Disease

Interstitial Nephritis

About the Disease
Interstitial Nephritis, also known as nephritis, interstitial, is related to interstitial nephritis, karyomegalic and nephronophthisis 16. An important gene associated with Interstitial Nephritis is MT-TF (Mitochondrially Encoded TRNA-Phe (UUU/C)), and among its related pathways/superpathways are Ciliopathies and Joubert syndrome. The drugs Sodium citrate and Potassium citrate have been mentioned in the context of this disorder. Affiliated tissues include kidney, t cells and bone marrow, and related phenotypes are homeostasis/metabolism and renal/urinary system

Common Targets
HLA-DRB1 | HLA-DQA1 | FAN1 | IGHE | IL10 | UMOD | AIRE | HLA-DQB1

疾病靶点研报
Interstitial Nephritis

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

Other Diseases

Aldosteronism | Agnathia-Otocephaly Complex | Thyroid Hormone Resistance | Pituitary Stalk Interruption Syndrome | Hyperandrogenemia | Infantile Refsum Disease | Silicosis | Pseudohermaphroditism | Renpenning Syndrome | Jacobsen Syndrome | Perry Syndrome | Wiedemann-Steiner Syndrome | Hepatorenal Syndrome | Nasodigitoacoustic Syndrome | Miyoshi Myopathy | Traboulsi Syndrome | Cerebral Amyloid Angiopathy | Hyperinsulinism-hyperammonemia Syndrome | Myelofibrosis | Onchocerciasis | Inflammatory Linear Verrucous Epidermal Nevus | Progressive Myoclonic Epilepsy | Borjeson-Forssman-Lehmann Syndrome | Schizotypal Personality Disorder | Cabezas Syndrome | Facioscapulohumeral Muscular Dystrophy Type 1 | Mesial Temporal Lobe Epilepsy With Hippocampal Sclerosis | 3C Syndrome | Diabetes Insipidus, Nephrogenic | Pleurisy | Hemophilia | Metachondromatosis | Hypotonia-cystinuria Syndrome | Agoraphobia | Osteogenesis Imperfecta Type VI | Kaposiform Hemangioendothelioma | Tremor | Fanconi Syndrome | Glanzmann Thrombasthenia | Goldenhar Syndrome | Vasculitis | Tietze Syndrome | Hepatopulmonary Syndrome | Bardet-Biedl Syndrome | Heart Failure | Osteopathia Striata With Cranial Sclerosis | Ameloblastoma | Amyloidosis | Acrodermatitis Enteropathica | Non-Hodgkin Lymphoma | Gigantism | Dyslexia | Keratosis | Cerebellofaciodental Syndrome | Medium-chain Acyl-CoA Dehydrogenase Deficiency | Diabetes Type 1 | Chronic Kidney Disease | Osteoporosis-pseudoglioma Syndrome | Cryptorchidism | Williams Syndrome | Greenberg Dysplasia | LMNA-related Congenital Muscular Dystrophy | Kindler Syndrome | Neuromuscular Disorders | Bipolar Disorder | Juvenile Myoclonic Epilepsy | TARP Syndrome | Myasthenia | Fibrosis | Benign Familial Pemphigus | Hypertension, Essential | Sclerosing Cholangitis | Scabies | L-2-Hydroxyglutaric Aciduria | Meier-Gorlin Syndrome | Dermatitis | Cirrhosis | Smith-Lemli-Opitz Syndrome | Brenner Tumor | Cystitis, Interstitial | Retinopathy, Diabetic | Uveitis | Nephropathy | Pontocerebellar Hypoplasia | Carpenter Syndrome | Pituitary Disorders | Spinal Muscular Atrophy Type 3 | Hepatitis | Acute Generalized Exanthematous Pustulosis | Riboflavin Transporter Deficiency Neuronopathy | Echinococcosis | Asphyxia Neonatorum | Pleomorphic Xanthoastrocytoma | Tularemia | Encephalopathy, Glycine | Pneumococcal Meningitis | Hyperparathyroidism, Primary | Hemolytic Anemia | Craniopharyngioma | Bruck Syndrome | Short-chain Acyl-CoA Dehydrogenase Deficiency | Vitelliform Macular Dystrophy | Pancreatitis, Chronic | Spondylo-megaepiphyseal-metaphyseal Dysplasia | Myeloid Leukemia | Dengue Hemorrhagic Fever | Meningioma, Benign | Acute Kidney Injury | Oligodendroglioma | Coronary Restenosis | Crimean-Congo Hemorrhagic Fever | Cohen Syndrome | Malnutrition | Blomstrand Osteochondrodysplasia | Ghosal Syndrome | Non-bullous Congenital Ichthyosiform Erythroderma | Anterior Segment Dysgenesis | Primary Lateral Sclerosis | Schizoaffective Disorder | Acne | Autonomic Neuropathy | Superficial Spreading Melanoma | Pulmonary Capillary Hemangiomatosis | Loeys-Dietz Syndrome Type 4 | Muckle-Wells Syndrome | Congenital Myasthenic Syndrome | Guillain-Barre Syndrome | Hepatitis B, Chronic | Hemangioblastoma | Leukoencephalopathy, Progressive Multifocal | Multiple Hamartoma Syndrome | Anuria | Leri-Weill Dyschondrosteosis | Exfoliative Dermatitis | Diabetes | VACTERL Association | Lissencephaly 2 | Periodontitis | Parkinson's Disease | Hypothyroidism | Hypoglycemia | Diabetic Neuropathy | Inflammatory Myopathy | NGLY1 Deficiency | Lymphopenia | Hennekam Lymphangiectasia-lymphedema Syndrome | Clouston Hidrotic Ectodermal Dysplasia | Lymphoma, B-cell | N-acetylglutamate Synthase Deficiency | Otitis Media | Aplasia Cutis Congenita | Carney Triad | Endocarditis | Choroiditis | Microcephaly, Seizures, And Developmental Delay | Haim-Munk Syndrome | Brachydactyly | Nijmegen Breakage Syndrome | Corneal Dystrophy And Perceptive Deafness | Arthropathy | Hyperammonemia | Ameloblastic Carcinoma | Bursitis | Pitt-Hopkins Syndrome | Hypocalcemia | Systemic Mastocytosis | Otosclerosis | Intermittent Explosive Disorder | Erythema Multiforme | Intellectual Disability, Autosomal Dominant 5 | Saul-Wilson Syndrome | Anosmia, Congenital | Vertebrobasilar Insufficiency | Dysferlinopathy | Spondyloepiphyseal Dysplasia Tarda, X-linked | Eosinophilic Asthma | Tricho-hepato-enteric Syndrome | Varicocele | Colitis | Oligoastrocytoma | Avellino Corneal Dystrophy | Corneal Dystrophy | Amyotrophic Lateral Sclerosis, Juvenile | Familial Pheochromocytoma-paraganglioma | Bartter Syndrome | Crisponi Syndrome | Hyperparathyroidism-jaw Tumor Syndrome | Carotid Artery Disease | Maple Syrup Urine Disease | Encephalopathy, Ethylmalonic | Leukemia-lymphoma, Adult T-cell | Persistent Fetal Circulation | Epilepsy, Generalized | Hypogonadism | Familial Mediterranean Fever | Spinal Muscular Atrophy | Spinocerebellar Ataxia Type 3 | Glycogen Storage Disease Type 5 | Lymphoma, Follicular | Spondylocostal Dysostosis | Lymphedema | Lattice Corneal Dystrophy Type 1 | Absence Epilepsy | Atopy | Congenital Generalized Lipodystrophy | 3-M Syndrome | Peeling Skin Syndrome Type B | Impulse Control Disorder | Glomerulonephritis | Chronic Myeloid Leukemia | Panniculitis | Pyruvate Carboxylase Deficiency Disease | Ichthyosis Bullosa Of Siemens | Lymphedema-distichiasis Syndrome | Tyrosine Hydroxylase Deficiency | Brooke-Spiegler Syndrome | Familial Hyperaldosteronism | Dermatitis Herpetiformis | Astigmatism | Patent Ductus Arteriosus | Pure Red Cell Aplasia | Idiopathic Pulmonary Fibrosis | Carney-Stratakis Syndrome | Cluster Headache | Raine Syndrome | Influenza | Vitreoretinopathy, Proliferative | Tetraplegia | Hodgkin Lymphoma | Alagille Syndrome | WAGR Syndrome | Ectrodactyly | Congenital Disorders Of Glycosylation | T-cell Prolymphocytic Leukemia | Hemorrhagic Disorders | Microcephalic Osteodysplastic Primordial Dwarfism, Type II | Apraxia | Hypertrophic Osteoarthropathy, Primary, Autosomal Recessive 2 | Carbonic Anhydrase VA Deficiency | Multiple Sclerosis | Spinal Cord Diseases | Corneal Dystrophies, Hereditary | Waldenstrom Macroglobulinemia | Osteonecrosis | Congenital Hypofibrinogenemia | Mitochondrial Encephalomyopathy | Spinocerebellar Ataxia Type 8 | Cousin Syndrome | Overactive Bladder | Emery-Dreifuss Muscular Dystrophy | Avian Influenza | IgA Deficiency | Charcot-Marie-Tooth Disease, Type 2C | Spondylometaphyseal Dysplasia | Cramp Fasciculation Syndrome | Meningitis | Ehlers-Danlos Syndrome With Progressive Kyphoscoliosis, Myopathy, And Hearing Loss | Sandhoff Disease | Generalized Epilepsy With Febrile Seizures Plus | Hoyeraal-Hreidarsson Syndrome | Cutaneous Angiosarcoma | Fatty Aldehyde Dehydrogenase Deficiency | Hypermethioninemia | Tinea | Keratopathy | Supravalvular Aortic Stenosis | Nephritis, Interstitial | Treacher Collins Syndrome | Dystonia | Aspartylglycosaminuria | Gerodermia Osteodysplastica | Uveitis, Anterior | Autosomal Recessive Congenital Ichthyosis | Arthritis, Reactive | Neurocutaneous Melanocytosis | Intracerebral Hemorrhage | Lymphangiomatosis | Postpartum Depression | Aneurysm, Thoracic Aortic | Feingold Syndrome | Basal Ganglia Disease, Biotin-responsive | Melanocytic Nevus | Graft-versus-host Disease | Oculocutaneous Albinism Type 1 | Goiter | Farber Disease | Cancer, Kidney | Hyperprolactinemia | Colorectal Adenoma | Anorexia Nervosa | Diffuse Palmoplantar Keratoderma | Hypertension | Apparent Mineralocorticoid Excess Syndrome | CREST Syndrome | Gangliosidosis, GM1 | Reticular Dysgenesis | Leber Congenital Amaurosis | Growth Hormone Excess | Herpes Simplex Dermatitis | Cataract | Lipid Metabolism Disorders | Sweet Syndrome | Asthma | Sezary Syndrome | Spondylocarpotarsal Synostosis Syndrome | Spinocerebellar Ataxia | Cysticercosis | Glycogen Storage Disease Type 9 | Wolff-Parkinson-White Syndrome | Aphasia | Sensorineural Hearing Loss | Carcinoma, Signet Ring Cell | Fontaine Progeroid Syndrome | Temporal Lobe Epilepsy | Tracheal Disorders | Histiocytosis | Presbyopia | Congenital Muscular Dystrophy | Chronic Thromboembolic Pulmonary Hypertension | Neurofibromatosis-Noonan Syndrome | Biotinidase Deficiency | 3-methylglutaconic Aciduria Type I | Spondyloarthritis | Porphyria | Urethritis | Spinocerebellar Ataxia Type 23 | Gangliosidosis | Binge Eating Disorder | Congenital Torticollis | Odonto-onycho-dermal Dysplasia | Hypersomnia | Chronic Neutrophilic Leukemia | Glutaric Aciduria Type 1 | 3-methylglutaconic Aciduria Type IV | Carcinoid Tumor | Charcot-Marie-Tooth Disease, Type 2 | Kawasaki Disease | Polycystic Liver | Hereditary Spherocytosis | Hereditary Inclusion Body Myopathy | Charcot-Marie-Tooth Disease Type 4D | Pseudoachondroplasia | Niemann-Pick Disease, Type A | Bloom Syndrome | Very Long-chain Acyl-CoA Dehydrogenase Deficiency | Pseudohypoparathyroidism Type 2 | Dementia | Open-angle Glaucoma | Hyperoxaluria | Polymyalgia Rheumatica | Menkes Disease | Schistosomiasis | Botulism | Scleroderma, Diffuse | Conjunctivitis | Neurofibroma | Pseudohypoaldosteronism | Choreoathetosis, Hypothyroidism, And Neonatal Respiratory Distress | Hypereosinophilic Syndrome | Heterotaxy | Cerebral Cavernous Malformations | Birt-Hogg-Dube Syndrome | Asperger Syndrome | Diastrophic Dysplasia | Hyperkalemic Periodic Paralysis | Cannabis Abuse | Psoriasis | Glaucoma, Congenital | Desmosterolosis | Diabetes Gestational | Choriocarcinoma | Sarcomatoid Carcinoma Of The Lung | Sarcoma, Alveolar Soft Part | Epidermolysis Bullosa Simplex | Craniometaphyseal Dysplasia | Hemorrhage | Hypohidrotic Ectodermal Dysplasia | Coronary Artery Disease | Keratosis, Seborrheic | Cockayne Syndrome | Poirier-Bienvenu Neurodevelopmental Syndrome | Familial Episodic Pain Syndrome | Neurogenic Bladder | Schizophrenia | Carcinoid Syndrome | Sotos Syndrome | Stuttering | MIRAGE Syndrome | Osteopetrosis | Neonatal Progeroid Syndrome | Anxiety Disorders | Osteomyelitis | Osteogenesis Imperfecta Type III | Woodhouse-Sakati Syndrome | Stargardt Disease | Cole-Carpenter Syndrome | Papillon-Lefevre Syndrome | Peutz-Jeghers Syndrome | Actinomycetoma | Chronic Enteropathy Associated With SLCO2A1 Gene