Disease

Cysticercosis

About the Disease
Cysticercosis, also known as neurocysticercosis, is related to echinococcosis and schistosomiasis. An important gene associated with Cysticercosis is IL6 (Interleukin 6), and among its related pathways/superpathways are Innate Immune System and MIF Mediated Glucocorticoid Regulation. The drugs Praziquantel and Benzocaine have been mentioned in the context of this disorder. Affiliated tissues include spinal cord, brain and skin, and related phenotypes are cerebral calcification and functional motor deficit

Common Targets
Carbonic Anhydrase (nonspecified subtype)

疾病靶点研报
Cysticercosis

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

Other Diseases

Chromosome 8q21.11 Deletion Syndrome | Epidermolysis Bullosa Simplex | Familial Exudative Vitreoretinopathy | Myelodysplasia | Pituitary Dwarfism | Early Infantile Epileptic Encephalopathy 4 | Myotonia | Guillain-Barre Syndrome | Werner's Syndrome | Bipolar Disorder | Mountain Sickness | Lymphoma, Follicular | DRESS Syndrome | Bicuspid Aortic Valve | Axenfeld-Rieger Syndrome | Kaposi Sarcoma | Parkinson Disease 6, Autosomal Recessive Early-onset | Intestinal Pseudo-obstruction | Hemophilia | Basal Ganglia Disease | Dysplastic Nevus | Fanconi Anemia | Congenital Poikiloderma | Coffin-Siris Syndrome | Pituitary Disorders | Choroideremia | Methylmalonic Acidemia | Tinea | Cancer, Lung | Amelanotic Melanoma | Orthostatic Intolerance | Leukocyte Adhesion Deficiency | Arteriovenous Malformations | Holt-Oram Syndrome | Aromatic L-amino Acid Decarboxylase Deficiency | Neurofibromatosis Type 1 | Autoimmune Polyendocrinopathy Syndrome Type I | Goiter, Nodular | Liebenberg Syndrome | Angioimmunoblastic T-cell Lymphoma | Central Retinal Artery Occlusion | Diabetic Macular Edema | CHARGE Syndrome | Progressive Familial Intrahepatic Cholestasis Type 3 | Gaucher Disease | Spinocerebellar Ataxia Type 14 | Lattice Corneal Dystrophy | Amblyopia | Ophthalmoplegia | Ichthyosis Hystrix, Curth-Macklin Type | Encephalocele | Ichthyosis | Pathological Gambling | Hidradenitis Suppurativa | Hemolytic Anemia | Hypercalciuria | Barrett Esophagus | Bartter Syndrome | Epicondylitis | Amyloidosis | 17-beta-hydroxysteroid Dehydrogenase X Deficiency | McKusick Type Metaphyseal Chondrodysplasia | Leigh Syndrome | Dupuytren Disease | Multiple Congenital Anomalies-hypotonia-seizures Syndrome 2 | Fatty Aldehyde Dehydrogenase Deficiency | Long QT Syndrome Type 2 | Takayasu's Arteritis | B-cell Prolymphocytic Leukemia | Hyperinsulinism-hyperammonemia Syndrome | Clouston Hidrotic Ectodermal Dysplasia | Light Chain Amyloidosis | Familial Digital Arthropathy-brachydactyly | Lymphoma | Measles | Osteoporosis, Postmenopausal | Epidermolysis Bullosa Simplex, Dowling-Meara Type | Acute Myeloid Leukemia | Ligneous Conjunctivitis | Leukocyte Adhesion Deficiency Type 1 | Stickler Syndrome | Lymphoma Lymphoblastic | Gyrate Atrophy Of The Choroid And Retina | Spinocerebellar Ataxia Type 2 | Familial Hemiplegic Migraine | Myocarditis | Persistent Truncus Arteriosus | Seminoma | Retinitis Pigmentosa 3 | Bursitis | Retinal Vasculitis | H Syndrome | Progressive Osseous Heteroplasia | Angioedema | Charcot-Marie-Tooth Disease, Type 1A | Muscle Wasting | Galactosemia | Small Lymphocytic Lymphoma | Proopiomelanocortin Deficiency | Usher Syndrome Type I | Cerebral Amyloid Angiopathy | Spondylometaphyseal Dysplasia | Fibromuscular Dysplasia | Acquired Partial Lipodystrophy | MIRAGE Syndrome | Scleroderma | Spondyloepimetaphyseal Dysplasia With Joint Laxity, Type 3 | Craniofrontonasal Syndrome | Adenomatoid Tumor | Antisocial Personality Disorder | Thin Basement Membrane Disease | Cerebellar Ataxia, Cayman Type | Dermatofibrosarcoma | Pouchitis | Leber Hereditary Optic Neuropathy | Wolfram Syndrome 2 | Obesity | Muckle-Wells Syndrome | Behcet's Disease | Cardiac Sarcoidosis | Odonto-onycho-dermal Dysplasia | Neurofibroma | Hyperferritinemia-cataract Syndrome | Intestinal Obstruction | Antisynthetase Syndrome | Schistosomiasis | Myotonic Disorders | Pendred Syndrome | Epidermolysis Bullosa | Colitis | Angiosarcoma Of The Breast | Erythromelalgia | 6-pyruvoyl-tetrahydropterin Synthase Deficiency | Charcot-Marie-Tooth Disease Type 2T | Achondrogenesis | Evans Syndrome | Mast Cell Leukemia | Warsaw Breakage Syndrome | Dermatitis | Scleritis | Huntington's Disease | Portal Vein Thrombosis | Polycystic Liver | Moyamoya Disease | Birk-Barel Syndrome | Eczema | Cocaine-Related Disorders | Schizophrenia, Paranoid | Neurofibromatosis Type 2 | Histiocytic Sarcoma | Hypoglycemia | Hypohidrotic Ectodermal Dysplasia, X-linked | Adenoma, Villous | Fukuyama Congenital Muscular Dystrophy | Craniopharyngioma | Blau Syndrome | Metabolic Diseases | Periodontitis | Exocrine Pancreatic Insufficiency | Inflammatory Bowel Disease | Oculodentodigital Dysplasia | Very Long-chain Acyl-CoA Dehydrogenase Deficiency | Hyperammonemia | Goldenhar Syndrome | Retinitis | Obesity, Morbid | Eclampsia | Perivascular Epithelioid Cell Tumor | Pleurisy | Plasma Cell Leukemia | HANAC Syndrome | GM2-gangliosidosis AB Variant | Cavitary Optic Disc Anomalies | Prostatitis | Primary Biliary Cholangitis | Hereditary Hemorrhagic Telangiectasia | Meier-Gorlin Syndrome | 3-methylcrotonyl-CoA Carboxylase Deficiency | Spinocerebellar Ataxia Type 28 | Immunoproliferative Disorders | Usher Syndrome Type II | Follicular Dendritic Cell Sarcoma | Scleroderma, Diffuse | Anorchia | Glycogen Storage Disease Type 3 | Silicosis | Glycogen Storage Disease Type 1b | Keloid | Conjunctivitis | Corneal Dystrophy | Intermittent Claudication | Vitamin B12 Deficiency | Venous Insufficiency | Leukoencephalopathy, Progressive Multifocal | Stomatitis | Hepatorenal Syndrome | Spondylo-ocular Syndrome | Peutz-Jeghers Syndrome | Temtamy Preaxial Brachydactyly Syndrome | Early Infantile Epileptic Encephalopathy 28 | Relapsing Polychondritis | Leri Pleonosteosis | Paracoccidioidomycosis | Hypopituitarism | Fetal And Neonatal Alloimmune Thrombocytopenia | Infantile Nephropathic Cystinosis | Infectious Diarrhea | Familial Retinal Arterial Macroaneurysm | Arthritis, Gouty | Mitochondrial Cytopathy | Cockayne Syndrome | Gastritis, Atrophic | Brachial Plexus Neuropathy | Frontometaphyseal Dysplasia | Pseudohypoaldosteronism | Localized Scleroderma | Blomstrand Osteochondrodysplasia | 3C Syndrome | Silver-Russell Syndrome | Bone Giant Cell Tumor | Myoclonus-dystonia Syndrome | Polyradiculopathy | Brugada Syndrome 1 | Heimler Syndrome | Eiken Syndrome | Alkaptonuria | Sleep Apnea, Obstructive | Chronic Lymphocytic Leukemia | Glomerulonephritis | Carbonic Anhydrase VA Deficiency | Holoprosencephaly | Chondromyxoid Fibroma | HIBCH Deficiency | Juvenile Myelomonocytic Leukemia | GNE Myopathy | Spondylocarpotarsal Synostosis Syndrome | Sleep Disorder | Ovarian Sex Cord-stromal Tumor | Common Cold | Von Willebrand Disease | Colitis, Microscopic | Brachydactyly | Endometritis | Membranous Nephropathy | Cutis Laxa | Epilepsy Of Infancy With Migrating Focal Seizures | ADNP Syndrome | Pulmonary Alveolar Proteinosis | Hemolytic Uremic Syndrome, Atypical | Porphyria Cutanea Tarda | Keratoconus | Compartment Syndrome | Benign Hereditary Chorea | Cystitis | Bronchitis, Chronic | Hyperphosphatasia With Intellectual Disability Syndrome 4 | Hypertrophic Osteoarthropathy, Primary, Autosomal Recessive 1 | Blepharoconjunctivitis | Camurati-Engelmann Disease | Neurodevelopmental Disorders | Angina Pectoris | Norrie Disease | Restless Legs Syndrome | Progressive External Ophthalmoplegia | Eosinophilic Asthma | Epilepsy | Bietti Crystalline Dystrophy | Mesothelioma, Malignant | Lentigo | Arthritis, Reactive | Retinal Dystrophy, Early-onset Severe | Hemochromatosis | Hypermethioninemia | Familial Hypertrophic Cardiomyopathy | Danon Disease | Fragile X Syndrome | Glycogen Storage Disease Type 1a | Micro Syndrome | Amyotrophic Lateral Sclerosis | Inflammatory Linear Verrucous Epidermal Nevus | Usher Syndrome Type III | Meningococcal Meningitis | DiGeorge Syndrome | Corticobasal Syndrome | Glutaric Aciduria Type 3 | Kabuki Syndrome | Lennox-Gastaut Syndrome | Wieacker-Wolff Syndrome | Spinocerebellar Ataxia Type 1 | Salla Disease | Infantile Spasm | Homocystinuria | Pelizaeus-Merzbacher Disease | Leukemia | Cholestasis, Intrahepatic | Glomerulonephritis, Membranoproliferative | Pain | Melanoma | Chronic Kidney Disease | Episodic Ataxia Type 2 | Angioedema, Hereditary | Cutaneous T-cell Lymphoma | Esophagitis, Eosinophilic | Schizencephaly | Sialidosis | Chediak-Higashi Syndrome | Vascular Cognitive Impairment | Infantile Refsum Disease | Primary Carnitine Deficiency | Sotos Syndrome | Swine Influenza | Muscular Dystrophy | Beta-Propeller Protein-associated Neurodegeneration | Congenital Disorders Of Glycosylation | Medium-chain Acyl-CoA Dehydrogenase Deficiency | Hyperlipidemia | Rhinitis | Achromatopsia | Hypomyelination With Atrophy Of Basal Ganglia And Cerebellum | Ornithine Transcarbamylase Deficiency | Brooke-Spiegler Syndrome | Cousin Syndrome | Epidermolysis Bullosa Dystrophica | Christianson Syndrome | Hepatic Veno-occlusive Disease | Adrenoleukodystrophy, X-linked | Conjunctivitis, Allergic | Barakat Syndrome | Protein S Deficiency | Dengue Hemorrhagic Fever | Nephropathy | Impulse Control Disorder | Bone Marrow Necrosis | Spondylocostal Dysostosis | Thymoma, Malignant | Gerodermia Osteodysplastica | Arrhythmogenic Right Ventricular Cardiomyopathy | Senior-Loken Syndrome | Dyslipidemia | Wolcott-Rallison Syndrome | Sturge-Weber Syndrome | LRBA Deficiency | Spinocerebellar Ataxia Type 17 | Keratoacanthoma | Long QT Syndrome Type 1 | Atopy | Nager Acrofacial Dysostosis | Photosensitivity | Optic Nerve Diseases | Juvenile Hyaline Fibromatosis | Congenital Bile Acid Synthesis Defect | Iron Deficiency Anemia | Schistosomiasis Mansoni | Autonomic Neuropathy | Filariasis | Neurodegeneration With Brain Iron Accumulation | Blood Protein Disorders | Riboflavin Transporter Deficiency Neuronopathy | Spitz Nevus | Trichotillomania | Anorectal Malformations | Larsen Syndrome | Ebstein Anomaly | Hepatitis, Chronic | Lassa Fever | Retinal Degeneration | X-linked Sideroblastic Anemia | Nephrotic Syndrome | AIDS | Neuroma | Microcephalic Osteodysplastic Primordial Dwarfism, Type II | Focal Facial Dermal Dysplasia | Neurodermatitis | Recurrent Respiratory Papillomatosis | Renal Hypomagnesemia 3 | Cole-Carpenter Syndrome | ACTH-independent Macronodular Adrenal Hyperplasia | Mitochondrial Disease | Atopic Dermatitis | Inflammatory Myopathy | Kohlschutter-Tonz Syndrome | Encephalopathy, Ethylmalonic | Idiopathic Pulmonary Fibrosis | Muir-Torre Syndrome | Periventricular Leukomalacia | Familial Dysautonomia | Liver Failure | Guttate Psoriasis | Addison Disease | Hyperthyroidism | Pantothenate Kinase-associated Neurodegeneration | Thrombosis | Pancreatitis, Chronic | Congenital Ichthyosiform Erythroderma | Osmotic Demyelination Syndrome | Pneumoconiosis | Familial Mediterranean Fever | Primary Hyperoxaluria Type 1 | Usher Syndrome | Reflex Epilepsy