Disease

Pfeiffer Syndrome

About the Disease
Pfeiffer Syndrome, also known as infectious mononucleosis, is related to lymphoproliferative syndrome, x-linked, 1 and human cytomegalovirus infection, and has symptoms including fever and pruritus. An important gene associated with Pfeiffer Syndrome is FGFR2 (Fibroblast Growth Factor Receptor 2), and among its related pathways/superpathways are Innate Immune System and ERK Signaling. The drugs Valaciclovir and Anti-Infective Agents have been mentioned in the context of this disorder. Affiliated tissues include skull, bone and spleen, and related phenotypes are ptosis and high palate

Common Targets
FGFR2 | FGFR1

疾病靶点研报
Pfeiffer Syndrome

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

Other Diseases

Macrophagic Myofasciitis | Nicotine Dependence | Wolman Disease | Goiter, Nodular | KBG Syndrome | Encephalopathy, Glycine | Limb Girdle Muscular Dystrophy | Glycogen Storage Disease Type 9 | Congenital Fiber-type Disproportion Myopathy | Dentinogenesis Imperfecta | Blepharoconjunctivitis | Hepatitis D | Pontocerebellar Hypoplasia Type 7 | Cleidocranial Dysplasia | Pneumothorax | Hyperlipidemia | Endophthalmitis | Papilloma | Carney-Stratakis Syndrome | Thrombocytopenia | Cold-induced Sweating Syndrome | Medulloblastoma | Spinocerebellar Ataxia Type 7 | Tietze Syndrome | Thromboembolism | Peripheral Neuropathy | Hashimoto Thyroiditis | Trichorhinophalangeal Syndrome | Hoyeraal-Hreidarsson Syndrome | Cancer, Bladder | Osteopetrosis | Pyruvate Kinase Deficiency | Ghosal Syndrome | Ameloblastoma | Keratosis, Seborrheic | Cholecystitis | Angina Pectoris | Hypolipoproteinemia | Porokeratosis | Anti-glomerular Basement Membrane Disease | Progressive Familial Intrahepatic Cholestasis Type 1 | Charcot-Marie-Tooth Disease, Type 2C | Multiple Sulfatase Deficiency | Klippel-Feil Syndrome | Microvillus Inclusion Disease | Netherton Syndrome | Paroxysmal Nocturnal Hemoglobinuria | Biotinidase Deficiency | Congenital Absence Of Vas Deferens | Bullous Pemphigoid | Perry Syndrome | Scleroderma, Diffuse | Hyperlipidemia Type V | Metabolic Syndrome | Stroke | Pitt-Hopkins Syndrome | Nephroblastoma | Veno-occlusive Disease | Avellino Corneal Dystrophy | Hyperinsulinism-hyperammonemia Syndrome | Leber Hereditary Optic Neuropathy | Diabetes Type 1 | Angioedema, Acquired | Vitamin B12 Deficiency | Acrodysostosis | Spinocerebellar Ataxia Type 13 | Early Infantile Epileptic Encephalopathy 1 | Nance-Horan Syndrome | Periodic Limb Movement Disorder | Woodhouse-Sakati Syndrome | DRESS Syndrome | Trachoma | Vitreoretinopathy, Proliferative | Glycogen Storage Disease Type 0 | Pathological Gambling | 17-beta-hydroxysteroid Dehydrogenase X Deficiency | Williams Syndrome | Charcot-Marie-Tooth Disease, Type 2A | Burn-McKeown Syndrome | Carcinoid Tumor | Myelofibrosis | Intracranial Hypertension | Ulcerative Colitis | Multiple Congenital Anomalies-hypotonia-seizures Syndrome 2 | Fraser Syndrome | Diffuse Idiopathic Pulmonary Neuroendocrine Cell Hyperplasia | Myopathy | Syncope | Pierre Robin Syndrome | Stevens-Johnson Syndrome | Arthritis | Liver Failure, Acute Infantile | Greig Cephalopolysyndactyly Syndrome | Alopecia Totalis | Osmotic Demyelination Syndrome | Familial Pheochromocytoma-paraganglioma | Birk-Barel Syndrome | Autonomic Nervous System Disorders | Diabetic Encephalopathy | Succinic Semialdehyde Dehydrogenase Deficiency | Stuttering | Craniofacial Dysostosis | Kabuki Syndrome | Congenital Bilateral Absence Of Vas Deferens | Hemorrhagic Disorders | Hepatitis, Autoimmune | Sarcosinemia | Myofibrillar Myopathy | Megalencephaly | High Molecular Weight Kininogen Deficiency | Hairy Cell Leukemia | Barrett Esophagus | Norrie Disease | 3-methylcrotonyl-CoA Carboxylase Deficiency | Hemangioma | Leukodystrophies | Macular Corneal Dystrophy Type 1 | X-linked Acrogigantism | Constipation | Temtamy Preaxial Brachydactyly Syndrome | Diabetic Nephropathy | Hepatic Veno-occlusive Disease | Charcot-Marie-Tooth Disease, Type 2 | Diabetic Macular Edema | Birt-Hogg-Dube Syndrome | Hypertension, Renovascular | Pelvic Inflammatory Disease | Familial Advanced Sleep Phase Syndrome | Polyomavirus Nephropathy | Thyrotoxic Periodic Paralysis | Lennox-Gastaut Syndrome | Hypophosphatemic Rickets With Hypercalciuria, Hereditary | Creatine Deficiency Syndrome Due To AGAT Deficiency | Chronic Granulomatous Disease | Cholangiocarcinoma | Cohen Syndrome | Subcortical Band Heterotopia | 5-oxoprolinase Deficiency | Bartter Syndrome | Leukocyte Adhesion Deficiency Type 1 | Gastrointestinal Disorders | Primary Hyperoxaluria Type 1 | Schizophrenia | Generalized Epilepsy And Paroxysmal Dyskinesia | Very Long-chain Acyl-CoA Dehydrogenase Deficiency | Optic Atrophy 2 | Premature Ejaculation | Pyoderma Gangrenosum | Preaxial Polydactyly | Rhabdoid Tumor | Alpers Syndrome | Eating Disorder | Retinitis | Sleep Apnea, Central | Myelitis, Transverse | Mood Disorder | Hypogammaglobulinemia | Shwachman-Bodian-Diamond Syndrome | Microcephaly, Seizures, And Developmental Delay | Peritonitis | Hyperhomocysteinemia | Nephrotic Syndrome Type 1 | Antisocial Personality Disorder | Bronchitis, Chronic | Neuroleptic Malignant Syndrome | Cholestasis, Intrahepatic | Absence Epilepsy | Charcot-Marie-Tooth Disease | Synovitis | Isovaleric Acidemia | Stroke, Ischemic | Swine Influenza | Cerebellofaciodental Syndrome | Liebenberg Syndrome | Precocious Puberty | Pouchitis | Osteoporosis | Exostoses | Ventricular Septal Defect | Meningococcal Meningitis | Congenital Tufting Enteropathy | Diabetes Mellitus, Transient Neonatal | Spinocerebellar Ataxia Type 21 | Leri Pleonosteosis | Greenberg Dysplasia | Endometritis | Osteogenesis Imperfecta Type II | Vestibular Disease | Cryoglobulinemia | Usher Syndrome Type III | Infectious Diarrhea | Cartilage Disorders | Delayed Sleep Phase Syndrome | Spitzoid Melanoma | Acromegaly | Schuurs-Hoeijmakers Syndrome | Mitochondrial Myopathy | Diabetes Type 2 | Martsolf Syndrome | Milk Allergy | Allergic Contact Dermatitis | Mevalonate Kinase Deficiency | Paternal Uniparental Disomy Of Chromosome 14 | Stomatitis | Primary Hyperoxaluria Type 3 | Tuberculous Meningitis | Placenta Previa | Erythema Nodosum | Carpenter Syndrome | Meningococcal Infections | Impulse Control Disorder | Optic Nerve Diseases | Enhanced S-cone Syndrome | Senior-Loken Syndrome | Hydronephrosis | Familial Cerebral Amyloid Angiopathy | Platelet Disorders | Progressive Osseous Heteroplasia | Cardiomyopathy, Hypertrophic | SAPHO Syndrome | Traboulsi Syndrome | Hamartoma | Strabismus | Early Infantile Epileptic Encephalopathy 28 | Frank-ter Haar Syndrome | Presbycusis | Leiomyoma | Mitochondrial DNA Depletion Syndrome, Encephalomyopathic Form | Membranous Nephropathy | Hemochromatosis Type 1 | Crimean-Congo Hemorrhagic Fever | Spinocerebellar Ataxia | Acute Chest Syndrome | Pyelonephritis | Nicotine Addiction | Cysticercosis | Hyperparathyroidism | Amyloidosis | Dysthymia | Pernicious Anemia | Congenital Generalized Lipodystrophy | Heart Failure | Cutis Laxa | X-linked Charcot-Marie-Tooth Disease | Aarskog-Scott Syndrome | Idiopathic Pulmonary Fibrosis | Spinocerebellar Ataxia Type 23 | Bainbridge-Ropers Syndrome | Metatropic Dysplasia | Hypopigmentation | Hypertensive Retinopathy | Multiple Sclerosis, Primary Progressive | Blood Protein Disorders | Urea Cycle Disorder | Moyamoya Disease | Wiskott-Aldrich Syndrome | Osteoporosis, Postmenopausal | Lymphoma Lymphoblastic | Waardenburg Syndrome | Filariasis | Rosacea | Coronary Restenosis | Lymphoma, B-cell | Progressive Encephalopathy-optic Atrophy Syndrome | Glaucomatocyclitic Crisis | Lamellar Ichthyosis | Arterial Tortuosity Syndrome | Hemorrhage | Meningeal Melanocytoma | Glycogen Storage Disease | Overactive Bladder | Gyrate Atrophy Of The Choroid And Retina | Molybdenum Cofactor Deficiency | Congenital Hereditary Endothelial Dystrophy Type I | Insulinoma | Dengue Shock Syndrome | Hemochromatosis Type 2 | Fanconi Anemia | Obesity | Retinal Coloboma | Sweet Syndrome | Craniosynostosis | Kleine-Levin Syndrome | Epicondylitis | Saethre-Chotzen Syndrome | Dermatitis | Cantu Syndrome | Angioedema, Hereditary | Non-Hodgkin Lymphoma | Cholera | 3-methylglutaconic Aciduria Type I | LMNA-related Congenital Muscular Dystrophy | Muir-Torre Syndrome | Polycystic Kidney, Autosomal Dominant | Ataxia-hypogonadism-choroidal Dystrophy Syndrome | Congenital Primary Aphakia | Systemic Lupus Erythematosus | Chromosome 9q34.3 Deletion Syndrome | Dowling-Degos Disease | Asphyxia Neonatorum | Mucolipidosis Type IV | Corneal Dystrophy | Gerodermia Osteodysplastica | Corneal Edema | Irritable Bowel Syndrome | Epidermolysis Bullosa Dystrophica | Agammaglobulinemia | Hyperparathyroidism, Primary | VEXAS Syndrome | Congenital Dyserythropoietic Anemia Type 1 | Astrocytoma | Genee-Wiedemann Syndrome | Encephalopathy | Hepatitis | Chronic Beryllium Disease | Osteonecrosis Of The Jaw | Photosensitivity | Dystonia | Polycythemia Vera | Hyperkalemic Periodic Paralysis | Sezary Syndrome | Periodontitis | Encephalitis | Sleep Apnea | Polyradiculopathy | Presbyopia | 3-methylglutaconic Aciduria Type IV | Colitis | Splenomegaly | Schwannoma | Insulin Resistance | Tremor | Thymoma, Malignant | Warsaw Breakage Syndrome | Fabry's Disease | Epidermolysis Bullosa | Pituitary Dwarfism | Pupil Disorders | Acanthosis Nigricans | Bicuspid Aortic Valve | Glioblastoma | Pneumonia, Viral | Gnathodiaphyseal Dysplasia | Split Hand-foot Malformation | Benign Familial Pemphigus | Diamond-Blackfan Anemia | Heterotopic Ossification | Gynecomastia | Citrullinemia | Glaucoma, Congenital | Primary Biliary Cholangitis | Bernard-Soulier Syndrome | Panuveitis | Proopiomelanocortin Deficiency | Wolfram Syndrome 2 | Infantile Spasm | Megacystis-microcolon-intestinal Hypoperistalsis Syndrome | Hydrolethalus Syndrome | Tinea | Porphyria Cutanea Tarda | Brachydactyly | Sjogren Syndrome | Arthritis, Psoriatic | Bone Giant Cell Tumor | Antenatal Bartter Syndrome Type 1 | Rubinstein-Taybi Syndrome | Oligospermia | X-linked Sideroblastic Anemia | Leprosy | Urticaria | Cardiomyopathy, Dilated, 1L | Amyotrophic Lateral Sclerosis, Juvenile | Fibrosarcoma | Varicocele | Gaucher Disease | Colitis, Microscopic | Neutrophilia | Diabetes Insipidus, Nephrogenic | Myhre Syndrome | Epilepsy, Generalized | Prolidase Deficiency | Riboflavin Transporter Deficiency Neuronopathy | Episodic Ataxia Type 1 | Autoimmune Disease | Myelitis | Triple A Syndrome | Amyotrophic Lateral Sclerosis-parkinsonism-dementia Complex | Sarcoidosis, Pulmonary | Partington Syndrome | Xeroderma Pigmentosum | C3 Glomerulopathy | Polyarteritis Nodosa | Poretti-Boltshauser Syndrome | Dyslexia | Proteus Syndrome | Spinal And Bulbar Muscular Atrophy | Leukocyte Adhesion Deficiency | Colitis, Lymphocytic | CHOPS Syndrome | Tetraplegia