Stomatitis

About the Disease
Stomatitis is related to viral infectious disease and ebola hemorrhagic fever, and has symptoms including enanthema, oral manifestations and oral pain. An important gene associated with Stomatitis is VDI (Vesicular Stomatitis Virus Defective Interfering Particle Suppression), and among its related pathways/superpathways are Innate Immune System and Cytokine Signaling in Immune system. The drugs Benzocaine and Tannic acid have been mentioned in the context of this disorder. Affiliated tissues include bone marrow, breast and lung, and related phenotype is immune system.

Common Targets
ICAM1 | CASP8 | GSTT1 | CANX | SELL | CDA | GSK3B | Mucin (nonspecified subtype) | VCAM1 | SLC19A1 | GSTP1 | APC | DCX (DDB1-CUL4-X-box) E3 protein ligase complex | UGT1A6 | CTNNB1 | CRBN | ICAM5 | UGT1A1 | Nitric oxide synthase (NOS) (nonspecified subtype) | SLCO1B1 | VCP | Vacuolar H+ ATPase | G6774 | TIGIT | ACE | MTHFR | G5243 | CALCR | DPYD | WNT2 | SELE | NR3C1 | G7124 | XBP1 | HSP90B1 | G9429 | G3309 | HMGCR

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Other Diseases

Optic Neuritis | Colorectal Adenoma | L-2-Hydroxyglutaric Aciduria | Eczema | Corneal Edema | Hypohidrotic Ectodermal Dysplasia | Sleep Disorder | Waardenburg Syndrome | Central Retinal Artery Occlusion | Brooke-Spiegler Syndrome | Schaaf-Yang Syndrome | Pantothenate Kinase-associated Neurodegeneration | Von Willebrand Disease | Hemolytic Anemia | Rheumatic Heart Disease | Neurotoxicity | Charcot-Marie-Tooth Disease, Type 1A | Spinocerebellar Ataxia Type 7 | Hypertension, Renal | Silicosis | Farber Disease | Presbycusis | Epidermolytic Hyperkeratosis | Colitis, Microscopic | Acromicric Dysplasia | Contact Dermatitis | Dupuytren Disease | Rolandic Epilepsy | Gastric Atrophy | Conn Syndrome | Spinocerebellar Ataxia | Retinoblastoma | Retinitis Pigmentosa | Nestor-Guillermo Progeria Syndrome | Keratosis, Actinic | Micro Syndrome | Neurodevelopmental Disorders | Megalencephaly | Charcot-Marie-Tooth Disease Type 2E | Batten Disease | Reflex Epilepsy | Abetalipoproteinemia | Melnick-Needles Syndrome | Porphyria | Acute Lymphocytic Leukemia | DRESS Syndrome | Enterocolitis, Necrotizing | Antenatal Bartter Syndrome Type 1 | Hypervalinemia | Lipoma | Trichorhinophalangeal Syndrome | Hepatoblastoma | Vici Syndrome | Autosomal Recessive Spastic Paraplegia Type 54 | Tinea | Perry Syndrome | Tetraplegia | Histoplasmosis | Alopecia Areata | Liver Diseases | Giant Axonal Neuropathy | Cervical Dystonia | Usher Syndrome Type IIC | Androgenic Alopecia | Viral Meningitis | Progressive Familial Intrahepatic Cholestasis Type 2 | Polycystic Ovary Syndrome | Von Hippel-Lindau Disease | Antithrombin III Deficiency | Narcolepsy | Rhabdomyosarcoma, Embryonal | Neurofibrosarcoma | Creatine Deficiency Syndrome | Primrose Syndrome | Nasodigitoacoustic Syndrome | VEXAS Syndrome | Osteoporosis-pseudoglioma Syndrome | CHARGE Syndrome | Hemochromatosis | Blepharophimosis Syndrome | Nephroblastoma | Acanthosis Nigricans | Vasculitis | Pearson Syndrome | Retinal Dystrophy, Early-onset Severe | Glutaric Aciduria Type 2 | Subcortical Band Heterotopia | Albinism | Paroxysmal Nocturnal Hemoglobinuria | Ulcerative Colitis | Extramammary Paget's Disease | Nanophthalmos | Avellino Corneal Dystrophy | Hereditary Pyropoikilocytosis | Colon Adenoma | Chorea-acanthocytosis | Microcephalic Osteodysplastic Primordial Dwarfism, Type I | Papillon-Lefevre Syndrome | Combined Pituitary Hormone Deficiency | Skin Papilloma | Urea Cycle Disorder | Hypothyroidism | Shwachman-Bodian-Diamond Syndrome | Familial Thoracic Aortic Aneurysm | Fundus Albipunctatus | Malaria, Cerebral | Sjogren Syndrome | Liver Failure, Acute Infantile | Guttate Psoriasis | Juvenile Hyaline Fibromatosis | PHARC Syndrome | Sarcoma, Alveolar Soft Part | Spinocerebellar Ataxia Type 14 | Infantile Spasm | Phosphoglycerate Dehydrogenase Deficiency | Aldosteronism | Myelofibrosis | D-2-Hydroxyglutaric Aciduria | Lymphoproliferative Disease, X-linked | Trichothiodystrophy | Spinocerebellar Ataxia Type 27 | Glycogen Storage Disease Type 3 | Prediabetes | Meckel-Gruber Syndrome | Acral Lentiginous Melanoma | Hennekam Lymphangiectasia-lymphedema Syndrome | Canavan Disease | Bruck Syndrome | Basal Ganglia Disease, Biotin-responsive | Hyperammonemia | Strabismus | Vestibular Disease | Eccrine Porocarcinoma | Hernia, Inguinal | Fuchs Heterochromic Iridocyclitis | Primary Biliary Cholangitis | Dystonia-parkinsonism, X-linked | Vitreoretinopathy, Proliferative | Peritonitis | Nephrocalcinosis | Panuveitis | Familial Hypertrophic Cardiomyopathy | Barrett Esophagus | FG Syndrome | Ectrodactyly | Oculocutaneous Albinism | Phenylketonuria II | Myeloid Leukemia | Familial Cerebral Amyloid Angiopathy | Neuropathy | Diarrhea | Stroke, Ischemic | Analgesia | Adenoma, Pituitary | Agranulocytosis | Fucosidosis | Cryptorchidism | Neuroendocrine Cancer | Diabetic Neuropathy | Aceruloplasminemia | Leukoplakia, Oral | Moyamoya Disease | Peripheral Neuropathy | Eclampsia | Disseminated Superficial Actinic Porokeratosis | Botulism | Pseudoachondroplasia | Platyspondylic Lethal Skeletal Dysplasia, Torrance Type | Spinocerebellar Ataxia Type 38 | Persistent Truncus Arteriosus | Monilethrix | Carey-Fineman-Ziter Syndrome | Bainbridge-Ropers Syndrome | Spinal And Bulbar Muscular Atrophy | Pierpont Syndrome | Leukocyte Adhesion Deficiency | Glaucoma | Hyperinsulinemia | Diabetic Macular Edema | TARP Syndrome | Tatton-Brown-Rahman Syndrome | Oligodendroglioma | Multiple System Atrophy | Gastroenteritis, Eosinophilic | Heart Failure | Peeling Skin Syndrome, Acral Type | Nance-Horan Syndrome | Dystonia Musculorum Deformans | Gangliosidosis, GM1 | Spastic Paraplegia Type 7 | Warsaw Breakage Syndrome | Aspergillosis | Paracoccidioidomycosis | Delirium | 5-oxoprolinase Deficiency | Corneal Dystrophy | Congenital Adrenal Hyperplasia | DNA Ligase IV Deficiency | Non-proliferative Diabetic Retinopathy | Osteogenesis Imperfecta | Biotinidase Deficiency | Hereditary Inclusion Body Myopathy | Familial Glucocorticoid 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Hyperthermia, Malignant | Progressive Familial Intrahepatic Cholestasis | Epidermolytic Palmoplantar Keratoderma | Cornelia De Lange Syndrome | Ganglioglioma | Scapuloperoneal Spinal Muscular Atrophy | Scleritis | Angelman Syndrome | Cerebral Cavernous Malformations | Lipid Storage Diseases | Pancytopenia | Recurrent Respiratory Papillomatosis | Adams-Oliver Syndrome | Wolfram Syndrome | Vertigo | Chronic Granulomatous Disease, X-linked | Cockayne Syndrome | Schistosomiasis | Hypolipoproteinemia | Whipple's Disease | Congenital Ichthyosiform Erythroderma | Myocarditis | Inflammatory Bowel Disease | Hypocalcemia | Carotid Artery Disease | Leri-Weill Dyschondrosteosis | Charcot-Marie-Tooth Disease Type 4B1 | Hypersensitivity | Beta-Propeller Protein-associated Neurodegeneration | Congenital Myopathy | Presbyopia | Hereditary Multiple Exostoses | Lymphoma, AIDS-related | Alagille Syndrome | Non-Langerhans Cell Histiocytosis | Inborn Errors Of Metabolism | Rickets | Heart Block | Chordoma | Postaxial Polydactyly | Optic Atrophy 2 | Thin Basement Membrane Disease | Congenital Disorders Of Glycosylation | Osteopetrosis | Hyperandrogenemia | Dysmorphophobia | WAGR Syndrome | N-acetylglutamate Synthase Deficiency | Hyperhomocysteinemia | Hemangioma | Jawad Syndrome | Proctitis | Hydronephrosis | Focal Dermal Hypoplasia | Vitreoretinal Degeneration, Snowflake Type | Mitochondrial DNA Depletion Syndrome, Hepatocerebral Form | Congenital Fiber-type Disproportion Myopathy | Meleda Disease | Cardiac Arrest | Left Ventricular Noncompaction | Hemophilia | Glycogen Storage Disease Type 1b | Histiocytosis | VACTERL/VATER Association | Hereditary Neuropathy With Liability To Pressure Palsies | Cholangitis | Marfan Syndrome | Growth Hormone Excess | Congenital Torticollis | Vascular Cognitive Impairment | Centronuclear Myopathy | Encephalitis | Pyruvate Carboxylase Deficiency Disease | Porphyria, Acute Intermittent | Bardet-Biedl Syndrome | Dyskeratosis Congenita | Progressive 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