Tularemia
Tularemia
About the Disease
Tularemia, also known as francisella tularensis infection, is related to oculoglandular tularemia and ulceroglandular tularemia. An important gene associated with Tularemia is SLC11A1 (Solute Carrier Family 11 Member 1), and among its related pathways/superpathways are MIF Mediated Glucocorticoid Regulation and Innate Immune System. The drugs Immunologic Factors and Vaccines have been mentioned in the context of this disorder. Affiliated tissues include skin, lung and brain, and related phenotypes are fever and arthralgia
Common Targets
PDPK1 | TRPA1 | TRPV3 | Heat shock protein 70 (nonspecified subtype) | TLR3 | Heat shock protein 90 (nonspecified subtype) | NR3C1
![疾病靶点研报](../img/disease-target-analysis-report.jpg)
Note: If you'd like to get a target analysis report for Tularemia, 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 Tularemia at a cost 90% lower than traditional approaches, please feel free to contact us at BD@silexon.ai.
Other Diseases
Triple A Syndrome | Sarcoma, Endometrial Stromal | Waardenburg Syndrome Type 2A | Hermansky-Pudlak Syndrome | Hypopigmentation | Primary Carnitine Deficiency | Ophthalmia, Sympathetic | Proximal Symphalangism | Blue Rubber Bleb Nevus Syndrome | Myositis, Focal | Neural Tube Defect | Granular Corneal Dystrophy | Chronic Neutrophilic Leukemia | Carcinoma, Small Cell | Hypothalamic Obesity | Ophthalmoplegia | Keratocystic Odontogenic Tumor | Apert Syndrome | Cholesteryl Ester Storage Disease | Peters-plus Syndrome | Tuberculous Meningitis | Ameloblastic Carcinoma | Hyperthyroidism | Congenital Disorders Of Glycosylation | Castleman Disease | 3-hydroxy-3-methylglutaric Aciduria | Hypertension, Pulmonary | Mevalonate Kinase Deficiency | Cutaneous Angiosarcoma | Hyperthermia, Malignant | Mandibuloacral Dysplasia With Type A Lipodystrophy | Spinal Muscular Atrophy With Progressive Myoclonic Epilepsy | Sickle Cell Anemia | Infantile Neuroaxonal Dystrophy | Schwannomatosis | Hydrolethalus Syndrome | Encephalopathy, Hepatic | Cholelithiasis | Hereditary Sensory And Autonomic Neuropathy | Cellulitis | Diarrhea | Craniosynostosis | Hyperkeratosis | Tinea Versicolor | Adenoid Cystic Carcinoma | Pneumonia, Bacterial | Walker-Warburg Syndrome | Pregnancy, Ectopic | Chediak-Higashi Syndrome | Paget's Disease Of The Breast | Glycogen Storage Disease Type 3 | Celiac Disease | Wiedemann-Steiner Syndrome | Renal Medullary Carcinoma | Antley-Bixler Syndrome | Platelet Disorders | Sulfite Oxidase Deficiency | Leri-Weill Dyschondrosteosis | Charcot-Marie-Tooth Disease | Hereditary Spastic Paraplegia | Kabuki Syndrome 2 | Rubeosis Iridis | Glanzmann Thrombasthenia | Spinocerebellar Ataxia Type 27 | Tic Disorder | Sclerosteosis 2 | Transthyretin-related Amyloidosis | Familial Hypertrophic Cardiomyopathy | Eosinophilic Asthma | Hemorrhoids | Nance-Horan Syndrome | Thalassemia | Posterior Polar Cataract | Thrombosis | Anorexia Nervosa | Heterotopic Ossification | Facioscapulohumeral Muscular Dystrophy Type 1 | Greig Cephalopolysyndactyly Syndrome | Lipid Storage Myopathy | Sarcoma, Alveolar Soft Part | Neurofibromatosis Type 1 | Carpenter Syndrome | Congenital Poikiloderma | Irritable Bowel Syndrome | Major Depression | Pseudohypoparathyroidism Type 1B | Viral Meningitis | Autosomal Recessive Spastic Paraplegia Type 75 | Pulmonary Vein Stenosis | Leukemia-lymphoma, Adult T-cell | Varicocele | Mixed Connective Tissue Disease | Chronic Leukemia | 3-methylglutaconic Aciduria Type I | Polycystic Kidney, Autosomal Recessive | Neurofibromatosis-Noonan Syndrome | Thrombocythemia, Essential | Acromegaly | Diabetes Gestational | Abetalipoproteinemia | Congenital Diaphragmatic Hernia | Venous Insufficiency | MIRAGE Syndrome | Encephalitis | Porphyria, Acute Intermittent | Trigonocephaly | ACTH-independent Macronodular Adrenal Hyperplasia | Crigler-Najjar Syndrome | Cardiospondylocarpofacial Syndrome | Jacobsen Syndrome | Premenstrual Syndrome | Necrotizing Autoimmune Myopathy | Familial Isolated Hyperparathyroidism | CHOPS Syndrome | TARP Syndrome | Acromesomelic Dysplasia | Coffin-Siris Syndrome | Crouzon Syndrome With Acanthosis Nigricans | Osteitis | Schaaf-Yang Syndrome | Motor Neuron Diseases | Sleep Apnea | Dysferlinopathy | Hyperuricemia | Gnathodiaphyseal Dysplasia | Epidermolysis Bullosa | Spinocerebellar Ataxia Type 23 | Ischemia | Skin Papilloma | Mucolipidosis Type IV | Metaphyseal Chondrodysplasia, Schmid Type | Blue Nevus | Von Willebrand Disease | Endometriosis | Cancer, Skin | Hepatic Adenomatosis | LEOPARD Syndrome | NGLY1 Deficiency | Microcephaly | Neonatal Progeroid Syndrome | Hypereosinophilic Syndrome | LMNA-related Congenital Muscular Dystrophy | Antisocial Personality Disorder | Spinocerebellar Ataxia Type 20 | Lateral Meningocele Syndrome | Inborn Errors Of Metabolism | Phosphoglycerate Dehydrogenase Deficiency | Cherubism | Alazami Syndrome | Waldenstrom Macroglobulinemia | Cranioectodermal Dysplasia | Isovaleric Acidemia | Lymphedema-distichiasis Syndrome | Dubin-Johnson Syndrome | Thanatophoric Dysplasia | Encephalitis, Tick-borne | Interstitial Lung Diseases | Chylothorax, Congenital | Episodic Ataxia | Lymphopenia | Acute Tubular Necrosis | Dent Disease | Takotsubo Cardiomyopathy | Ganglioneuroma | Pneumoconiosis | Borjeson-Forssman-Lehmann Syndrome | Meningitis | Retinal Telangiectasia | Fetal Alcohol Syndrome | X-linked Myotubular Myopathy | Usher Syndrome Type I | Frank-ter Haar Syndrome | Tenosynovial Giant Cell Tumor | Common Variable Immunodeficiency | Barakat Syndrome | Melanoma | Norrie Disease | Diabetes Insipidus, Neurogenic | Myeloid Leukemia | Malignant Peripheral Nerve Sheath Tumor | Blepharo-cheilo-odontic Syndrome | Pneumonia, Viral | Pemphigus | Reflex Epilepsy | Bicuspid Aortic Valve | Bipolar Disorder | Heroin Dependence | Esotropia | Macrophagic Myofasciitis | Urolithiasis | 17-beta-hydroxysteroid Dehydrogenase X Deficiency | Sweet Syndrome | Pyruvate Kinase Deficiency | Apparent Mineralocorticoid Excess Syndrome | Glioma | Fanconi Syndrome | Hyperbilirubinemia, Neonatal | Thrombasthenia | Rolandic Epilepsy | Cabezas Syndrome | Thanatophoric Dysplasia Type 1 | Leri Pleonosteosis | Thrombophilia | Diabetes Type 1 | McCune-Albright Syndrome | Megaloblastic Anemia | Eosinophilia | 3-hydroxyacyl-CoA Dehydrogenase Deficiency | Tietze Syndrome | Aspartylglycosaminuria | Congenital Hereditary Endothelial Dystrophy Type I | Guillain-Barre Syndrome | Chudley-McCullough Syndrome | Ganglioglioma | Holoprosencephaly | Congenital Disorders Of Glycosylation Type II | Syndactyly | Charcot-Marie-Tooth Disease Type 2E | Chylomicron Retention Disease | Congenital Adrenal Hyperplasia 1 | Keratoconus | Strabismus | Epidermolytic Hyperkeratosis | Reye Syndrome | Adenoma, Pituitary | GM2-gangliosidosis AB Variant | Progressive Encephalopathy-optic Atrophy Syndrome | Nemaline Myopathy | Pseudohypoparathyroidism Type 1A | Methemoglobinemia | Lymphoproliferative Disorders | Nevus | Anorectal Malformations | Congenital Hypofibrinogenemia | Actinomycetoma | Macular Corneal Dystrophy | Cystitis, Interstitial | Pouchitis | Asplenia | Aspergillosis | Pontocerebellar Hypoplasia | Retinitis | Beckwith-Wiedemann Syndrome | Juvenile Hyaline Fibromatosis | COACH Syndrome | Aarskog-Scott Syndrome | Hypertrophic Osteoarthropathy, Primary, Autosomal Recessive 1 | Coronary Artery Disease | Enlarged Vestibular Aqueduct | Epidermolysis Bullosa Simplex, Dowling-Meara Type | Usher Syndrome Type II | Lymphangioleiomyomatosis | Nephrocalcinosis | Neuroblastoma | Neuromuscular Disorders | Hepatitis | Nestor-Guillermo Progeria Syndrome | Chromosome 17q21.31 Deletion Syndrome | Spinal Muscular Atrophy Type 3 | Ichthyosis | Sepiapterin Reductase Deficiency | Pneumonia, Mycoplasma | Waardenburg Syndrome Type 4A | Eczema | B-cell Prolymphocytic Leukemia | NDH Syndrome | Early Infantile Epileptic Encephalopathy 1 | Arteriovenous Malformations | Bronchiolitis | Dementia | Amenorrhea | Papillon-Lefevre Syndrome | Pigment Dispersion Syndrome | Autism Spectrum Disorders | Hemolytic Anemia | Otitis Externa | Neurofibroma, Plexiform | Hemochromatosis Type 1 | Epidermal Nevus Syndrome | Epidermolytic Palmoplantar Keratoderma | Double Outlet Right Ventricle | Pantothenate Kinase-associated Neurodegeneration | Lyme Disease | Hemolytic Uremic Syndrome, Atypical | Atopy | Hypersomnia | Porphyria, Variegate | Carcinoma, Merkel Cell | Acute Chest Syndrome | Limb Girdle Muscular Dystrophy | Filariasis | Pierson Syndrome | Uveitis | Schuurs-Hoeijmakers Syndrome | Microcephalic Osteodysplastic Primordial Dwarfism, Type II | Intracranial Hypertension | Non-epidermolytic Palmoplantar Keratoderma | Rheumatoid Arthritis | Nemaline Myopathy 10 | Spinocerebellar Ataxia Type 13 | Multiple Sulfatase Deficiency | Vitamin A Deficiency | Pulmonary Alveolar Microlithiasis | Rubinstein-Taybi Syndrome | Basal Cell Nevus Syndrome | Choroiditis | Bronchitis | Withdrawal Syndrome | Pleurisy | Hemochromatosis | Albinism | Sclerocornea | Prolidase Deficiency | Neurofibroma | Neuroendocrine Cancer | Thyroid Hormone Resistance | Gestational Trophoblastic Disease | Prune Belly Syndrome | PASLI Disease | 3-methylglutaconic Aciduria | Atherosclerosis | Osteoporosis | Carbohydrate Metabolism Disorders | Familial Hypobetalipoproteinemia | Episodic Ataxia Type 1 | Rhizomelic Chondrodysplasia Punctata | Nasodigitoacoustic Syndrome | Retinitis Pigmentosa 3 | Leprosy | Traboulsi Syndrome | Kidney Stones | Neuromyelitis Optica | Diabetic Macular Edema | McLeod Syndrome | Pulmonary Stenosis | Osteogenesis Imperfecta Type VI | Thyroid Dyshormonogenesis | Hemangioendothelioma | Xeroderma Pigmentosum | Neurocysticercosis | Multiple Hamartoma Syndrome | Hemophilia | Neurocutaneous Syndromes | Myofibrillar Myopathy | Necrobiosis Lipoidica | Peripheral T-cell Lymphoma | Partington Syndrome | Diabetic Nephropathy | Localized Scleroderma | Myoclonus | Jalili Syndrome | Usher Syndrome Type III | Neuroma | Zygomycosis | Scleroderma | DNA Ligase IV Deficiency | Brenner Tumor | Thromboembolism | Cold Agglutinin Disease | Plasma Cell Dyscrasia | Charcot-Marie-Tooth Disease Type 2T | Antithrombin III Deficiency | Mitochondrial DNA Depletion Syndrome | Hemoglobinopathies | Distal Myopathy 2 | Heimler Syndrome | Infectious Diarrhea | Spinal Muscular Atrophy | Craniofacial Dysostosis | Medulloblastoma | Familial Male-limited Precocious Puberty | Fanconi Anemia | Panuveitis | Hyperostosis | Pulmonary Alveolar Proteinosis | Giant Cell Arteritis | Best Macular Dystrophy | Cryptosporidiosis | Lymphoma, B-cell | Focal Segmental Glomerulosclerosis | Infertility | Chronic Myelomonocytic Leukemia | Depression | Bainbridge-Ropers Syndrome | Chronic Idiopathic Myelofibrosis | MELAS Syndrome | Carney-Stratakis Syndrome | Glucagonoma | Ectopia Lentis, Isolated, Autosomal Recessive | Spinocerebellar Ataxia Type 8 | Glaucoma, Congenital | Klinefelter Syndrome | Lymphomatoid Granulomatosis | Alopecia | Hyperinsulinism-hyperammonemia Syndrome | Kaposiform Hemangioendothelioma | Ureteropelvic Junction Obstruction | Presbyopia | Acne | Stickler Syndrome