Disease

Eosinophilia

About the Disease
Hypereosinophilic Syndrome, also known as eosinophilia, is related to hypereosinophilic syndrome, idiopathic and primary hypereosinophilic syndrome, and has symptoms including pruritus, myalgia and abdominal pain. An important gene associated with Hypereosinophilic Syndrome is FIP1L1 (Factor Interacting With PAPOLA And CPSF1), and among its related pathways/superpathways are Innate Immune System and Signal Transduction. The drugs Prednisone and Benzocaine have been mentioned in the context of this disorder. Affiliated tissues include bone marrow, heart and bone, and related phenotypes are Decreased viability and Decreased viability

Common Targets
SCGB1A1 | IL3 | LIN7A | SIRPA | TMEM273 | JAK2 | G7157 | RIN3 | RPTN | APP | IL13 | VTN | ACOT7 | RASSF2 | LPIN1 | CEBPE

疾病靶点研报
Eosinophilia

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

Other Diseases

Disseminated Superficial Actinic Porokeratosis | Hepatitis, Chronic | Hyperostosis | Pemphigoid | Gingivitis | Turner's Syndrome | Primary Progressive Aphasia | Polycystic Ovary Syndrome | Hyperhomocysteinemia | Canavan Disease | Graft-versus-host Disease | Actinomycetoma | Peeling Skin Syndrome Type B | Unverricht-Lundborg Syndrome | Spinocerebellar Ataxia Type 1 | Sarcoma, Alveolar Soft Part | Neurodegeneration With Brain Iron Accumulation | Hypertension, Pulmonary | Barakat Syndrome | Glycogen Storage Disease Type 1 | Apparent Mineralocorticoid Excess Syndrome | Zimmermann-Laband Syndrome | Glutathione Synthetase Deficiency | Spondyloarthritis | Renal Tubular Acidosis | Sarcosinemia | B-cell Prolymphocytic Leukemia | Protein S Deficiency | Giant Cell Glioblastoma | Sarcoma | Conjunctivitis | Hyperthermia, Malignant | Acute Lymphocytic Leukemia | Pure Red Cell Aplasia | Familial Advanced Sleep Phase Syndrome | IgA Nephropathy | Pituitary Stalk Interruption Syndrome | Sponastrime Dysplasia | Dementia | Hypophosphatasia | Encephalopathy, Ethylmalonic | Connective Tissue Disorders | Cri-du-chat Syndrome | Benign Familial Infantile Seizures | Senior-Loken Syndrome | Uremic Pruritus | Dementia, Vascular | Gallstones | Multicystic Renal Dysplasia | Nutrition Disorders | Chordoma | Gynecomastia | Citrullinemia | Paraganglioma, Carotid Body | 3-methylcrotonyl-CoA Carboxylase Deficiency | Keratoconus | Adenoma, Pituitary | Hepatic Steatosis | Congenital Ichthyosiform Erythroderma | T-cell Lymphoma, Subcutaneous Panniculitis-like | Basal Ganglia Cerebrovascular Disease | Beta-Propeller Protein-associated Neurodegeneration | Leigh Syndrome | Cancer, Breast | Multiple Sclerosis, Primary Progressive | Pseudohypoparathyroidism Type 1A | Cancer, Skin | Tatton-Brown-Rahman Syndrome | Melanocytic Nevus | C3 Glomerulonephritis | Spinocerebellar Ataxia Type 21 | Rhabdoid Tumor | Familial Partial Lipodystrophy | Periventricular Leukomalacia | Basal Ganglia Disease | Down Syndrome | Open-angle Glaucoma | Gastritis | Iron Overload | Myasthenia Gravis | Anorexia Nervosa | Nicolaides-Baraitser Syndrome | Blue Nevus | B-cell Chronic Lymphocytic Leukemia | Lichen Sclerosus | Duodenal Atresia | Polymicrogyria | Lymphangiomatosis | Hypertelorism | Walker-Warburg Syndrome | Immunoproliferative Disorders | Behavioral Variant Of Frontotemporal Dementia | Schizophrenia | Leri Pleonosteosis | Opisthorchiasis | Myoclonic Atonic Epilepsy | Papulopustular Rosacea | Hemolytic Uremic Syndrome, Atypical | Chordoid Glioma | Bleeding Disorder Due To CalDAG-GEFI Deficiency | Inflammatory Joint Disease | Knobloch Syndrome | Progressive Osseous Heteroplasia | Nasodigitoacoustic Syndrome | Acute Generalized Exanthematous Pustulosis | Inborn Errors Of Metabolism | Genee-Wiedemann Syndrome | Microcephalic Osteodysplastic Primordial Dwarfism, Type I | Fibrodysplasia Ossificans Progressiva | Pulmonary Sclerosing Hemangioma | Takotsubo Cardiomyopathy | Hartsfield Syndrome | Lymphoma Lymphoblastic | Strabismus | Lymphoma, Mantle Cell | Syphilis | Charcot-Marie-Tooth Disease | Heroin Dependence | Paget's Disease Of The Breast | Angina Pectoris | Usher Syndrome | Blau Syndrome | Anorectal Malformations | PASLI Disease | Macrophagic Myofasciitis | Anxiety Disorders | Borjeson-Forssman-Lehmann Syndrome | Sitosterolemia | Bulimia Nervosa | Polycythemia | Intestinal Pseudo-obstruction | Allan-Herndon-Dudley Syndrome | Amyotrophic Lateral Sclerosis-parkinsonism-dementia Complex | Bethlem Myopathy | Charcot-Marie-Tooth Disease, Type 2C | Takayasu's Arteritis | Goiter, Nodular | Trachoma | Pyoderma Gangrenosum | Congenital Mirror Movements | Dengue Hemorrhagic Fever | Ichthyosis Bullosa Of Siemens | Arthritis, Gouty | Cholestasis | Prune Belly Syndrome | Vascular Calcification | Keratosis, Seborrheic | Ameloblastic Carcinoma | Congenital Adrenal Hyperplasia 1 | Myelodysplasia | Kallmann Syndrome | Alopecia | Osteochondroma | Meesmann Corneal Dystrophy | Pheochromocytoma | Pancreatitis, Chronic | Hypersomnia | Familial Glucocorticoid Deficiency | Progressive Encephalopathy-optic Atrophy Syndrome | Dyslipidemia | Malaria | Fanconi Syndrome | Spondylocostal Dysostosis | Keratitis-ichthyosis-deafness Syndrome | Vitamin K Deficiency | Insulin Resistance | Angelman Syndrome | Neuroendocrine Cancer | Imerslund-Grasbeck Syndrome | Lymphangioleiomyomatosis | Chondrodysplasia Punctata | Cryoglobulinemia | Deafness, Dystonia, And Cerebral Hypomyelination | Trichuriasis | Dysthymia | Sleep Apnea, Central | Osteoporosis-pseudoglioma Syndrome | Seborrheic Dermatitis | Ocular Surface Squamous Neoplasia | Loeys-Dietz Syndrome | Jawad Syndrome | Endometriosis | Loeys-Dietz Syndrome Type 4 | Familial Mediterranean Fever | Mandibuloacral Dysplasia With Type A Lipodystrophy | Carney Triad | 3-hydroxy-3-methylglutaryl-CoA Synthase Deficiency | Congenital Absence Of Vas Deferens | Blastomycosis | Fetal And Neonatal Alloimmune Thrombocytopenia | Fibromuscular Dysplasia | Nevus | Proteasome-associated Autoinflammatory Syndrome 2 | Thyroid Dysgenesis | Dyskeratosis Congenita | Tuberculosis | Low Phospholipid Associated Cholelithiasis | Ectodermal Dysplasia | Mitochondrial Myopathy | Dominant Optic Atrophy | Renal-hepatic-pancreatic Dysplasia | Autoimmune Polyendocrinopathy Syndrome Type I | Agnathia-Otocephaly Complex | Lipid Storage Myopathy | Pre-eclampsia | Micropenis | Fascioliasis | Veno-occlusive Disease | Pericarditis | Microcephaly, Seizures, And Developmental Delay | Distal Myopathy | Focal Dermal Hypoplasia | Autoimmune Interstitial Lung, Joint, And Kidney Disease | Galloway-Mowat Syndrome | MELAS Syndrome | Corneal Dystrophy And Perceptive Deafness | Hydrops Fetalis | Wolfram Syndrome 2 | Agoraphobia | Yellow Fever | Mabry Syndrome | Dystonia | Binge Eating Disorder | Schistosomiasis Mansoni | Chronic Inflammatory Demyelinating Polyneuropathy | Urethritis | Multiple Sulfatase Deficiency | Fibrillation, Atrial | Palsy, Cerebral | Polycystic Liver | Anal Fissure | Kabuki Syndrome 2 | Sickle Cell Disease | Spondylo-ocular Syndrome | Varicocele | Addison Disease | Enlarged Vestibular Aqueduct | Pseudohypoparathyroidism Type 1B | Epidermolysis Bullosa Dystrophica | Hepatitis C, Chronic | Cryptococcal Meningitis | Pulmonary Capillary Hemangiomatosis | Pachyonychia Congenita | Chudley-McCullough Syndrome | Pulmonary Alveolar Microlithiasis | Gestational Trophoblastic Disease | Sialoadenitis | Aarskog-Scott Syndrome | Periodontitis | Glycogen Storage Disease Type 0 | Craniofacial Dysostosis | Huntington's Disease | Histiocytosis | Krabbe Disease | Sialidosis Type I | Osteosclerosis | Adenosine Deaminase 2 Deficiency | Inflammatory Bowel Disease | Chronic Idiopathic Myelofibrosis | Exotropia | Headache | Asperger Syndrome | Bainbridge-Ropers Syndrome | Scabies | Exocrine Pancreatic Insufficiency | Osteogenesis Imperfecta Type III | Bardet-Biedl Syndrome | Episodic Ataxia | Congenital Adrenal Hyperplasia | Mosaic Variegated Aneuploidy Syndrome 2 | Ileitis | Lymphoproliferative Disorders | Empyema | Sarcomatoid Carcinoma Of The Lung | Uveitis, Anterior | Papilledema | Keratosis | Hemangioma | Myocarditis | Prediabetes | Myopathy | Schizencephaly | Hernia, Inguinal | Eczema | Desmosterolosis | Neonatal Progeroid Syndrome | Tardive Dyskinesia | Corneal Edema | Acute Leukemia | Primary Ovarian Insufficiency | Danon Disease | Autism Spectrum Disorders | KBG Syndrome | Carey-Fineman-Ziter Syndrome | Blepharospasm | Macrophage Activation Syndrome | Growth Hormone Excess | Hereditary Hemorrhagic Telangiectasia Type 2 | Analgesia | Anorchia | Sleep Apnea, Obstructive | Colitis, Lymphocytic | Glycogen Storage Disease | Prurigo Nodularis | Cranial Nerve Disease | Autosomal Recessive Congenital Ichthyosis | Macular Corneal Dystrophy | Seizures-scoliosis-macrocephaly Syndrome | Sensory Neuropathy | Ichthyosis, X-linked | Pulmonary Stenosis | Progressive Familial Intrahepatic Cholestasis Type 1 | Rhabdomyosarcoma, Alveolar | Spitz Nevus | Celiac Disease | Tetanus | Spondylosis | Gaucher Disease | Toxic Epidermal Necrolysis | Hermansky-Pudlak Syndrome | Histiocytic Sarcoma | Methemoglobinemia Type IV | Costello Syndrome | Meier-Gorlin Syndrome | Learning Disability | Fibrosarcoma | Odonto-onycho-dermal Dysplasia | Diabetic Neuropathy | Congenital Hypofibrinogenemia | Gastroenteritis, Eosinophilic | Kleine-Levin Syndrome | Liddle Syndrome | Chromosome 17q21.31 Deletion Syndrome | Reticular Dysgenesis | Facioscapulohumeral Muscular Dystrophy | Giant Axonal Neuropathy | Spinocerebellar Ataxia Type 7 | Urticaria | Hemophagocytic Lymphohistiocytosis | Muir-Torre Syndrome | Chediak-Higashi Syndrome | Renal Failure | Fontaine Progeroid Syndrome | Central Retinal Artery Occlusion | Meleda Disease | Panuveitis | Aldosteronism | Peters-plus Syndrome | VACTERL Association | Thrombotic Microangiopathy | Scoliosis | Carcinoma, Squamous Cell | Marfan Syndrome | Niemann-Pick Disease, Type C | Nicotine Addiction | Pulmonary Veno-occlusive Disease | Neuromuscular Disorders | Paracoccidioidomycosis | Crouzon Syndrome With Acanthosis Nigricans | Diabetes Type 2 | Cleidocranial Dysplasia | Axenfeld-Rieger Syndrome | Cholelithiasis | Lymphoma, Follicular | CHOPS Syndrome | Camurati-Engelmann Disease | 3-methylglutaconic Aciduria Type I | Asphyxia Neonatorum | Impulse Control Disorder | Gastroschisis | Pneumonia, Viral | Nephronophthisis | Muscle Wasting | Pontocerebellar Hypoplasia Type 2 | Ganglioglioma | Craniometaphyseal Dysplasia | Epidermolysis Bullosa | Placenta Previa | Carotid Artery Disease | Olmsted Syndrome | Pontocerebellar Hypoplasia Type 7 | Epidermolysis Bullosa Simplex, Dowling-Meara Type | Congenital Muscular Dystrophy | Idiopathic Multicentric Castleman Disease | Prader-Willi Syndrome | Fragile X Syndrome | Hypoproteinemia, Hypercatabolic | Crohn's Disease | Arthritis, Psoriatic | Adenomatoid Tumor | Glomerulonephritis, Membranous | Cornelia De Lange Syndrome | Multiple System Atrophy | GATA2 Deficiency | Hypoparathyroidism | Schizotypal Personality Disorder | Pneumococcal Meningitis | Goldenhar Syndrome | Noonan Syndrome-like Disorder With Loose Anagen Hair | Trichothiodystrophy