Interstitial Lung Diseases

About the Disease
Interstitial Lung Disease, also known as ild, is related to interstitial pneumonitis, desquamative, familial and rheumatoid arthritis interstitial lung disease, and has symptoms including shortness of breath, coughing and hemoptysis. An important gene associated with Interstitial Lung Disease is INPP5E (Inositol Polyphosphate-5-Phosphatase E), and among its related pathways/superpathways are Innate Immune System and Metabolism of proteins. The drugs Prednisone and Cyclophosphamide have been mentioned in the context of this disorder. Affiliated tissues include lung, bone marrow and skeletal muscle, and related phenotypes are homeostasis/metabolism and neoplasm

Common Targets
P2RX1 | HLA-A | LPAR1 | ALOX5AP | GLIS3 | TGFBR1 | D21S2088E | G3480 | FARSB | XDH | G7422 | LINC01239 | NKX2-1 | G7015 | MMP12 | Tyrosine Kinase (nonspecified subtype) | IVD | AQP4 | CTLA4 | NF-kappaB (NFkB) | SFTPA1 | CCN2 | HER (erbB) (nonspecified subtype) | SERPINE1 | SSH2 | NOX4 | CHIT1 | PDGFRA | PDE5A | CD86 | TOLLIP | KIT | ITGA3 | FARSA | Interleukin-12 (IL-12) | IFNG | DSP | SFTPC | DDR1 | STAT4 | NOX3 | LIPC | TGFB1 | Transforming growth factor beta (nonspecified subtype) | RTEL1 | HLA-DQB1 | Triacylglycerol Lipase (TG Lipase) (nonspecified subtype) | ABL1 | CD80 | PON1 | NADPH Oxidase Complex | Nitric oxide synthase (NOS) (nonspecified subtype) | IL6R | LOXL2 | HLA-DPB1 | MIR3667HG | Integrin alphavbeta6 receptor | SFTPA2 | SFTPD | HLA-C | LINC01276 | AGTR2 | G6774 | PDGFRB | Cytochrome P450 Enzymes (nonspecified subtype) | CSF1R | MARS1 | NADPH Oxidase (nonspecified subtype) | HLA-DRB1 | CCL18 | MEP1A | NOX1 | GRIN2B | MEP1B | LIPE | DAGLA | ELANE | G5243 | G4780 | SLC25A48 | CCSER1 | PDE4D | PORCN | LTC4S | HLA-B | TGFB3 | GRN | ABCA3 | Integrin alphavbeta8 Receptor | CMA1 | RPA3 | TSHZ2 | FGFR3 | LIPG | G7124 | TYK2 | TNFRSF13B | HABP4 | ENPP2 | SPP1 | G3569 | CACNA1H | Integrin alphavbeta3 (vitronectin) receptor | KDR | ZC3H12A | PDE4B | UMAD1 | HLA-DQA1 | BRD4 | G9429 | FLT4 | FGFR1 | FLT1 | TSNARE1 | PREP | SNAI3-AS1 | IKBKB | VDR | ZNF664-RFLNA | VAMP1 | PARN | ALDH2 | BCR | G1950 | Folate Receptor (nonspecified subtype)

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

Other Diseases

Beckwith-Wiedemann Syndrome | Gastroenteritis | Hereditary Spherocytosis | Scleroderma | Amelanotic Melanoma | Meningococcal Meningitis | Carpenter Syndrome | Smith-Lemli-Opitz Syndrome | L-2-Hydroxyglutaric Aciduria | Chondrodysplasia Punctata | Currarino Syndrome | Diabetic Macular Edema | Silicosis | Osteomalacia | Zimmermann-Laband Syndrome | Myoclonic Atonic Epilepsy | Neurofibromatosis-Noonan Syndrome | Corneal Edema | Cholelithiasis | Infertility | Sarcosinemia | Retinoblastoma | Myasthenia Gravis | Niemann-Pick Disease, Type C | Pouchitis | Diabetic Encephalopathy | Precocious Puberty | Coronary Artery Disease | Coffin-Lowry Syndrome | Goiter | Emery-Dreifuss Muscular Dystrophy | Kaposi Sarcoma | Sulfite Oxidase Deficiency | Inflammatory Joint Disease | Choroideremia | Clouston Hidrotic Ectodermal Dysplasia | Addison Disease | Pheochromocytoma | Erectile Dysfunction | Congenital Dysfibrinogenemia | Fibrosis | Narcolepsy | Polycystic Liver | Hepatitis C, Chronic | Macular Corneal Dystrophy | Hyperlipidemia | Acute Myeloid Leukemia | Polycystic Kidney, Autosomal Dominant | Fraser Syndrome | Carcinoma, Squamous Cell | Hypophosphatasia | Osmotic Demyelination Syndrome | Myositis, Focal | Multicystic Renal Dysplasia | Pierpont Syndrome | Malignant Fibrous Histiocytoma | Peeling Skin Syndrome Type B | Behcet's Disease | Asthma, Exercise-induced | Myopia | Optic Neuropathy, Anterior Ischemic | Bipolar Disorder | Facioscapulohumeral Muscular Dystrophy | Pulverulent Zonular Cataract | Dentinogenesis Imperfecta | Vascular Calcification | Brachydactyly | Astrocytoma | Obesity | Epilepsy Of Infancy With Migrating Focal Seizures | Botulism | Bloom Syndrome | Neutropenia | Fuchs Dystrophy | Microphthalmia | Agranulocytosis | Pelvic Inflammatory Disease | Focal Cortical Dysplasia Type 2 | Melnick-Needles Syndrome | Amelogenesis Imperfecta | Craniofacial Dysostosis | Spinocerebellar Ataxia Type 14 | Frontotemporal Dementia With Amyotrophic Lateral Sclerosis | Hemorrhagic Disorders | Tyrosinemia | Endometriosis | Steel Syndrome | Ichthyosis Hystrix, Curth-Macklin Type | Leukoencephalopathy, Progressive Multifocal | Pneumonia, Mycoplasma | Pemphigoid | Hypohidrotic Ectodermal Dysplasia, X-linked | Infantile Nephropathic Cystinosis | Astigmatism | Cranioectodermal Dysplasia | Acute Lung Injury | Congenital Generalized Lipodystrophy | Multiple Hamartoma Syndrome | Pneumonia, Bacterial | Kleine-Levin Syndrome | Charcot-Marie-Tooth Disease, Type 1A | Spinocerebellar Ataxia Type 17 | Multiple Sclerosis, Secondary Progressive | Paget's Disease Of The Breast | Dysequilibrium Syndrome | Amish Infantile Epilepsy Syndrome | Communication Disorders | Chiari Malformation Type I | Myoclonic Epilepsy With Ragged Red Fibers | Primary Lateral Sclerosis | Essential Fructosuria | Niemann-Pick Disease, Type B | Macrodactyly | Kernicterus | Huntington's Disease | Polycystic Kidney, Autosomal Recessive | Thin Basement Membrane Disease | Cleidocranial Dysplasia | Congenital Torticollis | Ehlers-Danlos Syndrome | Thyrotoxic Periodic Paralysis | Cholangiocarcinoma | Familial Exudative Vitreoretinopathy | Idiopathic Pulmonary Fibrosis | Hereditary Hemorrhagic Telangiectasia | Hypercalcemia | Cherubism | Microcephalic Primordial Dwarfism | Cutis Laxa | Pseudohypoparathyroidism Type 1B | Silver-Russell Syndrome | Enlarged Vestibular Aqueduct | Gyrate Atrophy Of The Choroid And Retina | Amenorrhea | Congenital Bilateral Absence Of Vas Deferens | Renal-hepatic-pancreatic Dysplasia | Aplasia Cutis Congenita | Carbonic Anhydrase VA Deficiency | Vasculitis | Hypogonadism | Neurocutaneous Syndromes | Lymphoma, B-cell | Schuurs-Hoeijmakers Syndrome | Wiskott-Aldrich Syndrome | Oculocutaneous Albinism Type 4 | Orotic Aciduria | Congenital Dyserythropoietic Anemia | Congenital Disorders Of Glycosylation | Leishmaniasis, Visceral | Thanatophoric Dysplasia Type 1 | Lesch-Nyhan Syndrome | Epidermolysis Bullosa Simplex With Mottled Pigmentation | Diverticulitis | Recurrent Respiratory Papillomatosis | Mitochondrial DNA Depletion Syndrome 13 | Cranial Nerve Disease | Arthritis, Psoriatic | Hyperoxaluria | Superficial Spreading Melanoma | Cardiomyopathy, Hypertrophic | Cancer, Bladder | Ehlers-Danlos Syndrome With Progressive Kyphoscoliosis, Myopathy, And Hearing Loss | Epithelial-myoepithelial Carcinoma | Congenital Mirror Movements | Primary Erythromelalgia | Pyruvate Dehydrogenase Deficiency | Spondylocostal Dysostosis | Multiple Sclerosis, Relapsing-remitting | Paternal Uniparental Disomy Of Chromosome 14 | Cancer, Brain | Angiosarcoma Of The Breast | Vitreoretinopathy, Proliferative | HANAC Syndrome | 5-oxoprolinase Deficiency | Arterial Tortuosity Syndrome | Ectopia Lentis, Isolated, Autosomal Recessive | Hyperphosphatasia With Intellectual Disability Syndrome 4 | Neurocutaneous Melanocytosis | Trichomegaly | Purpura | Tonsillitis | Platyspondylic Lethal Skeletal Dysplasia, Torrance Type | Nephrotic Syndrome | Wieacker-Wolff Syndrome | Pemphigus Vulgaris | Esophageal Carcinoma | Gilbert Syndrome | Arthritis | Absence Epilepsy | Hereditary Multiple Exostoses | Celiac Disease | TARP Syndrome | 3-hydroxy-3-methylglutaryl-CoA Synthase Deficiency | Seizures | Charcot-Marie-Tooth Disease, Type 2C | Sarcoma, Endometrial Stromal | Blepharo-cheilo-odontic Syndrome | Congenital Disorders Of Glycosylation Type II | Familial Digital Arthropathy-brachydactyly | POEMS Syndrome | CDKL5 Deficiency Disorder | Arthritis, Gouty | Apert Syndrome | Hepatic Adenomatosis | Interstitial Lung Diseases | Asplenia | Retinal Dystrophy, Early-onset Severe | Acromesomelic Dysplasia | Membranous Nephropathy | Cavitary Optic Disc Anomalies | Lymphoma, Mantle Cell | Progressive Familial Intrahepatic Cholestasis | Bronchitis | Poirier-Bienvenu Neurodevelopmental Syndrome | Lactose Intolerance | Pantothenate Kinase-associated Neurodegeneration | Spinocerebellar Ataxia Type 38 | Lipoma | Megaloblastic Anemia | Pleurisy | Pyoderma Gangrenosum | Oligoastrocytoma | Colitis, Microscopic | Neurodegeneration With Brain Iron Accumulation | Primary Aldosteronism | Sporadic Hemiplegic Migraine | Analgesia | Oculocutaneous Albinism Type 2 | Allergic Contact Dermatitis | Woodhouse-Sakati Syndrome | Mucolipidosis Type IV | Schizophrenia | Extramammary Paget's Disease | Hyperkeratosis | Lipid Storage Diseases | Coloboma | Porphyria Cutanea Tarda | Leishmaniasis, Cutaneous | Spinal Cord Diseases | Oligodendroglioma | Sandhoff Disease | Myoclonus | Ghosal Syndrome | Pineoblastoma | Hyperandrogenemia | Waldenstrom Macroglobulinemia | Spitzoid Melanoma | Menkes Disease | Eclampsia | Dwarfism | PHARC Syndrome | Early Infantile Epileptic Encephalopathy | VEXAS Syndrome | Muscular Dystrophy | 3-methylcrotonyl-CoA Carboxylase Deficiency | Sturge-Weber Syndrome | Holt-Oram Syndrome | Gray Platelet Syndrome | Asphyxia Neonatorum | Porokeratosis | Anosmia, Congenital | Kohlschutter-Tonz Syndrome | Myocarditis | Stuttering | Temporal Lobe Epilepsy | Hypolipoproteinemia | Hypotrichosis | Hyperthyroidism | Adenylosuccinate Lyase Deficiency | Headache | Transcobalamin Deficiency | Localized Scleroderma | Oral Lichen Planus | Gastric Atrophy | Trichothiodystrophy | Cryptorchidism | Pure Autonomic Failure | Gastrointestinal Disorders | Triphalangeal Thumb-polysyndactyly Syndrome | Motion Sickness | Congenital Lipoid Adrenal Hyperplasia | 3-hydroxyacyl-CoA Dehydrogenase Deficiency | Chordoma | Tibial Muscular Dystrophy | Pseudo-pseudohypoparathyroidism | Speech Disorders | Pseudohypoaldosteronism | Thyroid Dyshormonogenesis | Spinocerebellar Ataxia Type 15 | Palmoplantar Keratoderma | Meningioma, Benign | Adenocarcinoma | Congenital Dyserythropoietic Anemia Type 1 | Bardet-Biedl Syndrome | Focal Segmental Glomerulosclerosis | Scapuloperoneal Spinal Muscular Atrophy | Spinal Muscular Atrophy Type 2 | Polyneuropathy | Maternally Inherited Diabetes And Deafness | Long QT Syndrome Type 2 | Liver Diseases | Thrombotic Microangiopathy | Mitochondrial Disease | Asperger Syndrome | Majeed Syndrome | Seizures-scoliosis-macrocephaly Syndrome | Acute Tubular Necrosis | Skin Fragility-woolly Hair Syndrome | Chondrosarcoma | HELLP Syndrome | Sarcoidosis | Carbamoyl Phosphate Synthetase I Deficiency | Klinefelter Syndrome | Methylmalonic Acidemia | Leukoplakia | Rubeosis Iridis | Urolithiasis | Neuromyelitis Optica | Chondrodysplasia Punctata 1, X-linked Recessive | Meleda Disease | Weill-Marchesani Syndrome | Tuberculous Meningitis | Giant Axonal Neuropathy | Choreoathetosis, Hypothyroidism, And Neonatal Respiratory Distress | Leber Congenital Amaurosis | DNA Ligase IV Deficiency | Sarcoidosis, Pulmonary | Myelofibrosis | Rhabdomyosarcoma, Embryonal | Papillorenal Syndrome | Usher Syndrome Type IIC | Pleomorphic Xanthoastrocytoma | Sick Sinus Syndrome | Fanconi Syndrome | Congenital Heart Block | Primary Hyperoxaluria Type 1 | Hypokalemia | Epidermolysis Bullosa Simplex | Keratosis | Acquired Partial Lipodystrophy | Snyder-Robinson Syndrome | Hepatopulmonary Syndrome | Spasticity | Werner's Syndrome | Lamellar Ichthyosis | Metatropic Dysplasia | Pigment Dispersion Syndrome | Sialidosis Type I | Carcinoma, Transitional Cell | WAGR Syndrome | Megalencephaly | Von Hippel-Lindau Disease | Hyperekplexia | Waardenburg Syndrome Type 1 | Glaucoma, Congenital | NGLY1 Deficiency | Hyperlipidemia Type V | Obsessive-compulsive Disorder | Familial Partial Lipodystrophy | Castleman Disease | Mitochondrial Myopathy | Pure Red Cell Aplasia | Lewy Body Dementia | 3-methylglutaconic Aciduria Type I | Hyperbilirubinemia | Pterygium | Aicardi-Goutieres Syndrome | Malignant Peripheral Nerve Sheath Tumor | Trichotillomania | Hypertrophic Osteoarthropathy, Primary, Autosomal Recessive 1 | Thrombophlebitis | Inflammatory Linear Verrucous Epidermal Nevus | Hidradenitis | Carcinoma, Small Cell | Vascular Cognitive Impairment | Acne | Anxiety Disorders | Acanthosis Nigricans | Adenoma, Villous | Osteosclerosis | Congenital Tufting Enteropathy | Bone Giant Cell Tumor | Cerebral Cavernous Malformations | Insulin Resistance | Aldosteronism | Polymicrogyria | Erythema Nodosum | Combined Malonic And Methylmalonic Acidemia | 3C Syndrome | Bleeding Disorder Due To CalDAG-GEFI Deficiency | Schwannoma | Von Willebrand Disease | Colitis | Epidermolysis Bullosa Simplex, Generalized | Lattice Corneal Dystrophy | Spondyloepiphyseal Dysplasia Tarda, X-linked | Early Infantile Epileptic Encephalopathy 1 | Chorioretinitis | Liebenberg Syndrome | Apraxia