Multiple Sclerosis, Secondary Progressive
Multiple Sclerosis, Secondary Progressive
About the Disease
Secondary Progressive Multiple Sclerosis, also known as multiple sclerosis, secondary progressive, is related to relapsing-remitting multiple sclerosis and multiple sclerosis. An important gene associated with Secondary Progressive Multiple Sclerosis is MBP (Myelin Basic Protein), and among its related pathways/superpathways are superpathway of L-citrulline metabolism and Amino acid metabolism. The drugs Dalfampridine and Cladribine have been mentioned in the context of this disorder. Affiliated tissues include bone marrow, brain and spinal cord, and related phenotypes are immune system and hematopoietic system
Common Targets
Carnitine O-Palmitoyltransferase 1 (CPT-1) (nonspecified subtype) | NF-kappaB (NFkB) | CYP1A1 | TRPC5 | PDE10A | Tyrosine Kinase (nonspecified subtype) | CD40 | Glutamate Transporter (nonspecified subtype) | IL7R | KIT | MTNR1B | MS4A1 | IFNG | MIR21 | ADA | G7099 | Adenosine deaminase (nonspecified subtype) | LINGO1 | ARNT | NPY | G196 | Interferon alpha/beta Receptor (nonspecified subtype) | G5133 | CYP1A2 | HLA-DQB1 | LYN | EBP | TPH2 | MIF | VMP1 | S1PR5 | LILRA3 | IL13 | LRRN1 | HLA-DRB1 | KRR1 | DPP6 | NQO1 | S1PR1 | RIPK1 | BTK | CCL20 | CYP1B1 | IL1RN | Phosphodiesterase IV (PDE4) (nonspecified subtype) | G3569 | FGFR3 | Tubulin | RGMA | Interleukin 17 (nonspecified subtype) | ESR2 | VDR | AHRR | Sodium channel (nonspecified subtype) | Voltage-Gated Sodium Channel Complex | CYSLTR1 | Integrin alpha4beta1 (VLA-4) receptor

Note: If you'd like to get a target analysis report for Multiple Sclerosis, Secondary Progressive, 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 Multiple Sclerosis, Secondary Progressive at a cost 90% lower than traditional approaches, please feel free to contact us at BD@silexon.tech.
Other Diseases
Adrenoleukodystrophy, X-linked | Pathological Gambling | Congenital Hereditary Endothelial Dystrophy Type I | Spinocerebellar Ataxia | Chromosome 17q21.31 Deletion Syndrome | Cenani-Lenz Syndactyly Syndrome | Ectopia Lentis, Isolated, Autosomal Recessive | Placenta Previa | Fanconi Anemia | Myositis | Tangier Disease | Congenital Mirror Movements | Urethritis | Lattice Corneal Dystrophy | Spondylolisthesis | Dysplastic Nevus | Dystonia | Anovulation | Chitayat Syndrome | Arrhythmogenic Right Ventricular Cardiomyopathy | Hemochromatosis Type 1 | Ovarian Sex Cord-stromal Tumor | Majeed Syndrome | Pseudohypoparathyroidism Type 1A | Rheumatic Heart Disease | Aldosterone Synthase Deficiency | Mitochondrial Cytopathy | Glycogen Storage Disease Type 9 | Hereditary Coproporphyria | Spinal Cord Diseases | Familial Hyperaldosteronism | Cockayne Syndrome | Fetal Alcohol Syndrome | Olmsted Syndrome | Rhinitis | Tonsillitis | Leukemia | Microphthalmia, Syndromic 7 | Sporadic Hemiplegic Migraine | Dominant Optic Atrophy | Charcot-Marie-Tooth Disease Type 2T | Oculocutaneous Albinism Type 2 | Stromal Corneal Dystrophy | Transient Bullous Dermolysis Of The Newborn | Hypertension, Portal | Lymphoma, Mantle Cell | Leber Hereditary Optic Neuropathy | Melnick-Needles Syndrome | Eosinophilic Asthma | Cantu Syndrome | Wilson's Disease | Corneal Ulcer | Congenital Primary Aphakia | D-2-Hydroxyglutaric Aciduria | Pseudohypoparathyroidism Type 1C | Persistent Mullerian Duct Syndrome | Cutaneous T-cell Lymphoma | Arthropathy | Lyme Disease | Genitopatellar Syndrome | Diabetic Encephalopathy | Arteriosclerosis | Thrombophilia | Autoimmune Disease | Brachydactyly | Depression | Hidradenitis | Benign Familial Pemphigus | Agammaglobulinemia | Constipation | Hyperparathyroidism, Primary | Hepatopulmonary Syndrome | Charcot-Marie-Tooth Disease, Type 2A | Stickler Syndrome | Cholangitis | Hemangioma | Pain | Diabetic Macular Edema | WAGR Syndrome | Gigantism | Erdheim-Chester Disease | Epidermolysis Bullosa Acquisita | Dwarfism | Spinocerebellar Ataxia Type 2 | Familial Cerebral Amyloid Angiopathy | Alpha-1 Antitrypsin Deficiency | Hemosiderosis | Spinocerebellar Ataxia Type 5 | Hartsfield Syndrome | Fundus Albipunctatus | Juvenile Myoclonic Epilepsy | Sarcoidosis | Alopecia Areata | Primary Lateral Sclerosis | Glycogen Storage Disease Type 0 | Anemia | Keratoacanthoma | Chylomicron Retention Disease | Atelosteogenesis Type 2 | Hypersensitivity | Acrodermatitis Enteropathica | Erectile Dysfunction | Nephrosclerosis | Carbonic Anhydrase VA Deficiency | Ollier Disease | Bietti Crystalline Dystrophy | Hypopituitarism | Ganglioneuroma | Pseudohypoaldosteronism | Allergic Contact Dermatitis | Subacute Sclerosing Panencephalitis | Anorectal Malformations | Charcot-Marie-Tooth Disease Axonal Type 2N | Creatine Deficiency Syndrome Due To AGAT Deficiency | Hereditary Sensory And Autonomic Neuropathy | Situs Inversus | Ovarian Hyperstimulation Syndrome | Thyroiditis, Autoimmune | Gallstones | Acute Coronary Syndrome | Contact Dermatitis | Polycythemia | Woodhouse-Sakati Syndrome | Kidney Stones | Polycystic Kidney, Autosomal Dominant | Carney-Stratakis Syndrome | Nance-Horan Syndrome | Hereditary Sensory Neuropathy Type 1 | Fontaine Progeroid Syndrome | Blue Nevus | Adenoma, Pleomorphic | Gastrointestinal Disorders | Neurocutaneous Syndromes | Diabetes Mellitus, Transient Neonatal | Polymicrogyria | Congenital Heart Block | Cavitary Optic Disc Anomalies | Hereditary Inclusion Body Myopathy | Lennox-Gastaut Syndrome | Neurofibromatosis Type 1 | Bronchitis, Chronic | Stuttering | Hereditary Xerocytosis | Achondrogenesis | Purpura | Hypoparathyroidism | Spinocerebellar Ataxia Type 40 | Hypermethioninemia | Dysmorphophobia | Cataplexy | Myoclonus | Crouzon Syndrome With Acanthosis Nigricans | Acral Lentiginous Melanoma | Kohlschutter-Tonz Syndrome | Dubin-Johnson Syndrome | Congenital Tufting Enteropathy | Portal Vein Thrombosis | Liver Diseases | Seminoma | Sotos Syndrome | Sarcoma, Alveolar Soft Part | Scleroderma, Diffuse | Osteopetrosis | Kindler Syndrome | Lesch-Nyhan Syndrome | Molybdenum Cofactor Deficiency | Non-bullous Congenital Ichthyosiform Erythroderma | Pneumonia, Viral | Premenstrual Syndrome | Megacystis-microcolon-intestinal Hypoperistalsis Syndrome | Lymphangioma | Phenylketonuria II | Neuroblastoma | Cannabis Abuse | Japanese Encephalitis | Hyperphosphatasia With Intellectual Disability Syndrome 4 | Renal Tubular Dysgenesis | Ureteropelvic Junction Obstruction | Long QT Syndrome Type 1 | Waardenburg Syndrome | Ichthyosis Bullosa Of Siemens | Goiter, Nodular | Gray Platelet Syndrome | Spinocerebellar Ataxia Type 16 | Chromosome 5q Deletion Syndrome | Autoimmune Interstitial Lung, Joint, And Kidney Disease | Meckel-Gruber Syndrome | Anti-NMDA Receptor Encephalitis | Homocystinuria | Hereditary Spastic Paraplegia | Cyclic Vomiting Syndrome | Multiple Congenital Anomalies-hypotonia-seizures Syndrome 2 | Neutropenia | B-cell Chronic Lymphocytic Leukemia | Primary Progressive Nonfluent Aphasia | Spina Bifida | Schwannoma | Systemic Lupus Erythematosus | Dermatomyositis | Osteogenesis Imperfecta Type III | Myelitis | Mitochondrial DNA Depletion Syndrome, Myopathic Form | Congenital Hemolytic Anemia | Pernicious Anemia | Muscular Dystrophy | Coffin-Lowry Syndrome | Spondyloperipheral Dysplasia | Basal Ganglia Disease | Hypohidrotic Ectodermal Dysplasia, X-linked | Periventricular Leukomalacia | Bladder Exstrophy | Osteogenesis Imperfecta | Oculocutaneous Albinism Type 4 | Dysthymia | Autoimmune Hemolytic Anemia | Sclerocornea | Farber Disease | Charcot-Marie-Tooth Disease Type 3 | Congenital Absence Of Vas Deferens | Glycogen Storage Disease Type 3 | Enlarged Vestibular Aqueduct | Glioma | Cardiomyopathy, Dilated, 1L | Fragile X Syndrome | Neovascular Glaucoma | Crigler-Najjar Syndrome | Amblyopia | Tenosynovial Giant Cell Tumor | Acrodermatitis | Marshall-Smith Syndrome | Keratosis | Alpers Syndrome | Marinesco-Sjogren Syndrome | Hermansky-Pudlak Syndrome | Pseudoachondroplasia | Peters-plus Syndrome | Hypoalbuminemia | Wolff-Parkinson-White Syndrome | Hereditary Neuropathy With Liability To Pressure Palsies | Thyroid Dyshormonogenesis | Spondyloarthritis | Relapsing Polychondritis | Basal Ganglia Cerebrovascular Disease | Tetraplegia | Desmosterolosis | Craniosynostosis | Language Disorders | Splenomegaly | Metaphyseal Chondrodysplasia, Schmid Type | Syphilis | Craniopharyngioma | Panuveitis | Cardiofaciocutaneous Syndrome | Thrombotic Microangiopathy | Gastritis, Atrophic | Autosomal Recessive Spastic Paraplegia Type 35 | Hypotonia-cystinuria Syndrome | ACTH-independent Macronodular Adrenal Hyperplasia | Episodic Ataxia Type 1 | Abetalipoproteinemia | Neuroleptic Malignant Syndrome | Myositis, Focal | McCune-Albright Syndrome | Congenital Dyserythropoietic Anemia | Peeling Skin Syndrome Type B | Aarskog-Scott Syndrome | Hypotrichosis | Charcot-Marie-Tooth Disease Type 4B1 | Pyelonephritis | Megaloblastic Anemia | Episodic Ataxia Type 2 | Crohn's Disease | Dent Disease | Aldosterone Deficiency | Congenital Stromal Corneal Dystrophy | Coloboma | Usher Syndrome Type III | Viral Meningitis | Diffuse Intrinsic Pontine Glioma | Colitis | Multisystemic Smooth Muscle Dysfunction Syndrome | Holt-Oram Syndrome | Hypertension | Vitamin B12 Deficiency | Tay-Sachs Disease | Anal Fissure | Osteosarcoma | Rhabdomyosarcoma, Embryonal | Holoprosencephaly | Craniofacial Dysostosis | Pigment Dispersion Syndrome | Medium-chain Acyl-CoA Dehydrogenase Deficiency | Birt-Hogg-Dube Syndrome | Low Tension Glaucoma | Avellino Corneal Dystrophy | Lymphoproliferative Disease, X-linked | Tyrosinemia | Albinism | Leishmaniasis, Cutaneous | Pseudo-pseudohypoparathyroidism | Histiocytic Sarcoma | Familial Pheochromocytoma-paraganglioma | Nicolaides-Baraitser Syndrome | Mitochondrial DNA Depletion Syndrome | Cousin Syndrome | McKusick Type Metaphyseal Chondrodysplasia | Hyperlipidemia | Angiosarcoma Of The Breast | Hypotrichosis Simplex | Fatty Aldehyde Dehydrogenase Deficiency | Rubinstein-Taybi Syndrome | Ehlers-Danlos Syndrome | Hereditary Elliptocytosis | Otopalatodigital Syndrome Type 2 | Light Chain Amyloidosis | Canavan Disease | Kawasaki Disease | Acute Kidney Injury | Bare Lymphocyte Syndrome | Pyruvate Decarboxylase Deficiency | Measles | Binge Eating Disorder | Bulimia Nervosa | Osteosclerosis | Hemangioblastoma | Central Retinal Artery Occlusion | Lung Diseases | Scoliosis | Leber Congenital Amaurosis | Danon Disease | Waardenburg Syndrome Type 2 | Microvillus Inclusion Disease | Disseminated Superficial Actinic Porokeratosis | Acute Generalized Exanthematous Pustulosis | Acute Motor Axonal Neuropathy | Glanzmann Thrombasthenia | Cervicitis | Dental Caries | Ulcerative Colitis | Pierpont Syndrome | Pheochromocytoma | Nemaline Myopathy 8 | Macrophagic Myofasciitis | Autosomal Recessive Congenital Ichthyosis | Takenouchi-Kosaki Syndrome | Seasonal Mood Disorder | Basal Ganglia Disease, Biotin-responsive | Atopy | Liver Failure | Carcinoma In Situ | Encephalopathy, Ethylmalonic | Urofacial Syndrome | Optic Neuropathy | Malnutrition | Encephalocele | Lymphangioleiomyomatosis | Autoimmune Polyendocrine Syndrome | Biotinidase Deficiency | Filariasis | Carey-Fineman-Ziter Syndrome | Castleman Disease | Psoriasis | Spinocerebellar Ataxia Type 6 | Learning Disability | Epidermolysis Bullosa | Jawad Syndrome | Asthma | Spinocerebellar Ataxia Type 12 | Stroke, Ischemic | Enhanced S-cone Syndrome | Gerodermia Osteodysplastica | Hereditary Hemorrhagic Telangiectasia | Unverricht-Lundborg Syndrome | Choreoathetosis, Hypothyroidism, And Neonatal Respiratory Distress | Bipolar Disorder | Becker Muscular Dystrophy | Pterygium | Sarcoma, Endometrial Stromal | Antithrombin III Deficiency | Pseudohermaphroditism | Cutis Laxa | Shock, Cardiogenic | Saethre-Chotzen Syndrome | Charcot-Marie-Tooth Disease Type 4D | Spondylo-megaepiphyseal-metaphyseal Dysplasia | Glutaric Aciduria Type 3 | Mucolipidosis Type III | Microcephaly | Pituitary Stalk Interruption Syndrome | Metatropic Dysplasia | Pure Autonomic Failure | Alzheimer Disease, Late Onset | Pupil Disorders | Arthritis, Gouty | Mitochondrial Myopathy | Aplasia Cutis Congenita | Spitzoid Melanoma | Colon Adenoma | Kabuki Syndrome 2 | Familial Glucocorticoid Deficiency