Disease

Cutaneous T-cell Lymphoma

About the Disease
Primary Cutaneous T-Cell Non-Hodgkin Lymphoma, also known as cutaneous t-cell lymphoma, is related to primary cutaneous gamma-delta t-cell lymphoma and parapsoriasis. An important gene associated with Primary Cutaneous T-Cell Non-Hodgkin Lymphoma is TNFRSF8 (TNF Receptor Superfamily Member 8), and among its related pathways/superpathways are Innate Immune System and ERK Signaling. The drugs Levoleucovorin and Methotrexate have been mentioned in the context of this disorder. Affiliated tissues include t cells, skin and bone marrow, and related phenotypes are no effect and no effect

Common Targets
TRBC1 | Histone deacetylase (nonspecified subtype) | KIR3DL2 | Proteasome Complex | ITGAM | PASK | G5243 | LPL | TLR7 | PIK3CG | G7124 | Tumor-Associated Glycoprotein 72 (TAG-72) | IL6ST | JAK3 | JAK1 | PSMB5 | HDAC10 | G596 | IL-15 receptor | G3845 | TLR8 | CD6 | TNFRSF1B | KCNA3 | Geranylgeranyl transferase type-1 | JAK2 | G5594 | Interferon-gamma Receptor | G6774 | HDAC6 | DNMT3A | HDAC2 | HIF1A | MIR155 | CARD11 | NRAS | CCR4 | SOCS5 | MAP3K5 | IL2RA | G3569 | GLI3 | FKBP1A | PAK5 | CD79A | TRAF6 | G598 | Phosphatidylinositol 3-kinase (PI3K) (nonspecified subtype) | Protein kinase C (nonspecified subtype) | G5133 | CD3 Complex (T Cell Receptor Complex) | HDAC11 | NF-kappaB (NFkB) | G29126 | IL-2 receptor | FLNA | ABCA1 | IL15 | HDAC3 | SIRPA | DNA Topoisomerase II (nonspecified subtype) | PIK3CD | STAT5 (nonspecified subtype) | RC3H1 | HDAC1 | SATB1 | SYK | G3605 | FCGR3A | G920 | Interferon (nonspecified subtype) | ACHE | Immunoglobulin E (IgE) | PPARG | PNP | PLCG1 | BCOR | NCR3 | IL17F | IL31 | G2475 | NLRP2 | SPI1 | RARB | G3630 | RELB | G836 | HK2 | Mitogen-Activated Protein Kinase (nonspecified subtype) | RB1 | POLA1 | PIM1 | Janus Kinase (nonspecified subtype) | G7157 | TNFRSF8 | NAMPT | Retinoid RXR receptor (nonspecified subtype) | CD37 | FCER1A | FAS | TLR9 | CD47 | Tubulin | CD28 | RARG | IL9R | Mitogen-activated protein kinase (JNK) (nonspecified subtype) | LRRC43 | MGMT | DHFR | VHL | RHOA | IFNAR2 | TOP2A

疾病靶点研报
Cutaneous T-cell Lymphoma

Note: If you'd like to get a target analysis report for Cutaneous T-cell 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 Cutaneous T-cell Lymphoma at a cost 90% lower than traditional approaches, please feel free to contact us at BD@silexon.ai.

Other Diseases

Hyperparathyroidism, Secondary | Mucolipidosis Type III | Intestinal Hypomagnesemia 1 | Congenital Myopathy | Antithrombin III Deficiency | Klippel-Feil Syndrome | Hepatitis, Autoimmune | Blepharophimosis Syndrome | Blepharospasm | Benign Familial Infantile Seizures | Lymphoma, B-cell | Leukocyte Adhesion Deficiency | Anti-glomerular Basement Membrane Disease | Snyder-Robinson Syndrome | Ocular Albinism Type 1 | Ehlers-Danlos Syndrome | Nicotine Dependence | Varices | Dermatofibrosarcoma | Acne | Batten Disease | Congenital Dysfibrinogenemia | Silver-Russell Syndrome | Pierre Robin Syndrome | Muir-Torre Syndrome | Spinocerebellar Ataxia Type 16 | Craniofacial Dysostosis | Ameloblastic Carcinoma | Hyperhomocysteinemia | Esophageal Adenocarcinoma | WAGR Syndrome | Coronary Artery Disease | Hyperinsulinism-hyperammonemia Syndrome | Cardiomyopathy, Hypertrophic | Pneumothorax | Focal Segmental Glomerulosclerosis | Hypercalciuria | Keloid | Primary Carnitine Deficiency | Agammaglobulinemia | Porokeratosis | Porphyria, Acute Intermittent | Autoimmune Polyendocrinopathy Syndrome Type I | Pyruvate Carboxylase Deficiency Disease | Lymphoproliferative Disease, X-linked | Bruck Syndrome | Distal Spinal Muscular Atrophy | Esotropia | Schizencephaly | Hypohidrotic Ectodermal Dysplasia, X-linked | Postaxial Polydactyly | Polyradiculopathy | Congenital Absence Of Vas Deferens | Rhabdomyosarcoma | Sick Sinus Syndrome | Thrombophlebitis | Large Granular Lymphocytic Leukemia | Niemann-Pick Disease, Type C | Neovascular Glaucoma | Spinocerebellar Ataxia Type 38 | Osteogenesis Imperfecta Type I | Majeed Syndrome | Neurocutaneous Melanocytosis | Hepatic Steatosis | Spinocerebellar Ataxia Type 8 | Depression | Glutathione Synthetase Deficiency | Cryptococcal Meningitis | Fontaine Progeroid Syndrome | Cutaneous Mastocytosis | Primary Hyperoxaluria Type 3 | Epidermolysis Bullosa Dystrophica | Lamellar Ichthyosis | Stargardt Disease | Hypertension | Methylmalonic Aciduria And Homocystinuria, CblC Type | Myeloid Leukemia | Malonyl-CoA Decarboxylase Deficiency | Gerodermia Osteodysplastica | Scabies | Bulimia Nervosa | Ehlers-Danlos Syndrome With Progressive Kyphoscoliosis, Myopathy, And Hearing Loss | Cerebellar Ataxia, Cayman Type | Sialoadenitis | Double Outlet Right Ventricle | Myasthenia Gravis | Ophthalmoplegia | Niemann-Pick Disease | Gardner Syndrome | Addison Disease | Synpolydactyly | Veno-occlusive Disease | Raine Syndrome | Adrenoleukodystrophy, X-linked | Gastroenteritis | Postpoliomyelitis Syndrome | Knobloch Syndrome | Acrodermatitis Enteropathica | Cataplexy | Gallstones | Keratosis, Seborrheic | Diabetic Neuropathy | Fetal Akinesia Deformation Sequence | Spondylo-megaepiphyseal-metaphyseal Dysplasia | Plasmacytoma | Dyslipidemia | Pitt-Hopkins Syndrome | 3-hydroxy-3-methylglutaryl-CoA Synthase Deficiency | Facioscapulohumeral Muscular Dystrophy Type 1 | Hereditary Pyropoikilocytosis | Mohr-Tranebjaerg Syndrome | Traboulsi Syndrome | Lymphopenia | Mevalonate Kinase Deficiency | Blue Nevus | Multiple Sulfatase Deficiency | Micropenis | Carpal Tunnel Syndrome | Hereditary Sensory Neuropathy Type 1 | Bartter Syndrome | Schizophrenia, Paranoid | Acute Lymphocytic Leukemia | Polycystic Kidney, Autosomal Recessive | Renal Tubular Dysgenesis | Macular Corneal Dystrophy | Pulmonary Veno-occlusive Disease | Angelman Syndrome | Thromboembolism | Charcot-Marie-Tooth Disease, Type 2A | Angioedema | Parkinsonism | Ichthyosis Hystrix, Curth-Macklin Type | Methylmalonic Acidemia | Chronic Mucocutaneous Candidiasis | Neuropathy | Blastoma, Pleuropulmonary | Greenberg Dysplasia | Uterine Leiomyoma | Stroke, Hemorrhagic | Tenosynovial Giant Cell Tumor | Sarcomatoid Carcinoma Of The Lung | X-linked Myotubular Myopathy | Wiedemann-Steiner Syndrome | Colon Adenoma | Central Retinal Artery Occlusion | Pure Autonomic Failure | CDKL5 Deficiency Disorder | Papilledema | Osteogenesis Imperfecta Type II | Intellectual Disability, Autosomal Dominant 5 | Atelosteogenesis Type 2 | Maternally Inherited Diabetes And Deafness | Autonomic Neuropathy | Colitis, Lymphocytic | Stomatitis | Pernicious Anemia | Proopiomelanocortin Deficiency | Pre-eclampsia | Mandibuloacral Dysplasia With Type A Lipodystrophy | Tay-Sachs Disease | Retinal Coloboma | Sclerocornea | Ganglioglioma | Otitis Media | Achromatopsia | Pyruvate Decarboxylase Deficiency | Encephalitis | Spondylolisthesis | Progressive External Ophthalmoplegia | LRBA Deficiency | Major Depression | Microphthalmia, Syndromic 7 | Cornelia De Lange Syndrome | Asthma | Pemphigoid | Dubin-Johnson Syndrome | Anorchia | Niemann-Pick Disease, Type A | Metabolic Syndrome | Cardiomyopathy, Restrictive | Schnyder Crystalline Corneal Dystrophy | CHOPS Syndrome | Thalassemia, Beta | Carcinoma In Situ | Oculocutaneous Albinism Type 1 | Cerebrovascular Disorders | Myocarditis | Disseminated Intravascular Coagulation | Takenouchi-Kosaki Syndrome | Celiac Disease | Neutropenia | Cholangiocarcinoma | Tendinopathy | Vitamin A Deficiency | Corticobasal Syndrome | Low Phospholipid Associated Cholelithiasis | Branchiootorenal Syndrome | Juvenile Polyposis | Gyrate Atrophy Of The Choroid And Retina | Hydronephrosis | Ataxia-hypogonadism-choroidal Dystrophy Syndrome | Thrombocythemia, Essential | Carney Triad | MELAS Syndrome | Retinal Telangiectasia | Renal Hypouricemia | Pemphigus Vulgaris | Nemaline Myopathy 10 | Anencephaly | Lymphangioleiomyomatosis | Carbohydrate Metabolism Disorders | Shwachman-Bodian-Diamond Syndrome | Hemochromatosis | Monilethrix | Retinitis | Neuronal Ceroid Lipofuscinosis | Acute Tubular Necrosis | Japanese Encephalitis | Fibronectin Glomerulopathy | Hypertriglyceridemia | Meier-Gorlin Syndrome | Astigmatism | Anorectal Malformations | Sarcoma, Alveolar Soft Part | Amelogenesis Imperfecta | Syncope | Epidermolysis Bullosa Simplex, Dowling-Meara Type | Melanoma, Malignant | Prune Belly Syndrome | Pupil Disorders | Myocardial Infarction | Enhanced S-cone Syndrome | Congenital Poikiloderma | Heroin Dependence | Demyelinating Diseases | Cardiomyopathy, Dilated, 1L | Meleda Disease | Hypoalbuminemia | Sepiapterin Reductase Deficiency | Biotinidase Deficiency | Cardiac Arrest | Borderline Personality Disorder | Aarskog-Scott Syndrome | Carcinoma, Squamous Cell | Camurati-Engelmann Disease | Trichothiodystrophy | Acute Lung Injury | Occipital Neuralgia | Congenital Afibrinogenemia | Sertoli Cell-only Syndrome | Neuromyotonia | Long QT Syndrome Type 2 | Paroxysmal Nocturnal Hemoglobinuria | Aicardi-Goutieres Syndrome | Speech Disorders | Nasodigitoacoustic Syndrome | Melanocytic Nevus | Angiodysplasia | Hernia, Inguinal | Heart Failure | Eczema | Anuria | Glutaric Aciduria Type 2 | Neurogenic Bladder | Prediabetes | Mitochondrial Disease | Spinal Cord Diseases | Birk-Barel Syndrome | Diabetes Insipidus | Treacher Collins Syndrome | Prurigo Nodularis | Proctitis | DNA Ligase IV Deficiency | Bardet-Biedl Syndrome | Tinea Versicolor | X-linked Sideroblastic Anemia | Hereditary Mixed Polyposis Syndrome | Arterial Tortuosity Syndrome | Epidermodysplasia Verruciformis | Glucagonoma | Cutaneous T-cell Lymphoma | Primary Progressive Aphasia | Transcobalamin Deficiency | Primary Pigmented Nodular Adrenocortical Disease | Congenital Bile Acid Synthesis Defect | Atelosteogenesis Type 1 | Acute Generalized Exanthematous Pustulosis | Primary Torsion Dystonia | Polycystic Kidney, Autosomal Dominant | Relapsing Polychondritis | Common Variable Immunodeficiency | Osteonecrosis Of The Jaw | Holt-Oram Syndrome | Congenital Disorders Of Glycosylation | Infertility, Male | Wolfram Syndrome | Inflammatory Linear Verrucous Epidermal Nevus | Carotid Artery Disease | Coloboma | Teratozoospermia | Familial Retinal Arterial Macroaneurysm | Melnick-Needles Syndrome | Skin Fragility-woolly Hair Syndrome | Hereditary Sensory And Autonomic Neuropathy | Usher Syndrome | Exfoliative Dermatitis | Megaloblastic Anemia | Hypertension, Portal | Cerebral Amyloid Angiopathy | Poikiloderma With Neutropenia | Proximal Symphalangism | Membranous Nephropathy | Arthritis, Psoriatic | Seminoma | Pelizaeus-Merzbacher Disease | Adenomyosis | Hyperprolactinemia | Tyrosine Hydroxylase Deficiency | Congenital Diaphragmatic Hernia | Bone Marrow Necrosis | DiGeorge Syndrome | Acute Kidney Injury | Autoimmune Disease | Neurodevelopmental Disorder With Central Hypotonia And Dysmorphic Facies | Craniofrontonasal Syndrome | Phenylketonuria | Congestive Heart Failure | Hyperbilirubinemia | Mitochondrial DNA Depletion Syndrome, Hepatocerebral Form | Pain | Trachoma | Retinal Detachment | DOCK8 Immunodeficiency Syndrome | Angioedema, Hereditary | Granular Corneal Dystrophy Type 1 | Chorea-acanthocytosis | Usher Syndrome Type IIC | Hypoglycemia | Epidermolysis Bullosa Simplex | Spinocerebellar Ataxia Type 12 | Inflammatory Myopathy | Zollinger-Ellison Syndrome | Thrombophilia | Antiphospholipid Syndrome | Dystonia-parkinsonism, X-linked | Liver Failure, Acute Infantile | Immunoproliferative Disorders | Fowler's Syndrome | Glycogen Storage Disease Type 3 | Myelofibrosis | Leukemia | Juvenile Myelomonocytic Leukemia | Bleeding Disorder Due To CalDAG-GEFI Deficiency | Pierpont Syndrome | Otopalatodigital Syndrome Type 2 | Mast Cell Leukemia | Fragile X Syndrome | Trichotillomania | Steel Syndrome | Progressive Osseous Heteroplasia | Gangliosidosis, GM1 | Cat Eye Syndrome | Lymphoma Lymphoblastic | Meningitis | Hypotension, Orthostatic | Pyelonephritis | Pemphigus Foliaceus | Bursitis | Pemphigus | Chronic Beryllium Disease | Erdheim-Chester Disease | Asperger Syndrome | Binge Eating Disorder | Pineoblastoma | Microphthalmia | Reflex Epilepsy | Guillain-Barre Syndrome | Malaria | Amyotrophic Lateral Sclerosis, Juvenile | Multicystic Renal Dysplasia | ACTH-independent Macronodular Adrenal Hyperplasia | Neurodermatitis | Optic Nerve Diseases | Osteonecrosis | Ameloblastoma | Carcinoma, Transitional Cell | Familial Pheochromocytoma-paraganglioma | Parvovirus B19 Infection | Keratoacanthoma | Focal Facial Dermal Dysplasia | Hypotonia-cystinuria Syndrome | Pseudoexfoliation Syndrome | Neuromyelitis Optica | Wiskott-Aldrich Syndrome | Panuveitis | Neurofibromatosis Type 2 | Harlequin Ichthyosis | Multiple Congenital Anomalies-hypotonia-seizures Syndrome 2 | Malignant Fibrous Histiocytoma | Pancytopenia