Disease

Hypercalciuria

About the Disease
Hypercalciuria, Absorptive, 2, also known as hypercalciuria, absorptive, susceptibility to, is related to nephrolithiasis, calcium oxalate and nephrolithiasis, and has symptoms including polyuria, lower urinary tract symptoms and urological manifestations. An important gene associated with Hypercalciuria, Absorptive, 2 is ADCY10 (Adenylate Cyclase 10). The drugs Ergocalciferol and Cholecalciferol have been mentioned in the context of this disorder. Affiliated tissues include bone, spinal cord and colon, and related phenotypes are hypercalciuria and calcium oxalate nephrolithiasis

Common Targets
AP2S1 | CASR | CYP24A1 | SLC34A3 | CLDN14 | CLDN19 | ADCY10

疾病靶点研报
Hypercalciuria

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

Other Diseases

Congenital Afibrinogenemia | Hepatorenal Syndrome | Infantile Neuroaxonal Dystrophy | Craniopharyngioma | Toxic Epidermal Necrolysis | Sengers Syndrome | Heroin Dependence | Osteitis | Anorexia Nervosa | Cushing Syndrome | Skin Fragility-woolly Hair Syndrome | Corneal Dystrophy | POEMS Syndrome | Congenital Myopathy | Hypermetropia | Congenital Stromal Corneal Dystrophy | Osteoporosis, Postmenopausal | Nutrition Disorders | Uremic Pruritus | Episodic Ataxia Type 2 | Combined Malonic And Methylmalonic Acidemia | Nicotine Dependence | Retinopathy Of Prematurity | Lassa Fever | Spondyloepiphyseal Dysplasia Tarda, X-linked | Gangliosidosis, GM1 | Porokeratosis | Congenital Dyserythropoietic Anemia Type 1 | Hypereosinophilic Syndrome | Long-chain 3-hydroxyacyl-coenzyme A Dehydrogenase Deficiency | Autoimmune Polyendocrine Syndrome | Premature Ejaculation | Congenital Dyserythropoietic Anemia | Hyperlipidemia | Citrullinemia | Giant Cell Arteritis | Costello Syndrome | Mandibuloacral Dysplasia With Type A Lipodystrophy | Encephalopathy, Glycine | Learning Disability | McLeod Syndrome | Congenital Disorders Of Glycosylation | Chorea | Congenital Dyserythropoietic Anemia Type 4 | Asperger Syndrome | Synovitis | Spondylometaphyseal Dysplasia | Protein C Deficiency | Glycogen Storage Disease | Infantile Spasm | Stargardt Disease | Macular Degeneration | Tyrosinemia | Hemangioma | Multiple Sclerosis | Adenoma, Villous | Chondrodysplasia Punctata | Joubert Syndrome | Galloway-Mowat Syndrome | Glaucoma | Spinocerebellar Ataxia Type 15 | Glutaric Aciduria Type 3 | Chondrodysplasia Punctata 1, X-linked Recessive | Epidermodysplasia Verruciformis | Hemochromatosis Type 2 | Zygomycosis | Keloid | Glioblastoma | Necrobiosis Lipoidica | Autoimmune Interstitial Lung, Joint, And Kidney Disease | Syndactyly | Bleeding Disorder Due To CalDAG-GEFI Deficiency | Rhizomelic Chondrodysplasia Punctata | Pyelonephritis | Congenital Heart Defects | Schwannoma | Bardet-Biedl Syndrome | Narcolepsy | Myosin Storage Myopathy | Nephrosclerosis | Hemochromatosis Type 1 | HANAC Syndrome | Pemphigus Foliaceus | Adenoma, Pituitary | Pyruvate Carboxylase Deficiency Disease | Hepatopulmonary Syndrome | Bipolar Disorder | Mumps | Renal Medullary Carcinoma | Distal Myopathy | Leiomyosarcoma | Alpha-1 Antitrypsin Deficiency | Myopia | Bone Giant Cell Tumor | Poirier-Bienvenu Neurodevelopmental Syndrome | Waldenstrom Macroglobulinemia | Myositis, Focal | Methemoglobinemia Type IV | Achromatopsia | Hyperandrogenemia | Guttate Psoriasis | Pleomorphic Xanthoastrocytoma | Progressive Familial Intrahepatic Cholestasis | Ectodermal Dysplasia | Herpes Simplex Dermatitis | Mitochondrial DNA Depletion Syndrome, Encephalomyopathic Form | IgA Deficiency | Gastritis, Atrophic | Fetal Alcohol Syndrome | Neurodegeneration Due To Cerebral Folate Transport Deficiency | Cyclic Vomiting Syndrome | Hypercholesterolemia, Familial | Intermittent Claudication | Peutz-Jeghers Syndrome | Stroke, Ischemic | Renal-hepatic-pancreatic Dysplasia | Sjogren Syndrome | Cardiofaciocutaneous Syndrome | Colitis, Collagenous | Carcinoid Tumor | Hairy Cell Leukemia | Chronic Leukemia | Combined Pituitary Hormone Deficiency | Greig Cephalopolysyndactyly Syndrome | Norrie Disease | Priapism | Congenital Fiber-type Disproportion Myopathy | Charcot-Marie-Tooth Disease Axonal Type 2N | Seasonal Mood Disorder | Systemic Mastocytosis | Acute Generalized Exanthematous Pustulosis | Duodenal Atresia | Colitis | Metabolic Diseases | Thrombasthenia | Fowler's Syndrome | Glomerulonephritis | Disseminated Intravascular Coagulation | Gynecomastia | Carcinoma, Squamous Cell | Hypertrophy | Lymphopenia | Microvillus Inclusion Disease | Glutathione Synthetase Deficiency | Melanoma | Long QT Syndrome Type 3 | Dementia | Klinefelter Syndrome | Congenital Torticollis | Inflammatory Joint Disease | Histiocytosis | Leprosy | Idiopathic Pulmonary Fibrosis | Chondrodysplasia Punctata 2, X-linked Dominant | Neurodegeneration With Brain Iron Accumulation | Alstrom Syndrome | Alopecia Areata | Conn Syndrome | Metachromatic Leukodystrophy | Peters-plus Syndrome | Primary Hyperoxaluria Type 3 | C3 Glomerulonephritis | Snyder-Robinson Syndrome | Dystonia Musculorum Deformans | Long QT Syndrome Type 1 | McKusick Type Metaphyseal Chondrodysplasia | Cerebral Amyloid Angiopathy | Coma | Botulism | Acute Lung Injury | VEXAS Syndrome | Pregnancy, Ectopic | Delayed Sleep Phase Syndrome | Hartsfield Syndrome | Williams Syndrome | Carney-Stratakis Syndrome | Lymphoma, B-cell | Tic Disorder | Hepatitis D | Diamond-Blackfan Anemia | Bladder Exstrophy | Scleritis | 17-beta-hydroxysteroid Dehydrogenase X Deficiency | Pyoderma Gangrenosum | Cryoglobulinemia | Acne | Skin Papilloma | Acute Myeloid Leukemia | Spasticity | Nanophthalmos | Cenani-Lenz Syndactyly Syndrome | Wolfram Syndrome 2 | Chronic Granulomatous Disease, X-linked | Primary Sclerosing Cholangitis | Ichthyosis Bullosa Of Siemens | Cancer, Brain | Cardiomyopathy, Peripartum | Peeling Skin Syndrome Type B | L-2-Hydroxyglutaric Aciduria | Takotsubo Cardiomyopathy | Renal Hypouricemia | HELLP Syndrome | Hyperglycemia | Restless Legs Syndrome | Mevalonate Kinase Deficiency | Ameloblastic Carcinoma | Neurofibromatosis | Seizures-scoliosis-macrocephaly Syndrome | IMAGe Syndrome | Hereditary Hemorrhagic Telangiectasia | Molybdenum Cofactor Deficiency | Lymphomatoid Granulomatosis | Osmotic Demyelination Syndrome | Retinal Degeneration | 3-hydroxyacyl-CoA Dehydrogenase Deficiency | Familial Hypobetalipoproteinemia | Myoclonic Atonic Epilepsy | Cole-Carpenter Syndrome | Methylmalonic Aciduria And Homocystinuria, CblC Type | Hashimoto Thyroiditis | Hemophilia | Sarcoma, Alveolar Soft Part | Homocystinuria | Hyperphosphatasia With Intellectual Disability Syndrome 4 | Cutaneous Mastocytosis | Sickle Cell Disease | Micro Syndrome | Traboulsi Syndrome | Familial Glucocorticoid Deficiency | Early Infantile Epileptic Encephalopathy 4 | Pigment Dispersion Syndrome | Fucosidosis | Small Lymphocytic Lymphoma | Lupus Erythematosus | Charcot-Marie-Tooth Disease, Type 2C | Chromosome 16p11.2 Deletion Syndrome | Membranous Nephropathy | Calcium Pyrophosphate Deposition Disease | Persistent Fetal Circulation | Renal Oncocytoma | Primary Aldosteronism | Micropenis | Wolcott-Rallison Syndrome | Gout | Primary Pigmented Nodular Adrenocortical Disease | Lymphoma, Follicular | Muscular Dystrophy | Rosacea | Panniculitis | Ectopia Lentis, Isolated, Autosomal Recessive | Epidermolysis Bullosa Dystrophica | Hypertension, Renovascular | Asthma, Exercise-induced | Tyrosine Hydroxylase Deficiency | Warsaw Breakage Syndrome | Congenital Hemolytic Anemia | Congenital Mirror Movements | Uremia | Vertebrobasilar Insufficiency | Chorea-acanthocytosis | Seminoma | Osteosclerosis | Heart Failure | Aceruloplasminemia | Carotid Artery Disease | Ischemia | Charcot-Marie-Tooth Disease Type 4E | Sertoli Cell-only Syndrome | Werner's Syndrome | Pulmonary Capillary Hemangiomatosis | Chediak-Higashi Syndrome | Cockayne Syndrome | Acute Tubular Necrosis | Proximal Symphalangism | Sitosterolemia | Schizencephaly | Retinal Detachment | Pycnodysostosis | Follicular Dendritic Cell Sarcoma | Leukodystrophies | Situs Inversus | Acquired Partial Lipodystrophy | Juvenile Hyaline Fibromatosis | Craniometaphyseal Dysplasia | Fraser Syndrome | Genee-Wiedemann Syndrome | Actinomycetoma | Papilloma | Leukoplakia | Meniere's Disease | Schwannomatosis | Myhre Syndrome | Mannosidase Deficiency Diseases | Iron Overload | Dystonia | Dysthymia | Cancer, Colon | Chordoid Glioma | Graves Disease | Neurofibrosarcoma | Pleurisy | Cutaneous Lupus Erythematosus | Multiple Epiphyseal Dysplasia | Multiple Congenital Anomalies-hypotonia-seizures Syndrome 2 | Cat Eye Syndrome | Triphalangeal Thumb-polysyndactyly Syndrome | Angiosarcoma | Fibrillation, Atrial | Hypertensive Retinopathy | Familial Pheochromocytoma-paraganglioma | Desmosterolosis | Keratitis | Canavan Disease | Progressive External Ophthalmoplegia | Amyotrophic Lateral Sclerosis, Juvenile | Ophthalmoplegia | Holt-Oram Syndrome | Autosomal Recessive Spastic Paraplegia Type 54 | Sarcoidosis | Sclerosteosis 2 | Systemic Lupus Erythematosus | Dysplastic Nevus | Sarcoidosis, Pulmonary | Neuroma | Demyelinating Diseases | Pure Red Cell Aplasia | Anencephaly | Enterocolitis, Necrotizing | Hereditary Spherocytosis | Fibromuscular Dysplasia | Arthritis, Psoriatic | Schizotypal Personality Disorder | Metanephric Adenoma | Leri Pleonosteosis | Iron Metabolism Disorders | Parkinson's Disease | Encephalocele | Renal Dysplasia | Cerebrotendinous Xanthomatosis | Frontometaphyseal Dysplasia | Angina Pectoris | Amyloidosis | Inflammatory Myofibroblastic Tumor | X-linked Myotubular Myopathy | Acrodysostosis | Dystonia-parkinsonism, X-linked | Macrophagic Myofasciitis | Anorectal Malformations | Melanocytic Nevus | Granular Corneal Dystrophy Type 1 | Oculocutaneous Albinism | Jawad Syndrome | Aspergillosis | Pneumonia, Viral | Postpoliomyelitis Syndrome | Pleural Tuberculosis | Pyloric Stenosis, Infantile Hypertrophic | Niemann-Pick Disease, Type A | Motor Neuron Diseases | Intracranial Hypertension | Central Retinal Artery Occlusion | Thymoma, Malignant | Tinea | Birt-Hogg-Dube Syndrome | Presbyopia | Wagner Disease | Splenomegaly | Otosclerosis | Agranulocytosis | Pontocerebellar Hypoplasia Type 7 | Waardenburg Syndrome Type 4 | Astigmatism | Prurigo Nodularis | Adrenoleukodystrophy, X-linked | Hypercalciuria | Angioedema | Pierson Syndrome | Personality Disorders | Vestibular Disease | Pheochromocytoma | Premenstrual Syndrome | Cri-du-chat Syndrome | Sarcoma | Meier-Gorlin Syndrome | Hemangioblastoma | Amish Infantile Epilepsy Syndrome | GAPO Syndrome | Hennekam Lymphangiectasia-lymphedema Syndrome | Lichen Sclerosus | Atelosteogenesis Type 1 | Bursitis | Porphyria Cutanea Tarda | Psoriasis | Epilepsy, Generalized | Pontocerebellar Hypoplasia Type 2 | Porphyria, Variegate | NDH Syndrome | Glycogen Storage Disease Type 1b | Azoospermia | Granular Corneal Dystrophy