Hypersensitivity Pneumonitis

About the Disease
Extrinsic Allergic Alveolitis, also known as hypersensitivity pneumonitis, is related to farmer's lung and tropical spastic paraparesis, and has symptoms including hemoptysis An important gene associated with Extrinsic Allergic Alveolitis is SFTPD (Surfactant Protein D), and among its related pathways/superpathways are Signal Transduction and ERK Signaling. The drugs Chlorhexidine and Ethanol have been mentioned in the context of this disorder. Affiliated tissues include lung, skeletal muscle and bone marrow, and related phenotypes are homeostasis/metabolism and immune system

Common Targets
ZKSCAN1 | LTA | HLA-DRB1 | FAM13A | G7124 | TOLLIP | DSP | MMP2 | AOC1 | SMAD3 | MAOB | HLA-DQB1 | MMP1 | AOC3 | ATP11A

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

Other Diseases

Vitiligo | Spinocerebellar Ataxia Type 28 | Rickets | Carcinoma, Merkel Cell | Reflex Epilepsy | Spinocerebellar Ataxia Type 1 | Trichothiodystrophy | 3-hydroxy-3-methylglutaryl-CoA Synthase Deficiency | Pyelonephritis | Hemorrhoids | Spondyloarthritis | Impulse Control Disorder | Ectodermal Dysplasia | Fundus Albipunctatus | REM Sleep Behavior Disorder | Relapsing Polychondritis | Autonomic Nervous System Disorders | Leukodystrophies | Spinocerebellar Ataxia Type 31 | Craniofacial Dysostosis | Charcot-Marie-Tooth Disease, Type 2A | Primary Torsion Dystonia | Vascular Cognitive Impairment | Hypothyroidism | Carcinoid Syndrome | Hepatitis D | Sjogren Syndrome | Cardiomyopathy, Dilated, 1L | Congenital Dyserythropoietic Anemia Type 4 | Endophthalmitis | Schnyder Crystalline Corneal Dystrophy | Neutrophilia | Unverricht-Lundborg Syndrome | Chitayat Syndrome | Otitis Externa | Chloridorrhea, Congenital | Lymphoproliferative Disorders | Neuronal Ceroid Lipofuscinosis | Carbonic Anhydrase VA Deficiency | Ovarian Hyperstimulation Syndrome | Rhinitis | Low Phospholipid Associated Cholelithiasis | Peeling Skin Syndrome Type B | Parkinson's Disease | Giant Axonal Neuropathy | Colitis, Microscopic | Muscle Wasting | Myelitis | Exostoses | Hemolytic Uremic Syndrome | Oligoastrocytoma | Diabetes Gestational | Polycystic Kidney, Autosomal Dominant | Hepatoblastoma | Antisynthetase Syndrome | Arthritis, Psoriatic | Diffuse Palmoplantar Keratoderma | Multiple Myeloma | Pseudohypoparathyroidism Type 1C | Glaucoma | Metabolic Diseases | Spondylo-megaepiphyseal-metaphyseal Dysplasia | Early Infantile Epileptic Encephalopathy 1 | Pulmonary Alveolar Proteinosis | Charcot-Marie-Tooth Disease Type 4B1 | Hypomyelination With Atrophy Of Basal Ganglia And Cerebellum | Osteogenesis Imperfecta Type II | Platyspondylic Lethal Skeletal Dysplasia, Torrance Type | Wolcott-Rallison Syndrome | Blastomycosis | Erythema Nodosum | Proximal Symphalangism | Hypotrichosis Simplex | Primary Hyperoxaluria | Gilbert Syndrome | Mumps | Jacobsen Syndrome | Spitz Nevus | Malignant Peripheral Nerve Sheath Tumor | Neutropenia | Xeroderma Pigmentosum | Neuroleptic Malignant Syndrome | Spinocerebellar Ataxia Type 38 | Dengue Shock Syndrome | Vertebrobasilar Insufficiency | Brachial Plexus Neuropathy | Wolfram Syndrome 2 | Spinocerebellar Ataxia Type 2 | Leukemia | Sensory Neuropathy | Spinocerebellar Ataxia Type 13 | Hypodontia | Hepatitis, Alcoholic | Progressive Familial Intrahepatic Cholestasis | Ellis-Van Creveld Syndrome | Glycogen Storage Disease Type 6 | Cholestasis, Intrahepatic | Pierre Robin Syndrome | Progressive Familial Intrahepatic Cholestasis Type 2 | Aneurysm, Thoracic Aortic | Congenital Dyserythropoietic Anemia Type 1 | Charcot-Marie-Tooth Disease, Type 1A | Photosensitivity | Lichen Planus | Turner's Syndrome | Corneal Dystrophies, Hereditary | Hyperparathyroidism-jaw Tumor Syndrome | Schistosomiasis | Cranioectodermal Dysplasia | Tularemia | Leber Hereditary Optic Neuropathy | Neurofibromatosis | Lymphoma, B-cell | Primary Sclerosing Cholangitis | Pycnodysostosis | Abetalipoproteinemia | Arterial Tortuosity Syndrome | Myelodysplasia | Sclerosteosis | Centronuclear Myopathy | Diverticulitis | Micro Syndrome | WAGR Syndrome | Schnitzler Syndrome | L-2-Hydroxyglutaric Aciduria | Gerodermia Osteodysplastica | Aneurysm, Abdominal Aortic | Addison Disease | Smoldering Myeloma | Lissencephaly 2 | Joubert Syndrome 2 | Torticollis | Hyperuricemic Nephropathy, Familial Juvenile | Brooke-Spiegler Syndrome | Dermatomyositis | Angina Pectoris | Otitis Media | Acanthosis Nigricans | Hemolytic Uremic Syndrome, Atypical | Progressive Encephalopathy-optic Atrophy Syndrome | Pulmonary Capillary Hemangiomatosis | Fatty Aldehyde Dehydrogenase Deficiency | Primary Carnitine Deficiency | Gastritis, Atrophic | Hypermethioninemia | Iron Deficiency Anemia | Sturge-Weber Syndrome | Neonatal Progeroid Syndrome | Erythema Multiforme | Schizencephaly | Syndactyly | Congenital Central Hypoventilation Syndrome | Cold-induced Sweating Syndrome | Glycogen Storage Disease | Cancer, Skin | Gnathodiaphyseal Dysplasia | Giant Cell Arteritis | Megaloblastic Anemia | Choreoathetosis, Hypothyroidism, And Neonatal Respiratory Distress | Camptocormia | Ollier Disease | Congenital Hereditary Endothelial Dystrophy Type II | Hereditary Hemorrhagic Telangiectasia Type 2 | Encephalitis | Huntington's Disease-like 2 | NGLY1 Deficiency | Vestibular Disease | Craniosynostosis | Ganglioneuroma | Crigler-Najjar Syndrome | Marfan Syndrome | Influenza | Tonsillitis | Macular Corneal Dystrophy Type 1 | Polyomavirus Nephropathy | Astigmatism | Dyggve-Melchior-Clausen Disease | Nutrition Disorders | Porokeratosis | Ventricular Septal Defect | C3 Glomerulonephritis | Mitochondrial DNA Depletion Syndrome 13 | Hydrocephalus | Esophageal Adenocarcinoma | Adenomyosis | Pituitary Disorders | Renal Oncocytoma | Depression | Familial Hemiplegic Migraine | Hypokalemic Periodic Paralysis | Congenital Bile Acid Synthesis Defect | Frontotemporal Dementia With Amyotrophic Lateral Sclerosis | Weill-Marchesani Syndrome | Pregnancy, Ectopic | Renal Tubular Dysgenesis | Hypoparathyroidism | Benign Recurrent Intrahepatic Cholestasis 1 | Polyarteritis Nodosa | Immunoproliferative Disorders | Fibromuscular Dysplasia | Sarcomatoid Carcinoma Of The Lung | Viral Meningitis | Pancreatitis, Chronic | Oculocutaneous Albinism | Glutathione Synthetase Deficiency | Pyruvate Dehydrogenase Deficiency | Glycogen Storage Disease Type 3 | Oligoasthenoteratozoospermia | Eczema | Sweet Syndrome | Hypereosinophilic Syndrome | Coronary Artery Disease | Polycythemia | Acral Lentiginous Melanoma | Chromosome 16p11.2 Deletion Syndrome | Histiocytosis | Swine Influenza | Pontocerebellar Hypoplasia | Partington Syndrome | Cantu Syndrome | Learning Disability | Nasodigitoacoustic Syndrome | Iron Metabolism Disorders | Migraine | Hypotonia-cystinuria Syndrome | Epidermolysis Bullosa Acquisita | Myotonia | Cherubism | Mucolipidosis Type IV | Dysgerminoma | Li-Fraumeni Syndrome | Peeling Skin Syndrome, Acral Type | Mitochondrial DNA Depletion Syndrome, Encephalomyopathic Form | AIDS | Schamberg Disease | Aarskog-Scott Syndrome | Long-chain 3-hydroxyacyl-coenzyme A Dehydrogenase Deficiency | Renal Hypomagnesemia 3 | Astrocytoma | Conn Syndrome | Choroiditis | Dementia | Blepharospasm | Acute Motor Axonal Neuropathy | Perivascular Epithelioid Cell Tumor | Lymphoma | Muscular Dystrophy | Familial Isolated Hyperparathyroidism | Chylothorax, Congenital | Delayed Sleep Phase Syndrome | Progressive Osseous Heteroplasia | Congenital Mirror Movements | Osteochondroma | Hepatopulmonary Syndrome | DRESS Syndrome | Dent Disease | Hypohidrotic Ectodermal Dysplasia, X-linked | Antley-Bixler Syndrome | Nephrocalcinosis | Pseudohypoparathyroidism Type 2 | Diabetes Type 1 | Posterior Polar Cataract | Robinow Syndrome | Chorioretinitis | Van Der Knaap Disease | Wagner Disease | Seasonal Mood Disorder | Cardiac Arrest | Basal Ganglia Cerebrovascular Disease | Wolfram Syndrome | Adenosine Deaminase 2 Deficiency | Membranous Nephropathy | Familial Dysautonomia | Epilepsy Of Infancy With Migrating Focal Seizures | Meleda Disease | Ocular Hypertension | Beta-Propeller Protein-associated Neurodegeneration | Common Variable Immunodeficiency | Erectile Dysfunction | Juvenile Myelomonocytic Leukemia | Corneal Dystrophy | Holt-Oram Syndrome | Glycogen Storage Disease Type 1b | Stroke, Hemorrhagic | Peripheral Neuropathy | Hyperbilirubinemia | Arteriosclerosis | Orthostatic Intolerance | Gallstones | Focal Cortical Dysplasia Type 2 | Splenomegaly | Cholelithiasis | Epithelial-myoepithelial Carcinoma | Barrett Esophagus | Micropenis | Gyrate Atrophy Of The Choroid And Retina | Sporadic Hemiplegic Migraine | CHOPS Syndrome | Tinea Versicolor | Currarino Syndrome | Heart Failure | Tic Disorder | Lentigo | Transthyretin-related Amyloidosis | Succinic Semialdehyde Dehydrogenase Deficiency | Pneumonia, Mycoplasma | Avellino Corneal Dystrophy | Oral Lichen Planus | Very Long-chain Acyl-CoA Dehydrogenase Deficiency | Klinefelter Syndrome | Neurocutaneous Syndromes | VACTERL Association | Myelomeningocele | Usher Syndrome Type III | Acute Generalized Exanthematous Pustulosis | Coffin-Lowry Syndrome | Spinocerebellar Ataxia Type 40 | Sleep Apnea | Kaposiform Hemangioendothelioma | Pfeiffer Syndrome | Spastic Paraplegia Type 7 | Pontocerebellar Hypoplasia Type 2 | Adrenoleukodystrophy, X-linked | Nephrotic Syndrome Type 1 | Familial Episodic Pain Syndrome | Facioscapulohumeral Muscular Dystrophy Type 2 | Osteonecrosis | Anorexia Nervosa | Fraser Syndrome | Headache | Waardenburg Syndrome Type 4A | Insulin Resistance | Osteoporosis-pseudoglioma Syndrome | Charcot-Marie-Tooth Disease, Type 2C | Gout | Pneumothorax | Bethlem Myopathy | Echinococcosis | Meier-Gorlin Syndrome | Hypolipoproteinemia | Colitis, Lymphocytic | Schindler Disease | Pachyonychia Congenita | Esophagitis | Cornelia De Lange Syndrome | Acne Vulgaris | Nager Acrofacial Dysostosis | Obsessive-compulsive Disorder | Best Macular Dystrophy | Diastrophic Dysplasia | Craniometaphyseal Dysplasia | Loeys-Dietz Syndrome Type 4 | Chiari Malformation Type I | Motion Sickness | Sponastrime Dysplasia | Microvillus Inclusion Disease | Myositis, Focal | Schizotypal Personality Disorder | Thalassemia | Calcium Pyrophosphate Deposition Disease | Persistent Hyperplastic Primary Vitreous | Melanoma | Tylosis With Esophageal Cancer | Papilledema | Congenital Muscular Dystrophy | Genee-Wiedemann Syndrome | Retinopathy, Diabetic | Palmoplantar Keratoderma | Congenital Nystagmus | Osteosclerosis | Mucolipidosis | Neurodevelopmental Disorder With Central Hypotonia And Dysmorphic Facies | Keratoconus | Mesial Temporal Lobe Epilepsy With Hippocampal Sclerosis | Contact Dermatitis | Niemann-Pick Disease, Type C | Epidermolysis Bullosa Simplex, Generalized | Temtamy Preaxial Brachydactyly Syndrome | Dystonia-parkinsonism, X-linked | Coronary Restenosis | Tangier Disease | Multifocal Motor Neuropathy | Whipple's Disease | Speech Disorders | Uveitis | Paronychia | Adenocarcinoma | Exfoliative Dermatitis | Skin Carcinoma | Asthma | Arrhythmogenic Right Ventricular Cardiomyopathy | Traboulsi Syndrome | Leukocyte Adhesion Deficiency | Wolff-Parkinson-White Syndrome | Fragile X Syndrome | Zollinger-Ellison Syndrome | Beare-Stevenson Syndrome | Ovarian Sex Cord-stromal Tumor | Carcinoma, Squamous Cell | Polycystic Ovary Syndrome