Disease

Kidney Stones

About the Disease
Nephrolithiasis, also known as kidney stones, is related to nephrolithiasis, calcium oxalate and nephrolithiasis/osteoporosis, hypophosphatemic, 1, and has symptoms including renal pain An important gene associated with Nephrolithiasis is SLC25A25 (Solute Carrier Family 25 Member 25), and among its related pathways/superpathways are Transport of inorganic cations/anions and amino acids/oligopeptides and Disorders of transmembrane transporters. The drugs Mirabegron and Ropivacaine have been mentioned in the context of this disorder. Affiliated tissues include kidney, bone and prostate, and related phenotypes are renal/urinary system and homeostasis/metabolism

Common Targets
CASR | G9429 | G4318 | VDR | SLC22A12 | SCNN1B | HIBADH | CYP24A1 | GCKR | SLC13A5 | SLC26A6 | PRODH | WDR72 | HOGA1 | FGF23 | RGS14 | PTH | LDHA | SLC34A1 | UMOD | PTH1R | CLDN4 | SLC34A3 | BCAS3 | CLDN14 | PDILT | CALCR | GIPC1 | CLDN18 | CLDN11 | TRPV5 | SPP1 | CLDN17 | DGKH | GNAZ | ALPL | POU2AF1 | MGP | HAO1 | UGT1A10 | G5243 | SLC7A9 | SLC26A1 | CASR | UGT1A8 | G23411 | SLC22A12 | UGT1A7 | NR1I2 | SLC26A3 | SLC4A1 | CYP24A1 | ATP6V1B1 | DYTN | ADAM23 | UGT1A6 | SLC26A6 | CYP3A5 | UGT1A4 | UGT1A9 | NRXN1 | FGF23 | UGT1A5 | RGS14 | UGT1A1 | POU4F2 | SLCO1B1 | CLDN2 | OXGR1 | CLDN16 | SLC34A1 | CARMIL1 | SLC34A3 | CMAHP | MINDY4 | NHERF1 | SPP1 | DGKH | UGT1A3 | APRT | ADCY10 | SLC3A1

疾病靶点研报
Kidney Stones

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

Other Diseases

Fragile X Syndrome | Omenn Syndrome | Pearson Syndrome | Gaze Palsy, Familial Horizontal, With Progressive Scoliosis, 2 | Hepatitis, Alcoholic | Gastric Atrophy | Congenital Myopathy | Spinocerebellar Ataxia Type 38 | Gitelman Syndrome | Rubinstein-Taybi Syndrome | Giant Cell Arteritis | Anorchia | Spondyloperipheral Dysplasia | Congenital Bilateral Absence Of Vas Deferens | Blue Nevus | Paraganglioma, Carotid Body | NDH Syndrome | Isobutyryl-CoA Dehydrogenase Deficiency | HIBCH Deficiency | Olmsted Syndrome | B-cell Prolymphocytic Leukemia | Progressive Osseous Heteroplasia | Benign Familial Pemphigus | Oligodendroglioma | Liebenberg Syndrome | Polymyositis | Bronchiectasis | Adult Polyglucosan Body Disease | Bardet-Biedl Syndrome | Androgen Insensitivity | Congenital Heart Block | Enterocolitis, Necrotizing | Lymphoproliferative Disease, X-linked | Renal Hypomagnesemia 3 | Noonan Syndrome-like Disorder With Loose Anagen Hair | Uveitis, Anterior | Skin Papilloma | Fraser Syndrome | Hoyeraal-Hreidarsson Syndrome | Deafness, Dystonia, And Cerebral Hypomyelination | Cholecystitis | 3-hydroxy-3-methylglutaric Aciduria | Hyperlipidemia, Familial Combined | Basal Cell Nevus Syndrome | ADNP Syndrome | Stargardt Disease | Astrocytoma, Anaplastic | Polycythemia Vera | Retinal Degeneration | Niemann-Pick Disease, Type C | HANAC Syndrome | Sorsby Fundus Dystrophy | Ornithine Transcarbamylase Deficiency | Cardiomyopathy, Hypertrophic | Avian Influenza | Diabetic Macular Edema | Lattice Corneal Dystrophy | Charcot-Marie-Tooth Disease Type 4 | Vertebrobasilar Insufficiency | Osteogenesis Imperfecta Type II | Cerebellofaciodental Syndrome | Stevens-Johnson Syndrome | Ataxia-hypogonadism-choroidal Dystrophy Syndrome | Lactose Intolerance | Spinocerebellar Ataxia Type 5 | Panniculitis | Scabies | Lattice Corneal Dystrophy Type 1 | Uveitis | Contact Dermatitis | Myelomeningocele | Hypertension, Pulmonary | Dengue Shock Syndrome | Wilson's Disease | Monilethrix | X-linked Charcot-Marie-Tooth Disease | REM Sleep Behavior Disorder | Schwannomatosis | Nicotine Addiction | Prolidase Deficiency | 3-M Syndrome | Lentigo | Lymphopenia | Ligneous Conjunctivitis | Fetal Akinesia Deformation Sequence | Neuromyotonia | Diverticulitis | Endocarditis | Lennox-Gastaut Syndrome | Low Tension Glaucoma | Thromboembolism | Cornelia De Lange Syndrome | Intestinal Pseudo-obstruction | Alopecia Totalis | Borjeson-Forssman-Lehmann Syndrome | Celiac Disease | Basan Syndrome | Asplenia | Microcephaly | T-cell Leukemia | Nephrotic Syndrome | Cardiofaciocutaneous Syndrome | Hereditary Hemorrhagic Telangiectasia Type 2 | Nutrition Disorders | Spondylo-ocular Syndrome | Takotsubo Cardiomyopathy | Obsessive-compulsive Disorder | Hepatorenal Syndrome | Hereditary Hemorrhagic Telangiectasia | Common Cold | Glomerulonephritis, Membranoproliferative | Chordoma | Progressive Myoclonic Epilepsy | Spinocerebellar Ataxia Type 27 | Congenital Generalized Lipodystrophy | Chronic Periodontitis | Meningococcal Meningitis | Nager Acrofacial Dysostosis | Hypertriglyceridemia | Raynaud Phenomenon | Pancreatitis | Glioblastoma | Netherton Syndrome | Cancer, Brain | Schistosomiasis Mansoni | Phosphoenolpyruvate Carboxykinase Deficiency, Cytosolic | Hypopituitarism | Iron Overload | Auriculocondylar Syndrome | Trichuriasis | Small Lymphocytic Lymphoma | Spinocerebellar Ataxia Type 23 | Glycogen Storage Disease Type 1a | Cryptorchidism | Neurogenic Bladder | Dementia, Vascular | Rheumatic Heart Disease | Pneumococcal Meningitis | Colitis, Lymphocytic | Smith-Lemli-Opitz Syndrome | Acute Generalized Exanthematous Pustulosis | Pneumothorax | Pleomorphic Xanthoastrocytoma | Hemochromatosis | Neuroblastoma | Carney Triad | Hypospadias | Heart Septal Defects | LMNA-related Congenital Muscular Dystrophy | Vitamin D Deficiency | Chronic Myelomonocytic Leukemia | Histoplasmosis | Dowling-Degos Disease | Ovarian Sex Cord-stromal Tumor | Cholera | Tibial Muscular Dystrophy | Achromatopsia | Renal Hypouricemia | Veno-occlusive Disease | Hypobetalipoproteinemias | Agnathia-Otocephaly Complex | Ulcerative Colitis | Oculocutaneous Albinism Type 1 | Pancytopenia | Gallstones | Retinal Dystrophy | Lipoma | Vitiligo | Retinal Coloboma | Schuurs-Hoeijmakers Syndrome | Pancreatitis, Chronic | Werner's Syndrome | Cellulitis | Hyperinsulinism-hyperammonemia Syndrome | Bloom Syndrome | Osteogenesis Imperfecta Type IV | Peeling Skin Syndrome Type B | Craniosynostosis | Birt-Hogg-Dube Syndrome | Vulvovaginitis | Spinocerebellar Ataxia Type 28 | Congenital Stromal Corneal Dystrophy | Dental Caries | Non-Hodgkin Lymphoma | Guttate Psoriasis | Spinocerebellar Ataxia Type 21 | Marfan Syndrome | Hepatoblastoma | Glutathione Synthetase Deficiency | Aplasia Cutis Congenita | Sturge-Weber Syndrome | Tetraplegia | Lamellar Ichthyosis | Juvenile Xanthogranuloma | Chondrosarcoma | Mitochondrial DNA Depletion Syndrome, Hepatocerebral Form | Hemophagocytic Lymphohistiocytosis | Mitochondrial Disease | Leiomyoma | Spasticity | Oral Lichen Planus | Thrombosis | Cholesteryl Ester Storage Disease | Vogt-Koyanagi-Harada Syndrome | Melanoma | Mohr-Tranebjaerg Syndrome | Hereditary Inclusion Body Myopathy | Mesothelioma, Malignant | Erysipelas | Polyomavirus Nephropathy | Sengers Syndrome | Hyperparathyroidism, Primary | Von Hippel-Lindau Disease | Maple Syrup Urine Disease | Maternally Inherited Diabetes And Deafness | Glycogen Storage Disease Type 0, Muscle | Triple A Syndrome | Endometriosis | Metaphyseal Chondrodysplasia, Schmid Type | Leukemia-lymphoma, Adult T-cell | Dyggve-Melchior-Clausen Disease | Primary Erythromelalgia | Pituitary Dwarfism | Hepatitis B, Chronic | Disseminated Intravascular Coagulation | Camurati-Engelmann Disease | Skin Fragility-woolly Hair Syndrome | Pulmonary Veno-occlusive Disease | Hypertelorism | Keratoconus | Alexander Disease | Creatine Deficiency Syndrome | Necrotizing Autoimmune Myopathy | Gastroenteritis, Eosinophilic | Dysmorphophobia | Pure Red Cell Aplasia | Oligospermia | Vitelliform Macular Dystrophy | Fahr Disease | Specific Granule Deficiency | Depression | Splenomegaly | Hemophilia | Chiari Malformation Type I | Central Retinal Artery Occlusion | Neurofibrosarcoma | Colon Adenoma | Tendinitis | Chronic Granulomatous Disease | Parapsoriasis | Primary Cutaneous Amyloidosis | Senior-Loken Syndrome | Nephrocalcinosis | Vaginitis | Graft-versus-host Disease | Ganglioglioma | Hyperuricemic Nephropathy, Familial Juvenile | Lichen Planus | Sandhoff Disease | Adenosine Deaminase Deficiency | Persistent Truncus Arteriosus | Spinocerebellar Ataxia | Hemimegalencephaly | Fetal Alcohol Syndrome | Prediabetes | Pulmonary Capillary Hemangiomatosis | Epidermolysis Bullosa Dystrophica | Gangliosidosis | Lyme Disease | KBG Syndrome | Thrombophlebitis | Hypertensive Nephropathy | Angiosarcoma | Periodontitis | Rhizomelic Chondrodysplasia Punctata | Premenstrual Syndrome | Aphasia | Nemaline Myopathy 10 | Muscular Dystrophy | Persistent Fetal Circulation | Liddle Syndrome | Acromicric Dysplasia | Vasculitis | Lymphoma, Mantle Cell | Keratoacanthoma | Bietti Crystalline Dystrophy | Pyruvate Dehydrogenase Deficiency | Alazami Syndrome | Neurofibromatosis Type 1 | Noonan Syndrome | Angiomyolipoma | Charcot-Marie-Tooth Disease, Type 2A | Granular Corneal Dystrophy Type 1 | Autoimmune Polyendocrine Syndrome | Juvenile Myoclonic Epilepsy | Chronic Leukemia | Gerstmann-Straussler-Scheinker Syndrome | Keratopathy | Familial Glucocorticoid Deficiency | Spitzoid Melanoma | Multiple Hamartoma Syndrome | Alopecia Areata | Non-bullous Congenital Ichthyosiform Erythroderma | Rash | Renal Medullary Carcinoma | Leiomyosarcoma | Hypopigmentation | Keratitis-ichthyosis-deafness Syndrome | Uremic Pruritus | Bartsocas-Papas Syndrome | Herpes Simplex Dermatitis | AIDS Dementia Complex | Polydactyly | Nicotine Dependence | Niemann-Pick Disease, Type A | Blepharophimosis Syndrome | Esophageal Motility Disorders | Presbyopia | Osteosarcoma | Hyperphenylalaninemia | Coronary Heart Disease | Yellow Fever | Myoclonus | Renal Failure | Acrocallosal Syndrome | Acral Lentiginous Melanoma | Hamartoma | Ollier Disease | Neurodevelopmental Disorder With Central Hypotonia And Dysmorphic Facies | Hypotrichosis, Congenital, With Juvenile Macular Dystrophy | Hypophosphatemic Rickets With Hypercalciuria, Hereditary | Centronuclear Myopathy | Pontocerebellar Hypoplasia | Hyperbilirubinemia | Vitreoretinopathy, Proliferative | Trismus-pseudocamptodactyly Syndrome | Hartsfield Syndrome | Sponastrime Dysplasia | Progressive External Ophthalmoplegia | Cancer, Skin | Juvenile Myelomonocytic Leukemia | Gestational Trophoblastic Disease | Ganglioneuroma | Arthritis, Psoriatic | Mosaic Variegated Aneuploidy Syndrome 2 | Motor Neuron Diseases | VACTERL/VATER Association | Hypoproteinemia, Hypercatabolic | Papilledema | Intestinal Hypomagnesemia 1 | Cholangiocarcinoma | Pure Autonomic Failure | Pericarditis | Agoraphobia | Papulopustular Rosacea | Hypereosinophilic Syndrome | POEMS Syndrome | Cerebrovascular Disorders | Sarcomatoid Carcinoma Of The Lung | Congenital Aniridia | Usher Syndrome Type IIC | Galactosialidosis | Opisthorchiasis | Mucolipidosis Type III | Fukuyama Congenital Muscular Dystrophy | Postpoliomyelitis Syndrome | Hyperacusis | Motion Sickness | Hepatitis, Chronic | Retinitis | Macular Corneal Dystrophy | Dentinogenesis Imperfecta | Lymphangioma | Sialoadenitis | Carcinoma, Small Cell | Klinefelter Syndrome | Leishmaniasis, Cutaneous | Hypogonadism | Blue Rubber Bleb Nevus Syndrome | Asphyxia Neonatorum | Peroxisomal Disorder | Benign Familial Infantile Seizures | Amyotrophic Lateral Sclerosis-parkinsonism-dementia Complex | Pigment Dispersion Syndrome | Neurodermatitis | Isovaleric Acidemia | Syncope | Hypophosphatemic Rickets, Autosomal Recessive, 1 | Ichthyosis, X-linked | Stroke, Hemorrhagic | Blastoma, Pleuropulmonary | Epicondylitis | Metanephric Adenoma | Osteogenesis Imperfecta Type I | Glycogen Storage Disease Type 9 | Double Outlet Right Ventricle | Rhinitis | Paroxysmal Nocturnal Hemoglobinuria | Chromosome 17q21.31 Deletion Syndrome | Protein C Deficiency