Immunoproliferative Disorders

About the Disease
Hypersensitivity Reaction Type Iv Disease, also known as immunoproliferative disorders, is related to cryoglobulinemia and autoimmune lymphoproliferative syndrome. An important gene associated with Hypersensitivity Reaction Type Iv Disease is CCR6 (C-C Motif Chemokine Receptor 6), and among its related pathways/superpathways are Innate Immune System and Cytokine Signaling in Immune system. The drugs D-Tyrosine and Antibodies have been mentioned in the context of this disorder. Affiliated tissues include t cells, small intestine and bone marrow, and related phenotypes are endocrine/exocrine gland and neoplasm

Common Targets
ADORA2B | ADORA2A | HCK

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

Other Diseases

Lattice Corneal Dystrophy | Retinopathy Of Prematurity | Primary Erythromelalgia | Arteriovenous Malformations | Acute Tubular Necrosis | Asthma, Nocturnal | Mosaic Variegated Aneuploidy Syndrome 2 | Hemoglobinopathies | Optic Nerve Diseases | Myosin Storage Myopathy | Vogt-Koyanagi-Harada Syndrome | Chitayat Syndrome | Carney-Stratakis Syndrome | Retinoblastoma | Hyperinsulinism-hyperammonemia Syndrome | Encephalocele | Zygomycosis | Oligospermia | Hyperammonemia | Hypertension | Tardive Dyskinesia | Acromegaly | Optic Nerve Hypoplasia, Bilateral | Delirium | Acute Leukemia | Osteoporosis-pseudoglioma Syndrome | SAPHO Syndrome | Crisponi Syndrome | Enterocolitis, Necrotizing | Glomerulonephritis, Membranous | Glomerulonephritis, Membranoproliferative | Meckel-Gruber Syndrome | Hereditary Spastic Paraplegia | Waardenburg Syndrome Type 4 | Bardet-Biedl Syndrome | Migraine | Lennox-Gastaut Syndrome | Fibronectin Glomerulopathy | Aphasia | Glutaric Aciduria Type 2 | Pyruvate Carboxylase Deficiency Disease | Hydrocephalus | Chondrodysplasia Punctata | Thrombasthenia | Charcot-Marie-Tooth Disease Type 4B1 | Chromosome 5q Deletion Syndrome | Paget's Disease Of The Breast | Apert Syndrome | Neuromyelitis Optica | Zellweger Syndrome | Hypotension, Orthostatic | Polymicrogyria | Donnai-Barrow Syndrome | Sickle Cell Disease | Congenital Adrenal Hyperplasia | Rhabdomyosarcoma, Embryonal | Paraplegia | Esophagitis | Heavy Chain Disease | Bone Giant Cell Tumor | Reflex Epilepsy | Bethlem Myopathy | Arthropathy | Episodic Ataxia Type 2 | Restrictive Dermopathy | Okihiro Syndrome | Poretti-Boltshauser Syndrome | Angina Pectoris | Myositis, Focal | Tracheal Disorders | Keratosis, Actinic | Hereditary Sensory Neuropathy Type 1 | Coffin-Siris Syndrome | Cancer, Breast | VACTERL/VATER Association | Hyperparathyroidism, Primary | Smith-Lemli-Opitz Syndrome | Sarcoidosis, Pulmonary | Colitis | Atrioventricular Septal Defect | Dyskeratosis Congenita | Mumps | Chorea-acanthocytosis | Learning Disability | Cornelia De Lange Syndrome | Postaxial Polydactyly | Opisthorchiasis | Hyperinsulinemia | Waardenburg Syndrome Type 1 | Oral Lichen Planus | Leishmaniasis, Cutaneous | NGLY1 Deficiency | Arteriosclerosis | Multiple Congenital Anomalies-hypotonia-seizures Syndrome 2 | Heroin Dependence | Gout | Anodontia | Achromatopsia | Sickle Cell Anemia | Pyruvate Dehydrogenase Deficiency | Myeloid Leukemia | Autoimmune Polyendocrinopathy Syndrome Type I | Hypopigmentation | Perivascular Epithelioid Cell Tumor | Gastroenteritis | Riboflavin Transporter Deficiency Neuronopathy | Adenylosuccinate Lyase Deficiency | Thyroid Dysgenesis | Glutathione Synthetase Deficiency | Myoclonic Epilepsy With Ragged Red Fibers | Acute Generalized Exanthematous Pustulosis | Galactosialidosis | Long QT Syndrome Type 2 | Giant Axonal Neuropathy | Platelet Disorders | Androgenic Alopecia | Microcephaly, Seizures, And Developmental Delay | Keratoconjunctivitis | Hemolytic Anemia | Dysplastic Nevus | Cancer, Brain | Orotic Aciduria | Nephrosclerosis | Pneumonia, Bacterial | Antenatal Bartter Syndrome Type 1 | Tietze Syndrome | Erectile Dysfunction | Thyrotoxic Periodic Paralysis | Celiac Disease | Spinocerebellar Ataxia Type 20 | Nicotine Dependence | Encephalopathy, Hepatic | Leiomyoma | Pompe Disease | Sarcomatoid Carcinoma Of The Lung | Basal Ganglia Disease | Schaaf-Yang Syndrome | Basal Ganglia Disease, Biotin-responsive | Arthritis, Psoriatic | Primary Sclerosing Cholangitis | Hypercalcemia | Analgesia | Posterior Polar Cataract | Cocaine-Related Disorders | Greenberg Dysplasia | Autoimmune Disease | Persistent Hyperplastic Primary Vitreous | Ellis-Van Creveld Syndrome | Superficial Spreading Melanoma | Spondylo-ocular Syndrome | Osteoarthritis | Ependymoma | Gangliosidosis, GM1 | Low Tension Glaucoma | Bronchitis, Chronic | Osteosarcoma | Creatine Deficiency Syndrome | Thymoma, Malignant | Paternal Uniparental Disomy Of Chromosome 14 | Nephroblastoma | Parkinson Disease 6, Autosomal Recessive Early-onset | Hypercholesterolemia | Cellulitis | Polycythemia Vera | Carcinoma, Squamous Cell | Primary Progressive Nonfluent Aphasia | Angioedema, Acquired | Primrose Syndrome | Protein S Deficiency | Anovulation | Axenfeld-Rieger Syndrome | Asplenia | Papillorenal Syndrome | Benign Hereditary Chorea | Hypogammaglobulinemia | Hemorrhage | Cone Dystrophy | Optic Neuritis | Johanson-Blizzard Syndrome | Hepatorenal Syndrome | Myotonic Disorders | Prune Belly Syndrome | Mastitis | Fukuyama Congenital Muscular Dystrophy | Adrenoleukodystrophy, X-linked | Diffuse Palmoplantar Keratoderma | Cri-du-chat Syndrome | Spinocerebellar Ataxia Type 8 | Aneurysm, Thoracic Aortic | Precocious Puberty | Ulcerative Colitis | Vitelliform Macular Dystrophy | Prediabetes | Stargardt Disease | Oligoastrocytoma | Hoyeraal-Hreidarsson Syndrome | Gastroschisis | Glycogen Storage Disease Type 0, Muscle | Wolman Disease | Homocystinuria | Cirrhosis | Transient Bullous Dermolysis Of The Newborn | CHARGE Syndrome | Spinocerebellar Ataxia Type 2 | Spinocerebellar Ataxia Type 27 | Tendinitis | Asphyxia Neonatorum | Rolandic Epilepsy | Otitis Externa | Ectodermal Dysplasia | Blepharophimosis Syndrome | T-cell Chronic Lymphocytic Leukemia | Occipital Neuralgia | Eccrine Porocarcinoma | Noonan Syndrome-like Disorder With Loose Anagen Hair | Focal Segmental Glomerulosclerosis | Marfan Syndrome | Schistosomiasis Mansoni | Pineoblastoma | Spinocerebellar Ataxia | Centronuclear Myopathy | Urofacial Syndrome | Tonsillitis | Persistent Mullerian Duct Syndrome | Primary Familial Brain Calcification | Spinal Muscular Atrophy | Low Phospholipid Associated Cholelithiasis | Neurodegeneration Due To Cerebral Folate Transport Deficiency | Addison Disease | Astrocytoma | Epilepsy Of Infancy With Migrating Focal Seizures | Hashimoto Thyroiditis | Multicystic Renal Dysplasia | Molybdenum Cofactor Deficiency | Cholelithiasis | Pain | Keloid | Glutaric Aciduria Type 3 | Hypoproteinemia, Hypercatabolic | X-linked Acrogigantism | Porphyria | Schizophrenia | Proximal Symphalangism | Osteochondrosis | T-cell Leukemia | Osteogenesis Imperfecta Type IV | Hyperparathyroidism-jaw Tumor Syndrome | X-linked Myotubular Myopathy | Pemphigus | Very Long-chain Acyl-CoA Dehydrogenase Deficiency | Rubinstein-Taybi Syndrome | Paracoccidioidomycosis | Polydactyly | Corneal Dystrophies, Hereditary | Arrhythmogenic Right Ventricular Cardiomyopathy | Synovitis | Smoldering Myeloma | Rash | Pathological Gambling | Osteochondroma | Pleural Tuberculosis | Fraser Syndrome | Pregnancy, Ectopic | Spastic Paraplegia Type 7 | DEND Syndrome | Congenital Adrenal Hyperplasia 1 | Ocular Surface Squamous Neoplasia | Metabolic Diseases | Endometriosis | Basal Cell Nevus Syndrome | Anuria | Neonatal Progeroid Syndrome | Cystitis | Goldenhar Syndrome | Chromosome 8q21.11 Deletion Syndrome | Acromicric Dysplasia | Demyelinating Diseases | Parkinson's Disease | Hepatitis B, Chronic | Methylmalonic Aciduria And Homocystinuria, CblC Type | Pituitary Disorders | Brachial Plexus Neuropathy | Cramp Fasciculation Syndrome | Pyloric Stenosis, Infantile Hypertrophic | HELLP Syndrome | Erythema Multiforme | Intestinal Tuberculosis | Neurofibromatosis | Intermittent Explosive Disorder | Gitelman Syndrome | Esophagitis, Eosinophilic | Hypoplastic Left Heart Syndrome | Facioscapulohumeral Muscular Dystrophy | Oculocutaneous Albinism | Blood Protein Disorders | Paraganglioma, Carotid Body | Pontocerebellar Hypoplasia Type 2 | Oguchi Disease-2 | MELAS Syndrome | Early Infantile Epileptic Encephalopathy | Hereditary Mixed Polyposis Syndrome | Hemangioma | Von Willebrand Disease | Primary Biliary Cholangitis | Neurocutaneous Syndromes | Pseudo-pseudohypoparathyroidism | FG Syndrome | Skin Papilloma | Blomstrand Osteochondrodysplasia | Thyroid Hormone Resistance | Platyspondylic Lethal Skeletal Dysplasia, Torrance Type | Prolymphocytic Leukemia | Cholesteryl Ester Storage Disease | Keratitis-ichthyosis-deafness Syndrome | Neuropathy | Hyperphenylalaninemia | Fundus Albipunctatus | Keratopathy | Weill-Marchesani Syndrome | Charcot-Marie-Tooth Disease, Type 2 | Combined Deficiency Of Factor V And Factor VIII | Glycogen Storage Disease Type 0 | Basan Syndrome | Psoriasis | Overactive Bladder | Microphthalmia, Syndromic 7 | Facioscapulohumeral Muscular Dystrophy Type 2 | Thrombocytopenia | Otopalatodigital Syndrome Type 2 | Non-epidermolytic Palmoplantar Keratoderma | Meleda Disease | Recurrent Respiratory Papillomatosis | Amyotrophic Lateral Sclerosis | Cancer, Kidney | Split Hand-foot Malformation | Brugada Syndrome 1 | Liddle Syndrome | Isovaleric Acidemia | Hepatitis C, Chronic | Glaucoma | Maple Syrup Urine Disease | Mevalonate Kinase Deficiency | Christianson Syndrome | Bullous Pemphigoid | Pheochromocytoma | Spinocerebellar Ataxia Type 5 | Congenital Stationary Night Blindness | Spitzoid Melanoma | Wiedemann-Steiner Syndrome | Sclerosteosis | Generalized Epilepsy And Paroxysmal Dyskinesia | 3-hydroxyacyl-CoA Dehydrogenase Deficiency | Kaposiform Hemangioendothelioma | Roberts Syndrome | X-linked Sideroblastic Anemia | Marshall-Smith Syndrome | Pyruvate Decarboxylase Deficiency | Spondylocostal Dysostosis | Diabetic Macular Edema | Hyperbilirubinemia | Oculocutaneous Albinism Type 4 | Ocular Albinism Type 1 | Distal Myopathy | Spinal Muscular Atrophy With Progressive Myoclonic Epilepsy | Autism Spectrum Disorders | Cranial Nerve Disease | Adams-Oliver Syndrome | Thyroiditis | Seborrheic Dermatitis | Choroiditis | AIDS Dementia Complex | Connective Tissue Disorders | Hyperparathyroidism, Secondary | Multifocal Motor Neuropathy | Hyperuricemic Nephropathy, Familial Juvenile | 6-pyruvoyl-tetrahydropterin Synthase Deficiency | Multiple System Atrophy | Chronic Mucocutaneous Candidiasis | Brachydactyly | Adenoma, Villous | Hereditary Sensory And Autonomic Neuropathy | Peutz-Jeghers Syndrome | Hypophosphatemic Rickets, Autosomal Recessive, 1 | Neuronal Ceroid Lipofuscinosis | Sleep Apnea, Central | Retinoschisis | Pleomorphic Xanthoastrocytoma | Preaxial Polydactyly | Stevens-Johnson Syndrome | Coenzyme Q10 Deficiency | Hereditary Multiple Exostoses | Osteonecrosis Of The Jaw | Anencephaly | Mitochondrial DNA Depletion Syndrome, Hepatocerebral Form | Vaginitis | Crimean-Congo Hemorrhagic Fever | Arthritis, Gouty | PASLI Disease | Premenstrual Syndrome | Prader-Willi Syndrome