Disease

Hodgkin Lymphoma

About the Disease
Lymphoma, Hodgkin, Classic, also known as hodgkin lymphoma, is related to mantle cell lymphoma and primary cutaneous t-cell non-hodgkin lymphoma. An important gene associated with Lymphoma, Hodgkin, Classic is KLHDC8B (Kelch Domain Containing 8B), and among its related pathways/superpathways are miRNAs involved in DNA damage response and ncRNAs involved in STAT3 signaling in hepatocellular carcinoma. The drugs Miconazole and Clotrimazole have been mentioned in the context of this disorder. Affiliated tissues include Blood, and related phenotypes are fatigue and immunodeficiency

Common Targets
GSTP1 | JAK1 | CHEK2 | HLA-DQB1 | G596 | LOC105379570 | ISLR | BRME1 | CRBN | DLEC1 | PVT1 | PDE4D | DECR2 | CSNK1E | LOC105379648 | MAP3K12 | CYP3A4 | TCF3 | LOC105379652 | MEGF11 | PSMB5 | LOC105379658 | JAK2 | IL1B | TM7SF3 | EOMES | PTPRD | LGI4 | MYD88 | G2335 | G3569 | GATA3-AS1 | MAGEC1 | HDAC6 | RTN4RL2 | HCP5 | ACSM3 | HDAC2 | BTK | Heat shock protein 90 (nonspecified subtype) | CPLANE1 | ESYT3 | SLC18A3 | ELANE | ATP13A5 | SHANK2 | IL2RA | NPM1 | CHEK1 | Protein Kinase B (PKB/Akt) (nonspecified subtype) | HLA class II histocompatibility antigen, DRB1-7 beta chain, transcript variant X1 | NF-kappaB (NFkB) | PIGU | Phosphatidylinositol 3-kinase (PI3K) (nonspecified subtype) | ACE | LAG3 | LPP | BMX | Ribonucleoside-diphosphate reductase | GSTA1 | Protein kinase C (nonspecified subtype) | G5133 | G598 | CSF1R | ERI2 | mTOR complex 1 | IL4R | HLA-G | KIT | G29126 | HLA-B | LOC105375755 | IL3RA | MYOD1 | ATP13A5-AS1 | RHOH | UPF3A | HLA-DRB1 | PIK3CD | NFKBIA | DNA Topoisomerase II (nonspecified subtype) | BLMH | TUBB6 | HDAC3 | XPO1 | DLK1 | CD40 | ZNF526 | NCOA5 | ABCC2 | G1029 | ITK | SYK | TSLP | GPC1 | HDAC1 | TINF2 | MAP4K1 | SUMO activating enzyme complex | FCGR3A | FCGBP | PRF1 | KRT39 | HLA-A | G9429 | BCL2A1 | DCX (DDB1-CUL4-X-box) E3 protein ligase complex | G2475 | MS4A1 | PRKDC | XPO5 | mTOR complex 2 | CHAT | HCG9 | KIF11 | ERCC2 | STAB1 | DOCK3 | CD80 | Histocompatibility antigen-related | SERPINF2 | G836 | RAD51 | EEF1A2 | AOPEP | CLEC16A | BCL2L2 | NR3C1 | BLK | OPN1SW | PTPN22 | FCGR2A | PON1 | TNXB | PRR12 | MAGI1 | Tubulin | LOC105370003 | CD79B | TLR9 | MIR146A | EPHX1 | VDR | NAMPT | TNFRSF8 | SH3BP2 | CTLA4 | KIF16B | CACNA1I | IFNG | PIK3CA | GATA3 | TSBP1 | PGRMC1 | ARHGEF28 | MIF | CDCP2 | G7124 | NQO1 | VSIR | UGT1A1 | FLT3 | DHFR | PTPRC | IL10 | IL6R | MIR196A2 | MGMT | Proteasome Complex | IL4 | Histone deacetylase (nonspecified subtype) | RHOA | TOGARAM1 | G5243 | Ferritin | ZNF823 | IGSF11 | TEX55 | IL13 | CD19 | POU2AF1 | AHI1 | CALU | G238 | NSRP1

疾病靶点研报
Hodgkin Lymphoma

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

Other Diseases

Prader-Willi Syndrome | Cantu Syndrome | Fibronectin Glomerulopathy | Osteonecrosis | PHARC Syndrome | Intermittent Claudication | Basan Syndrome | Glioblastoma Multiforme | Sarcoidosis | Basal Ganglia Disease, Biotin-responsive | Aplastic Anemia | Dyggve-Melchior-Clausen Disease | DNA Ligase IV Deficiency | Progressive Familial Intrahepatic Cholestasis Type 3 | Paget's Disease Of The Breast | C3 Glomerulonephritis | Spinal Muscular Atrophy With Progressive Myoclonic Epilepsy | CHARGE Syndrome | Treacher Collins Syndrome | Orthostatic Intolerance | Congenital Central Hypoventilation Syndrome | Down Syndrome | Ependymoma | Pulmonary Capillary Hemangiomatosis | Hypokalemic Periodic Paralysis | Pemphigoid | Tay-Sachs Disease | Charcot-Marie-Tooth Disease Type 4B1 | ICF Syndrome | Chondromyxoid Fibroma | Asthma, Exercise-induced | Acute Leukemia | Vitamin A Deficiency | Carbonic Anhydrase VA Deficiency | Rett Syndrome | Atherosclerosis | AIDS | Hypercholesterolemia | Pseudohypoparathyroidism Type 1B | Hemorrhoids | Imerslund-Grasbeck Syndrome | Fibrodysplasia Ossificans Progressiva | Blue Nevus | Early Infantile Epileptic Encephalopathy | Chronic Myeloid Leukemia | Snyder-Robinson Syndrome | Carcinoma, Signet Ring Cell | Pseudohypoaldosteronism | Intracranial Hypertension | Conn Syndrome | Chronic Granulomatous Disease, X-linked | Juvenile Hyaline Fibromatosis | Sclerocornea | Hartnup Disease | H Syndrome | Charcot-Marie-Tooth Disease Type 4D | Osteoporosis-pseudoglioma Syndrome | Pure Autonomic Failure | Sleep Apnea, Obstructive | Pearson Syndrome | Maternally Inherited Diabetes And Deafness | Hyperphenylalaninemia | Carbamoyl Phosphate Synthetase I Deficiency | Cardiac Arrest | Neuroendocrine Cancer | Autoimmune Polyendocrine Syndrome | LRBA Deficiency | COACH Syndrome | Hypertension, Portal | CDKL5 Deficiency Disorder | Meckel-Gruber Syndrome | Hypothalamic Obesity | Steel Syndrome | Pulmonary Alveolar Microlithiasis | Hyperbilirubinemia | Spondyloarthritis | Hepatitis C, Chronic | Nephrotic Syndrome Type 1 | Spinocerebellar Ataxia Type 15 | Cataplexy | Hairy Cell Leukemia | Hemangioendothelioma | CHOPS Syndrome | Lymphoma, Primary Cutaneous Anaplastic Large Cell | Esotropia | Hereditary Pyropoikilocytosis | Tricho-hepato-enteric Syndrome | Nutrition Disorders | Spinocerebellar Ataxia Type 12 | Cystinuria | Disseminated Superficial Actinic Porokeratosis | Chondrodysplasia Punctata 2, X-linked Dominant | Hamartoma | Avellino Corneal Dystrophy | Epidermolysis Bullosa Simplex, Dowling-Meara Type | Osteosclerosis | Emery-Dreifuss Muscular Dystrophy | ACTH-independent Macronodular Adrenal Hyperplasia | Anorchia | Budd-Chiari Syndrome | Prolymphocytic Leukemia | Pierre Robin Syndrome | Neonatal Progeroid Syndrome | Hypertension | Neurofibroma | Inflammatory Joint Disease | Mitochondrial Myopathy | Thanatophoric Dysplasia | Leukoencephalopathy, Progressive Multifocal | Waldenstrom Macroglobulinemia | Osteogenesis Imperfecta Type II | Polycythemia | Amebiasis | Niemann-Pick Disease, Type C | Megaloblastic Anemia | Hypercalcemia | Chitayat Syndrome | Epilepsy Of Infancy With Migrating Focal Seizures | Porphyria, Variegate | Ganglioglioma | Rickets | Glutathione Synthetase Deficiency | Familial Cerebral Amyloid Angiopathy | Lennox-Gastaut Syndrome | Thrombotic Microangiopathy | Cancer, Brain | Hermansky-Pudlak Syndrome | Myoclonus-dystonia Syndrome | Acrodermatitis | Beckwith-Wiedemann Syndrome | Inflammatory Myopathy | Dwarfism | Autism | Conjunctivitis, Allergic | Leiomyoma | Superficial Spreading Melanoma | Ulcerative Colitis | Duane Retraction Syndrome | Papillon-Lefevre Syndrome | Major Depression | Osteogenesis Imperfecta Type VI | Aldosterone Deficiency | Prediabetes | Leri-Weill Dyschondrosteosis | Waardenburg Syndrome Type 2A | Leishmaniasis, Cutaneous | Avian Influenza | Myasthenia Gravis | Amish Infantile Epilepsy Syndrome | Ventricular Septal Defect | Hypoalbuminemia | Hereditary Mixed Polyposis Syndrome | Chronic Granulomatous Disease | Proopiomelanocortin Deficiency | Cirrhosis | Leishmaniasis, Visceral | Osteogenesis Imperfecta Type III | Cryptosporidiosis | Progressive Familial Intrahepatic Cholestasis Type 1 | Mitochondrial DNA Depletion Syndrome, Encephalomyopathic Form | Branchiootorenal Syndrome | Scleroderma, Diffuse | Pelizaeus-Merzbacher Disease | Encephalopathy | Acute Lung Injury | Retinitis | Sotos Syndrome | Hypersensitivity | Fatty Aldehyde Dehydrogenase Deficiency | Aceruloplasminemia | Placenta Previa | Antiphospholipid Syndrome | Neuroma | Parapsoriasis | Pycnodysostosis | Fraser Syndrome | Myosin Storage Myopathy | Cutaneous Angiosarcoma | Antisynthetase Syndrome | Cholestasis, Intrahepatic | Aspergillosis | Gastritis | 6-pyruvoyl-tetrahydropterin Synthase Deficiency | Anodontia | Thyroid Hormone Resistance | Pancreatitis, Chronic | Brenner Tumor | Tendinitis | Fabry's Disease | Metachondromatosis | Rhizomelic Chondrodysplasia Punctata | Amyloidosis | Spinocerebellar Ataxia Type 20 | Charcot-Marie-Tooth Disease Type 4E | Charcot-Marie-Tooth Disease Type 2D | Neurofibromatosis | Anorectal Fistula | Autoimmune Hemolytic Anemia | Ectopia Lentis, Isolated, Autosomal Recessive | McKusick Type Metaphyseal Chondrodysplasia | Tyrosinemia | Fucosidosis | Kaposi Sarcoma | Mucormycosis | Cardiospondylocarpofacial Syndrome | Leukoplakia | Auriculocondylar Syndrome | Postpoliomyelitis Syndrome | Cherubism | Focal Facial Dermal Dysplasia | Carcinoid Tumor | Distal Spinal Muscular Atrophy | Psoriasis | Subacute Sclerosing Panencephalitis | Thalassemia | Dermatitis Herpetiformis | Pitt-Hopkins Syndrome | Krabbe Disease | Angelman Syndrome | Primary Aldosteronism | Botulism | Hereditary Elliptocytosis | Chronic Mucocutaneous Candidiasis | Proteasome-associated Autoinflammatory Syndrome 2 | Primary Carnitine Deficiency | Celiac Disease | Isovaleric Acidemia | Oculocutaneous Albinism Type 4 | D-2-Hydroxyglutaric Aciduria | Microcephalic Osteodysplastic Primordial Dwarfism, Type II | Aldosterone Synthase Deficiency | Panniculitis | Fibrosarcoma | Non-bullous Congenital Ichthyosiform Erythroderma | Woodhouse-Sakati Syndrome | Keratoconjunctivitis | Joubert Syndrome | Epidermolysis Bullosa Dystrophica | Bronchiectasis | Antithrombin III Deficiency | Papilloma | Lymphopenia | Haim-Munk Syndrome | Diabetic Nephropathy | Left Ventricular Noncompaction | Adenoid Cystic Carcinoma | Charcot-Marie-Tooth Disease Type 3 | Focal Segmental Glomerulosclerosis | Martsolf Syndrome | Basal Cell Nevus Syndrome | Vascular Cognitive Impairment | Nephropathy | Creatine Deficiency Syndrome Due To AGAT Deficiency | Dominant Optic Atrophy | Lupus Erythematosus | Incontinentia Pigmenti | Dysthymia | Prune Belly Syndrome | Hidradenitis Suppurativa | Netherton Syndrome | Lamellar Ichthyosis | Neuronal Ceroid Lipofuscinosis | Ichthyosis | Familial Glucocorticoid Deficiency | Cerebral Amyloid Angiopathy | Facioscapulohumeral Muscular Dystrophy Type 1 | Spinocerebellar Ataxia Type 1 | Fetal Akinesia Deformation Sequence | Clouston Hidrotic Ectodermal Dysplasia | Malnutrition | Hypokalemia | Lentigo | Myositis, Focal | Mumps | Headache | Hemimegalencephaly | Hyperhomocysteinemia | VEXAS Syndrome | Primary Ovarian Insufficiency | T-cell Prolymphocytic Leukemia | Otopalatodigital Syndrome Type 2 | Schwannomatosis | Acute Generalized Exanthematous Pustulosis | Vitreoretinal Degeneration, Snowflake Type | Congenital Fiber-type Disproportion Myopathy | Hypotension, Orthostatic | 3-methylcrotonyl-CoA Carboxylase Deficiency | Myopia | Mosaic Variegated Aneuploidy Syndrome 2 | Monilethrix | Vitamin K Deficiency | Cerebellofaciodental Syndrome | Dysgerminoma | Usher Syndrome Type I | Hypophosphatasia | Wolfram Syndrome 2 | McCune-Albright Syndrome | NGLY1 Deficiency | Reflex Epilepsy | Eosinophilia | Early Infantile Epileptic Encephalopathy 13 | Pneumonia, Mycoplasma | Cholecystitis | Primary Hyperoxaluria Type 3 | Schnyder Crystalline Corneal Dystrophy | Methylmalonic Aciduria And Homocystinuria, CblC Type | Acne Vulgaris | Thyroiditis, Autoimmune | Congestive Heart Failure | FG Syndrome | Familial Exudative Vitreoretinopathy | Colon Adenoma | Endophthalmitis | Hydrolethalus Syndrome | Dysmorphophobia | Autosomal Recessive Spastic Paraplegia Type 35 | Myotonia | Lymphoma | Uremia | Spinocerebellar Ataxia Type 42 | Juvenile Polyposis | Tonsillitis | Gingivitis | Carpal Tunnel Syndrome | Pseudomyxoma Peritonei | Peritonitis | Melanocytic Nevus | Inflammatory Bowel Disease | T-cell Leukemia | Anal Fissure | Mastitis | Scabies | Infantile Liver Failure Syndrome 1 | Neuroleptic Malignant Syndrome | Congenital Muscular Dystrophy | Osteogenesis Imperfecta | Gilbert Syndrome | Lymphoproliferative Disorders | Hepatopulmonary Syndrome | Glycogen Storage Disease Type 1a | Congenital Hemolytic Anemia | Thrombasthenia | Sulfite Oxidase Deficiency | Ichthyosis, X-linked | Lymphangioma | Alveolar Capillary Dysplasia | Argininosuccinic Aciduria | Spondylosis | Hyperparathyroidism, Primary | Necrobiosis Lipoidica | MELAS Syndrome | Polymyalgia Rheumatica | Fuchs Heterochromic Iridocyclitis | Sertoli Cell-only Syndrome | Thyrotoxic Periodic Paralysis | Atopic Dermatitis | Huntington's Disease | Alpha-thalassemia Myelodysplasia Syndrome | Metanephric Adenoma | Priapism | Neurodermatitis | Hereditary Coproporphyria | Macular Corneal Dystrophy | Tumoral Calcinosis | Beta-Propeller Protein-associated Neurodegeneration | Liebenberg Syndrome | Ehlers-Danlos Syndrome | Frontometaphyseal Dysplasia | Hyperparathyroidism, Secondary | Swine Influenza | Spinal Cord Diseases | Usher Syndrome | Sepiapterin Reductase Deficiency | Riboflavin Transporter Deficiency Neuronopathy | Scleroderma | Seasonal Mood Disorder | Trichomegaly | Leukocyte Adhesion Deficiency Type 1 | Epidermolysis Bullosa Simplex | Reye Syndrome | Allan-Herndon-Dudley Syndrome | Tenosynovial Giant Cell Tumor | Pulmonary Veno-occlusive Disease | Pulmonary Vein Stenosis | Spondylo-ocular Syndrome | Deafness, Dystonia, And Cerebral Hypomyelination | Diverticulitis | Arterial Tortuosity Syndrome | Plasma Cell Dyscrasia | Seizures-scoliosis-macrocephaly Syndrome | Optic Nerve Diseases | Multiple Sclerosis, Relapsing-remitting | Genee-Wiedemann Syndrome | Spinocerebellar Ataxia Type 31 | Schizophrenia, Paranoid | Renal Hypouricemia | Spinocerebellar Ataxia Type 2 | Hemorrhagic Disorders | Pterygium | Waardenburg Syndrome Type 4A