Disease

Aspergillosis

About the Disease
Aspergillosis, also known as aspergillosis, susceptibility to, is related to allergic bronchopulmonary aspergillosis and invasive aspergillosis, and has symptoms including fever and pruritus. An important gene associated with Aspergillosis is CLEC7A (C-Type Lectin Domain Containing 7A), and among its related pathways/superpathways are ERK Signaling and Innate Immune System. The drugs Guaifenesin and Cathine have been mentioned in the context of this disorder. Affiliated tissues include lung, kidney and skin, and related phenotypes are cough and positive blood 1,3 beta glucan test

Common Targets
CD209 | CLEC7A | G7422 | G114548 | PPBP | CYP2C19 | G6774 | PTX3 | ARNT2 | FKBP1A | G7099 | DHODH | DENND1B | PLAT | CXCL10 | TLR9 | TLR1

疾病靶点研报
Aspergillosis

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

Other Diseases

Saethre-Chotzen Syndrome | Lipid Metabolism Disorders | Intracerebral Hemorrhage | LEOPARD Syndrome | Focal Segmental Glomerulosclerosis | Charcot-Marie-Tooth Disease, Type 6 | Neurocutaneous Melanocytosis | Tardive Dyskinesia | Vertebrobasilar Insufficiency | Esophageal Carcinoma | Enterocolitis, Necrotizing | Donnai-Barrow Syndrome | Dowling-Degos Disease | Metanephric Adenoma | Sleep Disorder | Tibial Muscular Dystrophy | Lipid Storage Myopathy | Fraser Syndrome | Gastroenteritis, Eosinophilic | Lymphoproliferative Disease, X-linked | Pulmonary Tuberculosis | Hypertensive Retinopathy | Majeed Syndrome | Giant Cell Glioblastoma | Pseudohypoparathyroidism Type 1B | Progressive Familial Intrahepatic Cholestasis Type 3 | Agoraphobia | Microphthalmia, Syndromic 7 | Dermatitis Herpetiformis | Megalencephaly | Cystitis | Antenatal Bartter Syndrome Type 1 | Focal Facial Dermal Dysplasia | Erythrokeratodermia Variabilis | Osteopetrosis | Sweet Syndrome | Primary Hyperoxaluria | Marfan Syndrome | Hypogonadism | Spinocerebellar Ataxia Type 1 | Neuroectodermal Tumors, Primitive | Tricho-hepato-enteric Syndrome | SAPHO Syndrome | Familial Isolated Hyperparathyroidism | Lactose Intolerance | Pituitary Stalk Interruption Syndrome | Periodontitis | Hepatic Steatosis | Cardiomyopathy, Hypertrophic | Antley-Bixler Syndrome | Familial Exudative Vitreoretinopathy | Hypophosphatasia | Acute Generalized Exanthematous Pustulosis | Still Disease | Conjunctivitis, Allergic | Galloway-Mowat Syndrome | Triphalangeal Thumb-polysyndactyly Syndrome | Myositis | Congenital Primary Aphakia | Urofacial Syndrome | Toxoplasmosis | Tylosis With Esophageal Cancer | Interstitial Lung Diseases | Smith-Magenis Syndrome | Hyperkeratosis | Hypertrophic Osteoarthropathy, Primary, Autosomal Recessive 2 | Pityriasis Rubra Pilaris | Adult Polyglucosan Body Disease | Optic Neuropathy, Anterior Ischemic | Pulmonary Capillary Hemangiomatosis | Anuria | Mevalonate Kinase Deficiency | Saul-Wilson Syndrome | Dysgerminoma | Cyst | Cellulitis | Veno-occlusive Disease | Sezary Syndrome | Hypomyelination With Atrophy Of Basal Ganglia And Cerebellum | Polymicrogyria | Guanidinoacetate Methyltransferase Deficiency | Enhanced S-cone Syndrome | Cluster Headache | Compartment Syndrome | B-cell Prolymphocytic Leukemia | Neuroblastoma | Prolactinoma | MIRAGE Syndrome | Glycogen Storage Disease Type 4 | Dystrophy, Cone-rod | Melnick-Needles Syndrome | Superficial Spreading Melanoma | Trichothiodystrophy | Pneumonia, Viral | Alopecia | Trichomegaly | Scleritis | Endocarditis | Congenital Myasthenic Syndrome | Wolfram Syndrome | Facioscapulohumeral Muscular Dystrophy Type 1 | Encephalocele | Gastroschisis | Agammaglobulinemia | Hypertriglyceridemia | Corneal Dystrophies, Hereditary | Von Hippel-Lindau Disease | Cerebrovascular Disorders | Usher Syndrome Type III | Motion Sickness | Patent Foramen Ovale | Creatine Deficiency Syndrome | Fibrodysplasia Ossificans Progressiva | Vogt-Koyanagi-Harada Syndrome | Spitzoid Melanoma | Brenner Tumor | Lipid Storage Diseases | Craniosynostosis | GM2-gangliosidosis AB Variant | Protein S Deficiency | Glycogen Storage Disease Type 0 | Adrenomyeloneuropathy | Retinal Degeneration | Pseudohypoaldosteronism | Menetrier Disease | Aldosterone Synthase Deficiency | Venous Insufficiency | Imerslund-Grasbeck Syndrome | Adenomyosis | Waardenburg Syndrome | Cancer, Brain | Dyskeratosis Congenita | Apert Syndrome | Rheumatoid Arthritis | Meniere's Disease | Vitreoretinal Degeneration, Snowflake Type | Heterotaxy | Meningococcal Infections | Castleman Disease | Anxiety Disorders | Hypertelorism | Nijmegen Breakage Syndrome | Chronic Beryllium Disease | Sjogren Syndrome | Postpoliomyelitis Syndrome | Hypertension, Pulmonary | Spinocerebellar Ataxia Type 7 | Familial Partial Lipodystrophy | Vitamin K Deficiency | Chromosome 9q34.3 Deletion Syndrome | Acrodermatitis Enteropathica | Abetalipoproteinemia | Malignant Peripheral Nerve Sheath Tumor | Neonatal Progeroid Syndrome | Loeys-Dietz Syndrome | Hepatitis | Retinal Dystrophy | Lassa Fever | Amelanotic Melanoma | Pulverulent Zonular Cataract | Osteogenesis Imperfecta Type II | Bleeding Disorder Due To CalDAG-GEFI Deficiency | Nemaline Myopathy 10 | Acromegaly | Arts Syndrome | Hidradenitis | Nail Disorder, Nonsyndromic Congenital | Nail-Patella Syndrome | Multiple Sclerosis, Chronic Progressive | Tremor | Learning Disability | Birt-Hogg-Dube Syndrome | Psoriasis | Olmsted Syndrome | Alopecia Totalis | Early Infantile Epileptic Encephalopathy 1 | Urethritis | Anovulation | Adenocarcinoma | Epidermolysis Bullosa Dystrophica | T-cell Prolymphocytic Leukemia | Kashin-Beck Disease | Arteriovenous Malformations | Congenital Heart Defects | Encephalopathy, Ethylmalonic | Hodgkin Lymphoma | Myasthenia Gravis | Vitreoretinopathy, Proliferative | Priapism | Atelosteogenesis Type 1 | Sick Sinus Syndrome 1 | Schistosomiasis | Central Pain Syndrome | Obesity | Atherosclerosis | Brachial Plexus Neuropathy | Autosomal Recessive Spastic Paraplegia Type 54 | Bacterial Meningitis | Bone Giant Cell Tumor | Schizoaffective Disorder | Benign Recurrent Intrahepatic Cholestasis 1 | Kabuki Syndrome 2 | D-2-Hydroxyglutaric Aciduria | Thalassemia | Porphyria Cutanea Tarda | Scoliosis | Skin Carcinoma | Blastomycosis | Carbamoyl Phosphate Synthetase I Deficiency | Low Tension Glaucoma | Tetraplegia | Fontaine Progeroid Syndrome | Shwachman-Bodian-Diamond Syndrome | Low Phospholipid Associated Cholelithiasis | Sengers Syndrome | Uterine Leiomyoma | Familial Episodic Pain Syndrome | Amblyopia | Exotropia | Postpartum Depression | Epidermolysis Bullosa Acquisita | Myopia | Familial Hypertrophic Cardiomyopathy | Insulinoma | Schizencephaly | DEND Syndrome | Nicotine Addiction | Plasma Cell Leukemia | Hermansky-Pudlak Syndrome | Fatty Aldehyde Dehydrogenase Deficiency | Long QT Syndrome Type 2 | Trichotillomania | Ameloblastoma | Dystonia Musculorum Deformans | Familial Digital Arthropathy-brachydactyly | Treacher Collins Syndrome | Progressive Encephalopathy-optic Atrophy Syndrome | Ornithine Transcarbamylase Deficiency | Autonomic Neuropathy | Hereditary Hemorrhagic Telangiectasia | Congenital Hereditary Endothelial Dystrophy Type II | Cystitis, Interstitial | Retinoschisis | Tietze Syndrome | Charcot-Marie-Tooth Disease Type 3 | Obesity, Morbid | Scapuloperoneal Myopathy, X-linked Dominant | Cartilage Disorders | 3C Syndrome | Ebstein Anomaly | Blue Rubber Bleb Nevus Syndrome | Dental Caries | Pernicious Anemia | High Molecular Weight Kininogen Deficiency | H Syndrome | Parvovirus B19 Infection | Pneumococcal Meningitis | Thrombophilia | Ichthyosis Hystrix, Curth-Macklin Type | Thrombocythemia, Essential | Pilomatrix Carcinoma | Acanthosis Nigricans | Early Infantile Epileptic Encephalopathy 4 | Keratosis, Actinic | Schuurs-Hoeijmakers Syndrome | Sporadic Hemiplegic Migraine | Diffuse Palmoplantar Keratoderma | Hypogammaglobulinemia | Wiedemann-Steiner Syndrome | Heavy Chain Disease | Hypohidrotic Ectodermal Dysplasia | Autoimmune Polyendocrinopathy Syndrome Type I | Anencephaly | Dent Disease | Pulmonary Stenosis | Aphasia | Histiocytic Sarcoma | Rhabdomyosarcoma, Embryonal | Persistent Hyperplastic Primary Vitreous | Desbuquois Syndrome | Nephrocalcinosis | Skin Papilloma | Hyperphosphatasia With Intellectual Disability Syndrome 4 | Thromboembolism | Sialidosis | Hemangioblastoma | Schwartz-Jampel-Aberfeld Syndrome | Congenital Hypofibrinogenemia | Adenoma, Pleomorphic | Pseudohypoparathyroidism Type 2 | Mucolipidosis Type IV | Sarcosinemia | Loeys-Dietz Syndrome Type 4 | Down Syndrome | Williams Syndrome | Roberts Syndrome | Thrombosis | Isovaleric Acidemia | Vascular Calcification | Combined Pituitary Hormone Deficiency | Posterior Polar Cataract | Orotic Aciduria | Endometritis | Glaucomatocyclitic Crisis | Neuroleptic Malignant Syndrome | Infertility | Spinocerebellar Ataxia Type 5 | Osteopathia Striata With Cranial Sclerosis | Chondromyxoid Fibroma | Riboflavin Transporter Deficiency Neuronopathy | Primary Aldosteronism | Renal-hepatic-pancreatic Dysplasia | Lateral Meningocele Syndrome | Osteochondroma | Ectrodactyly | Babesiosis | Primary Familial Brain Calcification | Holoprosencephaly | Renal Tubular Dysgenesis | Kaposiform Hemangioendothelioma | Hypermetropia | Splenomegaly | Filariasis | Gliosarcoma | Retinal Coloboma | Spondylosis | Herpes Simplex Dermatitis | MELAS Syndrome | Esophageal Adenocarcinoma | Cardiomyopathy, Peripartum | Common Cold | Sarcoma, Ewing | Medulloblastoma | Choroiditis | Paroxysmal Kinesigenic Dyskinesia | Cleidocranial Dysplasia | Congenital Tufting Enteropathy | Osteochondrosis | Alexander Disease | Chondrodysplasia Punctata | Arthritis | Oligodendroglioma | Delayed Sleep Phase Syndrome | Trigonocephaly | Pleomorphic Xanthoastrocytoma | Goiter | Progressive Myoclonic Epilepsy | Cancer, Prostate | Tay-Sachs Disease | Neurotoxicity | Leber Congenital Amaurosis | Hepatitis B, Chronic | Crisponi Syndrome | Myelodysplasia | Thrombotic Microangiopathy | Dyslexia | Familial Thoracic Aortic Aneurysm | Carey-Fineman-Ziter Syndrome | Hereditary Elliptocytosis | Parkinsonism | Congenital Lipoid Adrenal Hyperplasia | Eosinophilic Asthma | Onchocerciasis | Central Retinal Artery Occlusion | Pfeiffer Syndrome | Autosomal Recessive Spastic Paraplegia Type 35 | McCune-Albright Syndrome | Tic Disorder | Asperger Syndrome | Alagille Syndrome | Cancer, Lung | Granular Corneal Dystrophy | Trachoma | Vitamin D Deficiency | Bronchitis | Benign Familial Neonatal Convulsions | Hyperuricemic Nephropathy, Familial Juvenile | Spinocerebellar Ataxia | Best Macular Dystrophy | Phosphoglycerate Dehydrogenase Deficiency | Ichthyosis, X-linked | Glanzmann Thrombasthenia | 3-hydroxyacyl-CoA Dehydrogenase Deficiency | Sclerocornea | Inflammatory Myofibroblastic Tumor | Liddle Syndrome | Polycystic Kidney, Autosomal Recessive | Platyspondylic Lethal Skeletal Dysplasia, Torrance Type | Craniometaphyseal Dysplasia | Hypervalinemia | Non-small Cell Lung Cancer | Epidermolysis Bullosa Simplex, Localized | Hypokalemia | Gastritis, Atrophic | Autoimmune Disease | Cousin Syndrome | Beta-Propeller Protein-associated Neurodegeneration | Myelomeningocele | Hydrocephalus, Normal Pressure | Congenital Afibrinogenemia