollis | Lesch-Nyhan Syndrome | Behcet's Disease | Mountain Sickness | Nevus | Neuroma | Spinocerebellar Ataxia Type 14 | Vasculitis | Amish Infantile Epilepsy Syndrome | Tinea Versicolor | Juvenile Myelomonocytic Leukemia | Niemann-Pick Disease, Type B | Diabetes Insipidus | Overactive Bladder | Thrombocytopenia | Mannosidase Deficiency Diseases | Fuchs Heterochromic Iridocyclitis | Hyperlipidemia | Still Disease | Spondylometaphyseal Dysplasia | Anorexia Nervosa | Lymphoma, AIDS-related | Dyslipidemia | Hypertension, Renal | Cancer, Brain | Ventricular Septal Defect | Esophageal Motility Disorders | Urolithiasis | Spinal Muscular Atrophy | Cardiac Arrest | Acne | Pycnodysostosis | Hypertension, Renovascular | Peripheral T-cell Lymphoma | Neuromyotonia | Hemorrhagic Disorders | 6-pyruvoyl-tetrahydropterin Synthase Deficiency | Niemann-Pick Disease, Type A | Astrocytoma, Anaplastic | Tinea | Apparent Mineralocorticoid Excess Syndrome | Myopia | Esotropia | Treacher Collins Syndrome | Rhinitis | Spondyloarthritis | Olmsted Syndrome | Birt-Hogg-Dube Syndrome | Parapsoriasis | Colon Adenoma | Dowling-Degos Disease | Fetal Akinesia Deformation Sequence | Placenta Previa | Heart Septal Defects | Fetal And Neonatal Alloimmune Thrombocytopenia | Lichen Planus | Ophthalmia, Sympathetic | Wiedemann-Steiner Syndrome | Takotsubo Cardiomyopathy | Fukuyama Congenital Muscular Dystrophy | Hypermetropia | Schizophrenia, Paranoid | Bardet-Biedl Syndrome | Cerebrotendinous Xanthomatosis | Pseudoexfoliation Syndrome | PASLI Disease | Maple Syrup Urine Disease | Sickle Cell Anemia | Onchocerciasis | Mastitis | Wolman Disease | Pitt-Hopkins Syndrome | Glomerulonephritis, Membranoproliferative | Tularemia | Niemann-Pick Disease | Charcot-Marie-Tooth Disease, Type 1A | Down Syndrome | Fragile X Syndrome | Acute Tubular Necrosis | Pontocerebellar Hypoplasia | Headache | Costello Syndrome | Porphyria Cutanea Tarda | Intestinal Hypomagnesemia 1 | Osteomyelitis | Loeys-Dietz Syndrome Type 4 | Budd-Chiari Syndrome | Combined Deficiency Of Factor V And Factor VIII | Triphalangeal Thumb-polysyndactyly Syndrome | Palsy, Cerebral | Diabetes Insipidus, Neurogenic | Malonyl-CoA Decarboxylase Deficiency | Platyspondylic Lethal Skeletal Dysplasia, Torrance Type | Inflammatory Myofibroblastic Tumor | Tyrosine Hydroxylase Deficiency | Cancer, Lung | Keratoacanthoma | Osteopetrosis | Mabry Syndrome | Bainbridge-Ropers Syndrome | Mucolipidosis Type III | Arthritis, Reactive | Fanconi Syndrome | Congenital Muscular Dystrophy | Osteoglophonic Dysplasia | Primary Torsion Dystonia | LMNA-related Congenital Muscular Dystrophy | Fahr Disease | Aldosteronism | Lipid Storage Myopathy | Combined Pituitary Hormone Deficiency | Familial Digital Arthropathy-brachydactyly | Cardiofaciocutaneous Syndrome | Familial Exudative Vitreoretinopathy | Kernicterus | Pachyonychia Congenita | Charcot-Marie-Tooth Disease Type 2T | Phosphoenolpyruvate Carboxykinase Deficiency, Cytosolic | Coloboma | Facioscapulohumeral Muscular Dystrophy | Brenner Tumor | Pyelonephritis | Polycystic Liver | Epidermolysis Bullosa | Craniosynostosis | Polycystic Kidney, Autosomal Dominant | CREST Syndrome | Choriocarcinoma | Cancer, Kidney | Multiple Sclerosis, Chronic Progressive | Hyperlipidemia, Familial Combined | Sclerosteosis 2 | Spermatocele | WAGR Syndrome | Beare-Stevenson Syndrome | Poretti-Boltshauser Syndrome | Blau Syndrome | Steel Syndrome | Epidermolytic Ichthyosis, Annular | Encephalopathy, Glycine | Chanarin-Dorfman Syndrome | Axenfeld-Rieger Syndrome | Oculopharyngeal Muscular Dystrophy | Hepatitis, Autoimmune | Macrophagic Myofasciitis | Proteasome-associated Autoinflammatory Syndrome 2 | Keratopathy | Pontocerebellar Hypoplasia Type 7 | Pilomatrix Carcinoma | Amelogenesis Imperfecta | Alpers Syndrome | Autoimmune Disease | Miyoshi Myopathy | Glucagonoma | Teratozoospermia | Metaphyseal Chondrodysplasia, Schmid Type | Hypertension, Portal | Tumoral Calcinosis | Silicosis | Roberts Syndrome | Ependymoma | Schizoaffective Disorder | Renal Tubular Acidosis | Anorectal Fistula | Hypothyroidism | Keratoconjunctivitis | Plasmacytoma | Keratosis | Lafora Disease | Presbycusis | Sarcoma, Endometrial Stromal | LRBA Deficiency | Adenoma, Pituitary | Hyperprolactinemia | Crimean-Congo Hemorrhagic Fever | Sleep Apnea, Central | Incontinentia Pigmenti | Kaposiform Hemangioendothelioma | Paternal Uniparental Disomy Of Chromosome 14 | Graves Disease | Purpura | Knobloch Syndrome | Myasthenia Gravis | Hidradenitis Suppurativa | Histoplasmosis | Erythema Nodosum | Aneurysm, Thoracic Aortic | Batten Disease | Delirium | Histiocytic Sarcoma | Pulmonary Alveolar Proteinosis | Congenital Ichthyosiform Erythroderma | Leukemia-lymphoma, Adult T-cell | Riboflavin Transporter Deficiency Neuronopathy | Liver Failure | Melanocytic Nevus | Methemoglobinemia Type IV | Marfan Syndrome | Gallstones | Persistent Mullerian Duct Syndrome | Pseudohypoaldosteronism | Glycogen Storage Disease Type 1b | Congenital Bile Acid Synthesis Defect | Netherton Syndrome | Gaucher Disease | Basan Syndrome | Sarcoidosis, Pulmonary | 3-methylcrotonyl-CoA Carboxylase Deficiency | Heroin Dependence | Epilepsy Of Infancy With Migrating Focal Seizures | Inflammatory Bowel Disease | Familial Pheochromocytoma-paraganglioma | Cellulitis | Cardiomyopathy, Peripartum | Lymphoma Lymphoblastic | Familial Episodic Pain Syndrome | Corneal Dystrophy And Perceptive Deafness | Esophageal Adenocarcinoma | Congenital Dyserythropoietic Anemia Type 1 | Corneal Ulcer | Chronic Enteropathy Associated With SLCO2A1 Gene | Oculocutaneous Albinism Type 4 | Hereditary Multiple Exostoses | Neurofibromatosis | Lipodystrophy | Pneumonia, Viral | Leber Congenital Amaurosis | Bronchitis | Non-proliferative Diabetic Retinopathy | Methylmalonic Aciduria And Homocystinuria, CblC Type | Perry Syndrome | Glutathione Synthetase Deficiency | Hypophosphatemic Rickets, Autosomal Recessive, 1 | Fibromuscular Dysplasia | Rubinstein-Taybi Syndrome | Encephalopathy, Hepatic | Infertility, Male | Sleep Apnea, Obstructive | Glaucomatocyclitic Crisis | Superficial Spreading Melanoma | Motor Neuron Diseases | Juvenile Hyaline Fibromatosis | Pseudohypoparathyroidism Type 1C | Retinal Vasculitis | VEXAS Syndrome | Congenital Aniridia | Arteriosclerosis | Progressive Familial Intrahepatic Cholestasis Type 1 | Partington Syndrome | Stuttering | Graft-versus-host Disease | Nasodigitoacoustic Syndrome | CDKL5 Deficiency Disorder | Non-epidermolytic Palmoplantar Keratoderma | GAPO Syndrome | Lymphedema | Tyrosinemia | Zollinger-Ellison Syndrome | Angioedema | X-linked Acrogigantism | Leukoplakia | Microcephaly | Schamberg Disease | Glomerulonephritis, Membranous | Glycogen Storage Disease Type 9 | Charcot-Marie-Tooth Disease Type 4D | Blepharo-cheilo-odontic Syndrome | Frontotemporal Dementia | Primary Hyperoxaluria | Hyperuricemic Nephropathy, Familial Juvenile | Hydrocephalus | Metabolic Diseases | Fucosidosis | Thanatophoric Dysplasia | Tardive Dyskinesia | Hyperinsulinemia | Osteomalacia | Chromosome 8q21.11 Deletion Syndrome | Hypotrichosis | Paraganglioma | Huntington's Disease-like 2 | Osteitis | 17-beta-hydroxysteroid Dehydrogenase X Deficiency | Loeys-Dietz Syndrome | Parkinson Disease 6, Autosomal Recessive Early-onset | Contact Dermatitis | Kindler Syndrome | Angina Pectoris | Wolfram Syndrome | Warsaw Breakage Syndrome | Kidney Stones | Cryopyrin-associated Periodic Syndromes | Lateral Meningocele Syndrome | Retinopathy, Diabetic | Cavitary Optic Disc Anomalies | Pfeiffer Syndrome | Metanephric Adenoma | Mitochondrial DNA Depletion Syndrome, Myopathic Form | Psoriasis | Polycystic Kidney, Autosomal Recessive | Depression | 3-methylglutaconic Aciduria | Ureteropelvic Junction Obstruction | LEOPARD Syndrome | Alpha-1 Antitrypsin Deficiency | Spinocerebellar Ataxia Type 1 | Thrombotic Microangiopathy | Pouchitis | Pelvic Inflammatory Disease | Bartsocas-Papas Syndrome | Oculocutaneous Albinism Type 1 | Charcot-Marie-Tooth Disease, Type 2 | Spinocerebellar Ataxia Type 21 | Spondylocarpotarsal Synostosis Syndrome | Dermatomyositis | Sturge-Weber Syndrome | Chromosome 9q34.3 Deletion Syndrome | Hypopigmentation | Pyruvate Kinase Deficiency | Meningitis | Pemphigus | Small Lymphocytic Lymphoma | Rheumatoid Arthritis | Disseminated Intravascular Coagulation | Central Pain Syndrome | Trismus-pseudocamptodactyly Syndrome | Pancreatitis, Chronic | MELAS Syndrome | Impetigo | Thrombocythemia, Essential | Myoclonic Epilepsy With Ragged Red Fibers | Hypoplastic Left Heart Syndrome | Thymoma, Malignant | Parkinsonism | Sulfite Oxidase Deficiency | Atelosteogenesis Type 1 | Hypertension | Hidradenitis | Rett Syndrome | Keratitis | Methemoglobinemia | Supravalvular Aortic Stenosis | Tetanus | Mood Disorder | Autosomal Recessive Spastic Paraplegia Type 75 | Stroke | Kabuki Syndrome | Beta-Propeller Protein-associated Neurodegeneration | Autosomal Recessive Spastic Paraplegia Type 54 | Blepharitis | Thyroid Hormone Resistance | Prolidase Deficiency | Peeling Skin Syndrome Type B | Charcot-Marie-Tooth Disease Type 2D | TARP Syndrome