Rhinitis
Rhinitis
About the Disease
Chronic Rhinitis, also known as chronic rhinitis nos, is related to giant papillary conjunctivitis and allergic conjunctivitis, and has symptoms including purulent rhinitis, rhinorrhea and catarrh. An important gene associated with Chronic Rhinitis is HRH1 (Histamine Receptor H1), and among its related pathways/superpathways are Hematopoietic Stem Cells and Lineage-specific Markers and Allograft rejection. The drugs Dexlansoprazole and Lansoprazole have been mentioned in the context of this disorder. Affiliated tissues include eye, skin and bone, and related phenotypes are immune system and respiratory system
Common Targets
DRD2 | TYK2 | ADRA1A | IKBKB | TRPM8 | ORAI1 | ALOX5AP | Tachykinin Receptor (nonspecified subtype) | G1432 | FLG | Alpha-2 Adrenergic receptors (nonspecified subtype) | LPAR1 | ADRA2B | TRPV1 | DHODH | Calcium release-activated channel (CRAC) | NR3C1 | CCR4 | alpha-Adrenoceptor (nonspecified subtype) | MAP3K14 | CLC | ADRA2A | IL10 | CHRM3 | PTGDR | MMP2 | PTGDR2 | CCR8 | GSDMB | IL1A | ABCC8 | G3569 | EPX | MMP13 | HRH1 | Dopamine receptor (nonspecified subtype) | JAK2 | ADRB2 | Muscarinic Acetylcholine Receptor (mAChR) (nonspecified subtype) | alpha1-Adrenoceptor (nonspecified subtype) | JAK3 | NF-kappaB (NFkB) | G3576 | JAK1 | PDE4A | Adrenoceptor (nonspecified subtype) | ALOX5 | MAPK13 | G7124 | HRH4 | PDE4D | ADRA2C | HRH3 | Phosphodiesterase IV (PDE4) (nonspecified subtype) | CCR3 | ELANE
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Other Diseases
Tetraplegia | Barrett Esophagus | Ocular Hypertension | Mumps | Adenoma, Villous | Fibronectin Glomerulopathy | Hereditary Mixed Polyposis Syndrome | Multiple Epiphyseal Dysplasia | Aicardi-Goutieres Syndrome | Warsaw Breakage Syndrome | Hemangioma | Ganglioglioma | Mucolipidosis | Meningioma | Hypertension, Renovascular | Sclerosteosis 2 | Enlarged Vestibular Aqueduct | Nephropathy | Craniometaphyseal Dysplasia | Spinal Muscular Atrophy | Charcot-Marie-Tooth Disease Type 4 | Double Outlet Right Ventricle | Miyoshi Myopathy | Renal Tubular Acidosis | Dubin-Johnson Syndrome | Inborn Errors Of Metabolism | Myelodysplasia | Glycogen Storage Disease Type 4 | Esthesioneuroblastoma | Metaphyseal Chondrodysplasia, Schmid Type | Wolfram Syndrome 2 | Usher Syndrome Type III | Vitreoretinal Degeneration, Snowflake Type | Ichthyosis | Nutrition Disorders | Fontaine Progeroid Syndrome | Takenouchi-Kosaki Syndrome | Anemia | Hypothalamic Obesity | Muscle Wasting | Keratopathy | Chronic 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Essential Fructosuria | Spinocerebellar Ataxia Type 6 | Dengue Shock Syndrome | Lymphopenia | Early Infantile Epileptic Encephalopathy 1 | Riboflavin Transporter Deficiency Neuronopathy | Cold-induced Sweating Syndrome | Carcinoid Syndrome | Primary Familial Brain Calcification | Greig Cephalopolysyndactyly Syndrome | Diabetes Type 1 | Benign Recurrent Intrahepatic Cholestasis 1 | Cleidocranial Dysplasia | Renal Hypouricemia | Sjogren Syndrome | Nicotine Dependence | Sarcoma, Ewing | Hepatitis B, Chronic | Cancer, Kidney | Hemoglobinopathies | Primary Progressive Aphasia | Acne Vulgaris | Hepatopulmonary Syndrome | Spinocerebellar Ataxia Type 1 | Stevens-Johnson Syndrome | Spinocerebellar Ataxia Type 8 | Waardenburg Syndrome Type 4A | Ischemia | Keratosis, Actinic | Palsy, Cerebral | Heroin Dependence | Erdheim-Chester Disease | Pigment Dispersion Syndrome | Spinocerebellar Ataxia Type 38 | Neovascular Glaucoma | Wilson's Disease | Acute Coronary Syndrome | Polydactyly | Waardenburg Syndrome Type 2E | Alpha-thalassemia Myelodysplasia Syndrome | Viral Meningitis | Neuroblastoma | Charcot-Marie-Tooth Disease Type 4D | Pain | Microcephalic Primordial Dwarfism | Coffin-Siris Syndrome | Distal Myopathy 2 | Pleural Tuberculosis | Vici Syndrome | Multiple Myeloma | Diabetic Neuropathy | Impetigo | Phosphoglycerate Dehydrogenase Deficiency | Iron Overload | Wolfram Syndrome | Chordoma | Pregnancy, Ectopic | AIDS | Cocaine-Related Disorders | Hypertriglyceridemia | Bone Marrow Necrosis | Polycythemia Vera | Retinoblastoma | Primary Carnitine Deficiency | X-linked Sideroblastic Anemia | Holt-Oram Syndrome | Congenital Nephrotic Syndrome | Sotos Syndrome | Hypermethioninemia | Hyperlipidemia, Familial Combined | Lymphoproliferative Disorders | T-cell Chronic Lymphocytic Leukemia | Lamellar Ichthyosis | Antiphospholipid Syndrome | Methylmalonic Aciduria And Homocystinuria, CblC Type | Pancreatitis, Chronic | Metabolic Syndrome | Porphyria Cutanea Tarda | Dent Disease | 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3-methylglutaconic Aciduria | Retinitis