Papulopustular Rosacea

About the Disease
Rosacea, also known as erythematotelangiectatic rosacea, is related to telangiectasis and acne, and has symptoms including exanthema and pruritus. An important gene associated with Rosacea is CAMP (Cathelicidin Antimicrobial Peptide), and among its related pathways/superpathways are Innate Immune System and Disease. The drugs Metronidazole and Minocycline have been mentioned in the context of this disorder. Affiliated tissues include skin, eye and pituitary, and related phenotypes are no effect and no effect

Common Targets
Importin alpha/beta-1 | G7295 | Matrix Metalloproteinase (MMP) (nonspecified subtype) | TYR | TRPM8 | G142 | Chloride channel (nonspecified subtype) | TRPV2 | NR1I2 | TRPV1 | Platelet-Derived Growth Factor Receptor (nonspecified subtype) | OSBP | TRPA1 | Proteasome Complex | KDR | Fibroblast Growth Factor Receptor (FGFR) (nonspecified subtype) | GPR55 | Vascular endothelial growth factors (VEGF) (nonspecified subtype)

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

Other Diseases

Hyperbilirubinemia, Neonatal | Multiple Sclerosis, Chronic Progressive | Porphyria, Variegate | Medulloblastoma | Acrodermatitis Enteropathica | Spitzoid Melanoma | Weill-Marchesani Syndrome | Myofibromatosis | Kearns-Sayre Syndrome | Anencephaly | Multiple Myeloma | Parkinson's Disease | Usher Syndrome | Erythromelalgia | Nestor-Guillermo Progeria Syndrome | Hemophilia | Inflammatory Bowel Disease | Congenital Disorders Of Glycosylation Type II | Infertility | Diamond-Blackfan Anemia | Paraganglioma | Amblyopia | Holt-Oram Syndrome | Neutropenia | Alpha-1 Antitrypsin Deficiency | Thrombophilia | Chronic Leukemia | Intestinal Hypomagnesemia 1 | Poirier-Bienvenu Neurodevelopmental Syndrome | Speech Disorders | Hidradenitis Suppurativa | Cancer, Skin | Krabbe Disease | Familial Thoracic Aortic Aneurysm | Ventricular Septal Defect | Mitochondrial Disease | Amelanotic Melanoma | Chordoma | Japanese Encephalitis | Oculocutaneous Albinism | Retinoblastoma | Lennox-Gastaut Syndrome | Niemann-Pick Disease, Type C | Hemorrhagic Disorders | Werner's Syndrome | Cerebrotendinous Xanthomatosis | Glycogen Storage Disease | Encephalitis, Tick-borne | Ameloblastic Carcinoma | Postpartum Depression | Oligodendroglioma | Eiken Syndrome | Skin Papilloma | Scapuloperoneal Spinal Muscular Atrophy | Lymphoma Lymphoblastic | Acute Myeloid Leukemia | Keratitis | Renal Tubular Dysgenesis | Periventricular Nodular Heterotopia | Patent Foramen Ovale | Multiple Epiphyseal Dysplasia | Motor Neuron Diseases | Myotonia | Spinocerebellar Ataxia Type 8 | Plasma Cell Leukemia | Von Willebrand Disease | Birt-Hogg-Dube Syndrome | Crigler-Najjar Syndrome | Chronic Beryllium Disease | Liver Diseases | Left Ventricular Noncompaction | Liver Failure | Citrullinemia | Stargardt Disease | Wilson's Disease | Peritonitis | Tyrosine Hydroxylase Deficiency | Saethre-Chotzen Syndrome | Guillain-Barre Syndrome | Chronic Kidney Disease | Cholera | Menetrier Disease | Carpenter Syndrome | Lathosterolosis | Vertebrobasilar Insufficiency | Acquired Partial Lipodystrophy | Antenatal Bartter Syndrome Type 1 | Diffuse Palmoplantar Keratoderma | Autosomal Recessive Spastic Paraplegia Type 35 | X-linked Acrogigantism | Prune Belly Syndrome | Peutz-Jeghers Syndrome | Still Disease | Hereditary Pyropoikilocytosis | Pityriasis Rubra Pilaris | Trismus-pseudocamptodactyly Syndrome | Usher Syndrome Type IIC | Chronic Neutrophilic Leukemia | Antisocial Personality Disorder | Congenital Nephrotic Syndrome | Constipation | Guanidinoacetate Methyltransferase Deficiency | Thyroid Dysgenesis | Demyelinating Diseases | Gaze Palsy, Familial Horizontal, With Progressive Scoliosis, 2 | Atopy | Pouchitis | Sjogren Syndrome | Androgen Insensitivity | Specific Granule Deficiency | Hypoglycemia | Granular Corneal Dystrophy | Hyperacusis | Oguchi Disease-2 | Frontotemporal Dementia | Sezary Syndrome | Gray Platelet Syndrome | Mucolipidosis Type IV | Asthma | Renal Tubular Acidosis | Oculocutaneous Albinism Type 1 | Creatine Deficiency Syndrome Due To AGAT Deficiency | Orotic Aciduria | Aarskog-Scott Syndrome | Uremia | Infantile Liver Failure Syndrome 1 | Pycnodysostosis | Giant Cell Arteritis | Leukemia-lymphoma, Adult T-cell | Exocrine Pancreatic Insufficiency | Cyst | Infantile Nephropathic Cystinosis | Diffuse Mesangial Sclerosis | Ectodermal Dysplasia | Hypertension, Pulmonary | Intestinal Obstruction | Myocardial Infarction | Aneurysm, Thoracic Aortic | Down Syndrome | Cryptosporidiosis | Spinocerebellar Ataxia Type 38 | Sengers Syndrome | Tendinopathy | Cutaneous Mastocytosis | Combined Pituitary Hormone Deficiency | Chorea | Lissencephaly 2 | Cervical Dystonia | Restless Legs Syndrome | Alcoholism | Calcium Pyrophosphate Deposition Disease | Branchiootorenal Syndrome | Cardiac Arrest | Sarcoma | Hernia, Inguinal | Overactive Bladder | Spinal Muscular Atrophy Type 2 | Congenital Hereditary Endothelial Dystrophy Type I | Malignant Fibrous Histiocytoma | Disseminated Intravascular Coagulation | Malignant Peripheral Nerve Sheath Tumor | Meesmann Corneal Dystrophy | Optic Nerve Hypoplasia, Bilateral | Limb Girdle Muscular Dystrophy | Pseudoachondroplasia | Asthma, Exercise-induced | Cerebellar Ataxia, Cayman Type | Orthostatic Intolerance | Chylomicron Retention Disease | Cold-induced Sweating Syndrome | Angiosarcoma | Mandibuloacral Dysplasia With Type A Lipodystrophy | Congenital Ichthyosiform Erythroderma | Schnitzler Syndrome | Loeys-Dietz Syndrome Type 4 | GATA2 Deficiency | Epidermolysis Bullosa Simplex | Stickler Syndrome | Relapsing Polychondritis | Generalized Epilepsy And Paroxysmal Dyskinesia | Aspartylglycosaminuria | Dystonia-parkinsonism, X-linked | DiGeorge Syndrome | Pierre Robin Syndrome | Urea Cycle Disorder | Hypoplastic Left Heart Syndrome | Spinocerebellar Ataxia Type 23 | Salla Disease | Hypophosphatemic Rickets, Autosomal Recessive, 1 | Hemolytic Uremic Syndrome, Atypical | Neuronal Ceroid Lipofuscinosis | Arthritis, Psoriatic | Arterial Tortuosity Syndrome | Primary Sclerosing Cholangitis | Fanconi Anemia | Carpal Tunnel Syndrome | Fundus Albipunctatus | Evans Syndrome | Chondrodysplasia Punctata | Vasculitis | Conduct Disorder | C3 Glomerulopathy | Osteoporosis | Antley-Bixler Syndrome | Ovarian Hyperstimulation Syndrome | Atopic Dermatitis | Twin-to-twin Transfusion Syndrome | Veno-occlusive Disease | Fetal And Neonatal Alloimmune Thrombocytopenia | Burn-McKeown Syndrome | Trachoma | Retinal Dystrophy | Pemphigoid | Acromegaly | Hypophosphatemic Rickets With Hypercalciuria, Hereditary | Fukuyama Congenital Muscular Dystrophy | Pseudo-pseudohypoparathyroidism | Multiple Sclerosis, Relapsing-remitting | Sertoli Cell-only Syndrome | Epilepsy, Generalized | Ghosal Syndrome | Urofacial Syndrome | Apraxia | Irritable Bowel Syndrome | Dystonia Musculorum Deformans | Panic Disorder | Rett Syndrome | Stromal Corneal Dystrophy | Gastritis | Cramp Fasciculation Syndrome | Chronic Periodontitis | Syndactyly | Rhinitis | Achromatopsia | Tinea Versicolor | Bronchitis | Carbohydrate Metabolism Disorders | Photosensitivity | Cryopyrin-associated Periodic Syndromes | Corneal Dystrophy | Renal Medullary Carcinoma | Kidney Stones | Mastitis | Bullous Pemphigoid | Goiter, Nodular | Waardenburg Syndrome Type 2A | Tremor | Chondrodysplasia Punctata 1, X-linked Recessive | Partington Syndrome | Congenital Dysfibrinogenemia | Acromicric Dysplasia | Gastroenteritis, Eosinophilic | Subcortical Band Heterotopia | Congenital Hypofibrinogenemia | Premature Ejaculation | Autosomal Recessive Spastic Paraplegia Type 75 | Kleine-Levin Syndrome | Adrenomyeloneuropathy | Liddle Syndrome | Fabry's Disease | Tietze Syndrome | Rhizomelic Chondrodysplasia Punctata | T-cell Prolymphocytic Leukemia | Diabetes Insipidus, Neurogenic | Primrose Syndrome | Alveolar Capillary Dysplasia | Myhre Syndrome | Diabetes | Macrodactyly | Hereditary Sensory And Autonomic Neuropathy | Renal Failure | Distal Myopathy | Paronychia | Avian Influenza | Thanatophoric Dysplasia Type 1 | Hepatitis A | Varicocele | Optic Neuropathy, Anterior Ischemic | Autoimmune Disease | Primary Hyperoxaluria | Endometrial Hyperplasia | Endometritis | Babesiosis | Tracheal Disorders | Hereditary Multiple Exostoses | Juvenile Myoclonic Epilepsy | Spastic Paraplegia Type 7 | Brenner Tumor | Delirium | Leber Congenital Amaurosis | Acute Kidney Injury | Congenital Dyserythropoietic Anemia Type 4 | Gastrointestinal Disorders | Congenital Myasthenic Syndrome | Nicotine Dependence | 3C Syndrome | Methylmalonic Aciduria And Homocystinuria, CblC Type | Spinocerebellar Ataxia Type 17 | Plasmacytoma | Galactosemia | Neurodevelopmental Disorder With Central Hypotonia And Dysmorphic Facies | Beare-Stevenson Syndrome | SAPHO Syndrome | Leishmaniasis, Cutaneous | Osteonecrosis | Hemorrhoids | Molybdenum Cofactor Deficiency | Keratosis, Seborrheic | Osteoarthritis | Porphyria, Acute Intermittent | Otosclerosis | Wolfram Syndrome | Takotsubo Cardiomyopathy | 3-methylglutaconic Aciduria Type I | Adrenal Insufficiency | Pernicious Anemia | Metachromatic Leukodystrophy | Osmotic Demyelination Syndrome | Papilloma | Cancer, Colon | Nephronophthisis | Influenza | Autoimmune Polyendocrinopathy Syndrome Type I | Chronic Myelomonocytic Leukemia | Cholestasis, Intrahepatic | Ileitis | Polydactyly | Hypogonadism | Scleritis | Fibromuscular Dysplasia | Scapuloperoneal Myopathy, X-linked Dominant | Hemorrhage | Follicular Dendritic Cell Sarcoma | Enlarged Vestibular Aqueduct | Peroxisomal Disorder | Hepatic Veno-occlusive Disease | L-2-Hydroxyglutaric Aciduria | Woodhouse-Sakati Syndrome | Oculocutaneous Albinism Type 4 | Gangliosidosis | Dwarfism | Renal Dysplasia | Epilepsy | Anorchia | Uterine Leiomyoma | Waardenburg Syndrome Type 1 | Panniculitis | Chromosome 9q34.3 Deletion Syndrome | Hypophosphatasia | VACTERL/VATER Association | Pierson Syndrome | Meckel-Gruber Syndrome | Atelosteogenesis Type 2 | Dowling-Degos Disease | Cardiac Sarcoidosis | Lipodystrophy | Encephalopathy, Hepatic | Spinocerebellar Ataxia Type 40 | Hydrops Fetalis | Lymphangioleiomyomatosis | Scabies | Acute Generalized Exanthematous Pustulosis | Lewy Body Dementia | Williams Syndrome | Acne | Tibial Muscular Dystrophy | Spinocerebellar Ataxia Type 13 | Congenital Myopathy | Dystonia | Familial Advanced Sleep Phase Syndrome | Hypereosinophilic Syndrome | Stroke, Hemorrhagic | Pleurisy | Non-proliferative Diabetic Retinopathy | Auriculocondylar Syndrome | Micro Syndrome | Mitochondrial DNA Depletion Syndrome | Multiple Sclerosis, Primary Progressive | Growth Hormone Excess | Cardiomyopathy, Hypertrophic | Lymphangiomatosis | Basal Ganglia Disease, Biotin-responsive | Nance-Horan Syndrome | Neuromyotonia | Benign Recurrent Intrahepatic Cholestasis 1 | LEOPARD Syndrome | Gardner Syndrome | Gangliosidosis, GM1 | Heterotaxy | Mohr-Tranebjaerg Syndrome | Hepatitis, Chronic | Cenani-Lenz Syndactyly Syndrome | Pneumonia, Mycoplasma | Fibrosis | Hyperphenylalaninemia | Autism Spectrum Disorders | Hydrocephalus, Normal Pressure | Astrocytoma | Periodontitis | Spondylosis