Parapsoriasis

About the Disease
Parapsoriasis, also known as parapsoriasis en plaques, is related to primary cutaneous t-cell non-hodgkin lymphoma and pityriasis rosea. An important gene associated with Parapsoriasis is TNFRSF8 (TNF Receptor Superfamily Member 8), and among its related pathways/superpathways are Innate Lymphoid Cells Differentiation and Network map of SARS-CoV-2 signaling pathway. The drugs Apremilast and Thalidomide have been mentioned in the context of this disorder. Affiliated tissues include skin, t cells and lymph node.

Common Targets
G3605 | IFNG | IL4

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

Other Diseases

Ocular Surface Squamous Neoplasia | Kohlschutter-Tonz Syndrome | Spinocerebellar Ataxia Type 5 | McKusick Type Metaphyseal Chondrodysplasia | Prolidase Deficiency | Osteogenesis Imperfecta Type IV | Jalili Syndrome | Insulinoma | Pleurisy | Steel Syndrome | Dementia | Focal Segmental Glomerulosclerosis | Coronary Restenosis | Congenital Stationary Night Blindness | Blood Protein Disorders | Familial Hyperaldosteronism | Urea Cycle Disorder | Diabetic Macular Edema | Endometritis | Primary Progressive Aphasia | Neuroendocrine Cancer | Narcolepsy | Parkinson's Disease | Vitamin D Deficiency | Sensorineural Hearing Loss | Renal Failure | Nutrition Disorders | Hennekam Lymphangiectasia-lymphedema Syndrome | Myeloid Leukemia | Guanidinoacetate Methyltransferase Deficiency | Joubert Syndrome | Perry Syndrome | Hyperlipidemia | Acute Lymphocytic Leukemia | Anterior Segment Dysgenesis | Cholecystitis | Acute Kidney Injury | Diastrophic Dysplasia | Meleda Disease | Aceruloplasminemia | Neurodegeneration With Brain Iron Accumulation | Connective Tissue Disorders | Inflammatory Myofibroblastic Tumor | Bleeding Disorder Due To CalDAG-GEFI Deficiency | Olmsted Syndrome | Canavan Disease | Hairy Cell Leukemia | Alopecia Areata | Amyotrophic Lateral Sclerosis | Atopic Dermatitis | Optic Neuropathy, Anterior Ischemic | Temporal Lobe Epilepsy | Bronchiolitis | Restless Legs Syndrome | Monilethrix | Infectious Diarrhea | Growth Hormone Excess | Feingold Syndrome | Hyperprolactinemia | Acromesomelic Dysplasia | Ganglioneuroma | Alpers Syndrome | Diffuse Mesangial Sclerosis | Creutzfeldt-Jakob Disease | Stroke, Ischemic | Sjogren Syndrome | Antenatal Bartter Syndrome Type 1 | Mucolipidosis | Autism | Cystitis, Interstitial | Carcinoma, Signet Ring Cell | Blomstrand Osteochondrodysplasia | Cancer, Breast | Sarcoma, Endometrial Stromal | Schnyder Crystalline Corneal Dystrophy | Cyst | Encephalopathy, Ethylmalonic | Polyomavirus Nephropathy | Ameloblastic Carcinoma | Hereditary Inclusion Body Myopathy | Vitiligo | Optic Nerve Diseases | Thyroid Dyshormonogenesis | Colitis | Lymphoma, Mantle Cell | Absence Epilepsy | Tracheal Disorders | IgA Deficiency | Bruck Syndrome | Holt-Oram Syndrome | Cabezas Syndrome | Methylmalonic Acidemia | Nephrotic Syndrome | Thin Basement Membrane Disease | Heroin Dependence | Familial Dysautonomia | Localized Scleroderma | Reye Syndrome | X-linked Sideroblastic Anemia | Osteoporosis | Gangliosidosis, GM1 | Glioblastoma | Corneal Dystrophy And Perceptive Deafness | Hemophagocytic Lymphohistiocytosis | Retinal Diseases | Anemia | Subcortical Band Heterotopia | Nestor-Guillermo Progeria Syndrome | Gastritis | Rubinstein-Taybi Syndrome | Persistent Truncus Arteriosus | Xeroderma Pigmentosum Variant Type | Myelitis | Leigh Syndrome | Nail-Patella Syndrome | Kernicterus | Meconium Ileus | Epidermodysplasia Verruciformis | Lymphopenia | Tylosis With Esophageal Cancer | Cataract | Genee-Wiedemann Syndrome | Fuchs Heterochromic Iridocyclitis | Binge Eating Disorder | Fatty Aldehyde Dehydrogenase Deficiency | Alagille Syndrome | Creatine Deficiency Syndrome Due To AGAT Deficiency | Prediabetes | Neuroleptic Malignant Syndrome | Sepiapterin Reductase Deficiency | Intestinal Obstruction | Thrombosis | Spinocerebellar Ataxia Type 17 | Globozoospermia | Paroxysmal Kinesigenic Dyskinesia | Teratozoospermia | Glutathione Synthetase Deficiency | Irritable Bowel Syndrome | Hypertension, Renal | Intestinal Pseudo-obstruction | Macrophagic Myofasciitis | Sleep Apnea | Infantile Neuroaxonal Dystrophy | Premature Ejaculation | Lymphoma Lymphoblastic | Corneal Neovascularization | Dengue Shock Syndrome | Encephalopathy, Hepatic | Retinopathy Of Prematurity | Cerebrotendinous Xanthomatosis | Niemann-Pick Disease, Type A | Neurofibroma, Plexiform | Cat Eye Syndrome | NDH Syndrome | Cerebral Cavernous Malformations | Hepatic Steatosis | Dentinogenesis Imperfecta | Pneumococcal Meningitis | Myoclonus | Paraganglioma | Noonan Syndrome | Polycystic Ovary Syndrome | Macular Corneal Dystrophy Type 1 | Blastomycosis | Ataxia-ocular Apraxia 2 | Smith-Kingsmore Syndrome | Hypersomnia | Porphyria, Acute Intermittent | Micropenis | Conjunctivitis | Mumps | Neovascular Glaucoma | Stevens-Johnson Syndrome | Intracerebral Hemorrhage | Kleine-Levin Syndrome | Preaxial Polydactyly | Neurofibrosarcoma | Diabetic Nephropathy | Cerebral Amyloid Angiopathy | Albinism | Chordoid Glioma | Geleophysic Dysplasia | Triple A Syndrome | Gastrointestinal Disorders | Glioblastoma Multiforme | Prune Belly Syndrome | Vitamin B12 Deficiency | Autoimmune Hemolytic Anemia | Ischemia | Hypertrophic Osteoarthropathy, Primary, Autosomal Recessive 1 | Hypoparathyroidism | Toxoplasmosis | Pierre Robin Syndrome | Microcephalic Primordial Dwarfism | Hidradenitis Suppurativa | Stickler Syndrome | Trimethylaminuria | Agoraphobia | Fibromyalgia | Conduct Disorder | Spinal Muscular Atrophy Type 2 | Myelodysplasia | Anorectal Fistula | Hyperhomocysteinemia | Carbohydrate Metabolism Disorders | Myhre Syndrome | Primary Lateral Sclerosis | Lymphedema-distichiasis Syndrome | Fahr Disease | Congenital Central Hypoventilation Syndrome | Bronchitis | Congenital Nystagmus | Brenner Tumor | Gaze Palsy, Familial Horizontal, With Progressive Scoliosis, 2 | Tyrosine Hydroxylase Deficiency | Atelosteogenesis Type 1 | Seborrheic Dermatitis | Oligodendroglioma | Waardenburg Syndrome Type 2 | Danon Disease | Infantile Liver Failure Syndrome 1 | Nevus | Lathosterolosis | Tonsillitis | Primary Torsion Dystonia | Facioscapulohumeral Muscular Dystrophy Type 2 | Optic Atrophy 2 | Granular Corneal Dystrophy Type 1 | 3C Syndrome | Acrodermatitis Enteropathica | Porphyria Cutanea Tarda | Sarcoidosis, Pulmonary | Autosomal Recessive Spastic Paraplegia Type 35 | Charcot-Marie-Tooth Disease, Type 2A | Hashimoto Thyroiditis | Lymphoma | Ulcerative Colitis | Nephropathy | Influenza | Paronychia | Hepatitis, Chronic | Benign Hereditary Chorea | Guillain-Barre Syndrome | Hypothalamic Obesity | Arts Syndrome | Cancer, Bladder | Ichthyosis Hystrix, Curth-Macklin Type | Von Willebrand Disease | Optic Neuritis | Diabetes Insipidus, Neurogenic | 3-methylglutaconic Aciduria Type I | Coffin-Siris Syndrome | Rosacea | Glomerulonephritis | Osteogenesis Imperfecta Type V | Bainbridge-Ropers Syndrome | Schwannomatosis | Botulism | Venous Insufficiency | Chronic Myelomonocytic Leukemia | Adenomatoid Tumor | Schistosomiasis | Sarcosinemia | Neurodevelopmental Disorder With Central Hypotonia And Dysmorphic Facies | Long QT Syndrome Type 1 | Wolman Disease | Spinocerebellar Ataxia Type 15 | Clouston Hidrotic Ectodermal Dysplasia | Sick Sinus Syndrome | Megalencephaly | Colitis, Microscopic | Galactosemia | Spondylosis | Neurofibromatosis Type 1 | Tendinopathy | Mitochondrial Cytopathy | Keratosis | Pseudohermaphroditism | CHOPS Syndrome | Pemphigoid | Membranous Nephropathy | Li-Fraumeni Syndrome | Congestive Heart Failure | Thalassemia, Beta | Pneumonia, Bacterial | Kaposi Sarcoma | Epicondylitis | Saul-Wilson Syndrome | Micro Syndrome | Oculocutaneous Albinism | Arterial Tortuosity Syndrome | Rift Valley Fever | Rheumatoid Arthritis | Chronic Periodontitis | Common Cold | Barakat Syndrome | Myocardial Infarction | Non-epidermolytic Palmoplantar Keratoderma | Diabetes Insipidus, Nephrogenic | Spinocerebellar Ataxia Type 10 | Rubeosis Iridis | Lymphoma, Follicular | Waardenburg Syndrome Type 2E | Hypersensitivity | Vertebrobasilar Insufficiency | Pseudohypoparathyroidism Type 1A | Tyrosinemia Type 1 | Leukodystrophies | Familial Hypobetalipoproteinemia | Pulverulent Zonular Cataract | Joubert Syndrome 2 | Cardiomyopathy, Dilated, 1L | Charcot-Marie-Tooth Disease, Type 2C | Mitochondrial Encephalomyopathy | Ornithine Transcarbamylase Deficiency | Thrombocythemia, Essential | Gastritis, Atrophic | Hepatitis A | Erythrokeratodermia Variabilis | Menkes Disease | HANAC Syndrome | Sezary Syndrome | Early Infantile Epileptic Encephalopathy 1 | Sitosterolemia | C3 Glomerulopathy | Sleep Apnea, Central | Angioedema, Acquired | Harlequin Ichthyosis | HELLP Syndrome | Trichorhinophalangeal Syndrome | Adenosine Deaminase Deficiency | Polycystic Kidney, Autosomal Dominant | Otosclerosis | Subacute Sclerosing Panencephalitis | Amyotrophic Lateral Sclerosis, Juvenile | Glycogen Storage Disease Type 9 | Primary Cutaneous Amyloidosis | Scleroderma, Diffuse | Hereditary Coproporphyria | Mandibuloacral Dysplasia With Type A Lipodystrophy | Pathological Gambling | Glaucomatocyclitic Crisis | Peutz-Jeghers Syndrome | Seasonal Mood Disorder | Cancer, Colon | Congenital Myopathy | Vitreoretinopathy, Proliferative | Asthma | Salla Disease | Pityriasis Rubra Pilaris | Sarcoma, Ewing | Necrotizing Autoimmune Myopathy | B-cell Prolymphocytic Leukemia | Charcot-Marie-Tooth Disease Type 2D | Leukoencephalopathy, Progressive Multifocal | Retinitis Pigmentosa 3 | Cutaneous Angiosarcoma | Congenital Stromal Corneal Dystrophy | Chondroma | Swine Influenza | Pseudomyxoma Peritonei | Raine Syndrome | Cutaneous Lupus Erythematosus | Megaloblastic Anemia | Gastroenteritis | Benign Familial Pemphigus | Spinal Cord Diseases | Esophageal Carcinoma | Desbuquois Syndrome | Keratitis | Asphyxia Neonatorum | Tetanus | Androgenic Alopecia | Nephronophthisis | Evans Syndrome | Peripheral T-cell Lymphoma | Isobutyryl-CoA Dehydrogenase Deficiency | Microcephalic Osteodysplastic Primordial Dwarfism, Type II | Intermittent Claudication | 5-oxoprolinase Deficiency | Oculodentodigital Dysplasia | Vitreoretinal Degeneration, Snowflake Type | Mohr-Tranebjaerg Syndrome | Papilledema | Acrodermatitis | Majeed Syndrome | Filariasis | Cystinosis | Osteoporosis, Postmenopausal | Cirrhosis | Moyamoya Disease | Psoriasis | Neuromuscular Disorders | Spinocerebellar Ataxia Type 28 | Lassa Fever | Camptocormia | Retinoblastoma | Lattice Corneal Dystrophy Type 1 | Epithelial-myoepithelial Carcinoma | Thyrotoxic Periodic Paralysis