Disease

Neurogenic Diabetes Insipidus

About the Disease
Diabetes Insipidus, Neurohypophyseal, also known as neurohypophyseal diabetes insipidus, is related to central diabetes insipidus and pituitary gland disease, and has symptoms including polyuria and polydipsia. An important gene associated with Diabetes Insipidus, Neurohypophyseal is AVP (Arginine Vasopressin), and among its related pathways/superpathways are GPCR downstream signalling and Class A/1 (Rhodopsin-like receptors). The drugs Exenatide and Hydrocortisone have been mentioned in the context of this disorder. Affiliated tissues include pituitary, skin and hypothalamus, and related phenotypes are osteopenia and hypertelorism

Common Targets
AVP | AVPR2

疾病靶点研报
Neurogenic Diabetes Insipidus

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

Other Diseases

Hypotension, Orthostatic | Tricho-hepato-enteric Syndrome | Senior-Loken Syndrome | Congenital Stationary Night Blindness | Low Phospholipid Associated Cholelithiasis | Diabetes Insipidus, Neurogenic | Hodgkin Lymphoma | Diffuse Mesangial Sclerosis | Asphyxia Neonatorum | Kallmann Syndrome | Distal Myopathy 2 | Schizophrenia | Paget's Disease Of The Breast | VACTERL/VATER Association | Ovarian Hyperstimulation Syndrome | Choreoathetosis, Hypothyroidism, And Neonatal Respiratory Distress | Allergic Contact Dermatitis | Cataplexy | MELAS Syndrome | Tendinitis | Peripheral T-cell Lymphoma | Ectodermal Dysplasia | Chiari Malformation Type I | Endocarditis | Leprosy | Metaphyseal Chondrodysplasia, Schmid Type | POEMS Syndrome | Congenital Mirror Movements | Acute Tubular Necrosis | Esotropia | Spondylocarpotarsal Synostosis Syndrome | Meleda Disease | Arthritis | Neutrophilia | Sporadic Inclusion Body Myositis | Congenital Fiber-type Disproportion Myopathy | Usher Syndrome Type III | Retinal Detachment | Cutaneous T-cell Lymphoma | Uremia | Hemophilia | Chronic Granulomatous Disease, X-linked | Fabry's Disease | Ileitis | T-cell Leukemia | LMNA-related Congenital Muscular Dystrophy | Alstrom Syndrome | Corneal Edema | Juvenile Myoclonic Epilepsy | Retinopathy, Diabetic | Cystinosis | Familial Cerebral Amyloid Angiopathy | Joubert Syndrome | Precocious Puberty | Epidermolytic Ichthyosis, Annular | Renal Hypomagnesemia 3 | Joubert Syndrome 2 | Hyperphenylalaninemia | Triple A Syndrome | Down Syndrome | Cerebellofaciodental Syndrome | Mandibuloacral Dysplasia With Type A Lipodystrophy | Dyggve-Melchior-Clausen Disease | Gastritis | Leukemia-lymphoma, Adult T-cell | Ligneous Conjunctivitis | Weill-Marchesani Syndrome | Chronic Kidney Disease | Spasticity | Waardenburg Syndrome Type 2E | Vestibular Disease | Congenital Diaphragmatic Hernia | Periodic Limb Movement Disorder | Stroke, Ischemic | Transient Bullous Dermolysis Of The Newborn | Papillorenal Syndrome | Sturge-Weber Syndrome | Microvillus Inclusion Disease | Stuttering | Amyotrophic Lateral Sclerosis, Juvenile | Myelodysplasia | Hydrolethalus Syndrome | Endometrial Hyperplasia | Presbycusis | Spinocerebellar Ataxia Type 16 | Lennox-Gastaut Syndrome | Myotonic Disorders | Otopalatodigital Syndrome Type 2 | Oculocutaneous Albinism Type 1 | Mitochondrial Disease | Congenital Torticollis | Focal Segmental Glomerulosclerosis | Gastritis, Atrophic | Erectile Dysfunction | Alpha-mannosidosis | Osteogenesis Imperfecta Type V | Epidermal Nevus Syndrome | Porphyria, Variegate | Craniofrontonasal Syndrome | Hidradenitis Suppurativa | Hepatitis B, Chronic | Bainbridge-Ropers Syndrome | Polycystic Kidney, Autosomal Recessive | Klippel-Feil Syndrome | Neonatal Progeroid Syndrome | Craniopharyngioma | Mountain Sickness | Microcephalic Osteodysplastic Primordial Dwarfism, Type I | Gingivitis | Dysgerminoma | Hemorrhage | Lathosterolosis | Glucagonoma | Kashin-Beck Disease | Acromicric Dysplasia | Sarcomatoid Carcinoma Of The Lung | Thrombotic Microangiopathy | Plasma Cell Leukemia | Ganglioglioma | Thanatophoric Dysplasia | Trichuriasis | Mitochondrial DNA Depletion Syndrome, Myopathic Form | Leukemia | Ectopia Lentis, Isolated, Autosomal Recessive | Placenta Previa | Aicardi-Goutieres Syndrome | Basal Cell Nevus Syndrome | 6-pyruvoyl-tetrahydropterin Synthase Deficiency | Tetraplegia | Shprintzen-Goldberg Syndrome | Hyperinsulinemic Hypoglycemia | Hyperparathyroidism | Nemaline Myopathy | Myofibrillar Myopathy | Paronychia | Intestinal Pseudo-obstruction | Cryoglobulinemia | Migraine | Hashimoto Thyroiditis | Blepharophimosis Syndrome | Uremic Pruritus | Blepharoconjunctivitis | Glycogen Storage Disease Type 1 | Neurodegeneration Due To Cerebral Folate Transport Deficiency | Multiple System Atrophy | Poretti-Boltshauser Syndrome | Nicotine Dependence | Measles | Hepatopulmonary Syndrome | Gastroenteritis | Sponastrime Dysplasia | Rhinitis | Infantile Nephropathic Cystinosis | Cold-induced Sweating Syndrome | Hypotrichosis Simplex | Pancytopenia | Agnathia-Otocephaly Complex | Pearson Syndrome | Erdheim-Chester Disease | Polycythemia | Glycogen Storage Disease Type 1a | Rhabdomyosarcoma, Alveolar | Carbohydrate Metabolism Disorders | Heimler Syndrome | Sensorineural Hearing Loss | Glycogen Storage Disease | Corneal Neovascularization | Keratocystic Odontogenic Tumor | CHOPS Syndrome | Vitamin D Deficiency | Cardiac Sarcoidosis | Hypereosinophilic Syndrome | Noonan Syndrome-like Disorder With Loose Anagen Hair | Spitzoid Melanoma | Sclerosteosis 2 | Vogt-Koyanagi-Harada Syndrome | Leri Pleonosteosis | Scleritis | Skin Papilloma | Infantile Spasm | Pityriasis Rubra Pilaris | Encephalopathy, Glycine | Pontocerebellar Hypoplasia Type 7 | Congenital Afibrinogenemia | Methylmalonic Acidemia | Crigler-Najjar Syndrome | Carcinoma, Squamous Cell | Dubin-Johnson Syndrome | Meningioma, Benign | Purpura | Inflammatory Linear Verrucous Epidermal Nevus | Robinow Syndrome | Congenital Disorders Of Glycosylation | Encephalopathy | Usher Syndrome Type II | Muscle Wasting | Cyclic Vomiting Syndrome | Microcephalic Osteodysplastic Primordial Dwarfism, Type II | Craniolenticulosutural Dysplasia | Hypoglycemia | Protein C Deficiency | Thrombasthenia | Hereditary Neuropathy With Liability To Pressure Palsies | Hemoglobinopathies | Axenfeld-Rieger Syndrome | Glycogen Storage Disease Type 6 | Motor Neuron Diseases | Acrocallosal Syndrome | Hyperinsulinism-hyperammonemia Syndrome | Charcot-Marie-Tooth Disease Type 4 | Microtia | Spinocerebellar Ataxia Type 2 | Sarcoidosis | Congenital Tufting Enteropathy | Diastrophic Dysplasia | Hartsfield Syndrome | Retinal Dystrophy, Early-onset Severe | Phosphoenolpyruvate Carboxykinase Deficiency, Cytosolic | Macular Degeneration | Stromal Corneal Dystrophy | Arts Syndrome | Charcot-Marie-Tooth Disease, Type 6 | DOCK8 Immunodeficiency Syndrome | X-linked Charcot-Marie-Tooth Disease | Micropenis | CREST Syndrome | Obesity, Morbid | Alpha-1 Antitrypsin Deficiency | Bare Lymphocyte Syndrome | Microphthalmia | Paternal Uniparental Disomy Of Chromosome 14 | Papilledema | Non-proliferative Diabetic Retinopathy | Encephalopathy, Hepatic | Treacher Collins Syndrome | Werner's Syndrome | Bronchiectasis | Dyslexia | Mood Disorder | Hereditary Mixed Polyposis Syndrome | Cryptococcal Meningitis | Renal Tubular Acidosis | Platyspondylic Lethal Skeletal Dysplasia, Torrance Type | Bicuspid Aortic Valve | Multiple Congenital Anomalies-hypotonia-seizures Syndrome 2 | Tularemia | Tuberculosis | Hypohidrotic Ectodermal Dysplasia | Walker-Warburg Syndrome | Cranial Nerve Disease | Kabuki Syndrome | Neurofibromatosis Type 2 | Hyperparathyroidism-jaw Tumor Syndrome | Arthritis, Reactive | Wolfram Syndrome | Brachial Plexus Neuropathy | Anal Fissure | Sickle Cell Anemia | Schizotypal Personality Disorder | Antiphospholipid Syndrome | Toxoplasmosis | Peeling Skin Syndrome Type B | Lentigo | Dental Caries | Congenital Aniridia | Goiter | Blastoma, Pleuropulmonary | Congenital Myasthenic Syndrome | Polycystic Liver | Hypothalamic Obesity | Phenylketonuria | Porphyria | Sick Sinus Syndrome | Carotid Artery Disease | Canavan Disease | Neurogenic Bladder | Spinocerebellar Ataxia Type 17 | Delirium | Hereditary Hemorrhagic Telangiectasia | Glomerulonephritis, Membranoproliferative | Hemochromatosis | Coma | Xeroderma Pigmentosum Variant Type | Galloway-Mowat Syndrome | Glutathione Synthetase Deficiency | Phosphoglycerate Dehydrogenase Deficiency | Epidermolysis Bullosa Simplex With Mottled Pigmentation | Pneumonia, Viral | Sleep Disorder | Tardive Dyskinesia | Amyotrophic Lateral Sclerosis-parkinsonism-dementia Complex | Dengue Shock Syndrome | Light Chain Amyloidosis | Danon Disease | Localized Scleroderma | Mycosis Fungoides | Keratopathy | Pure Red Cell Aplasia | Thromboembolism | Adenoma, Pituitary | Keloid | Iron Metabolism Disorders | Varicocele | Spinocerebellar Ataxia Type 10 | Bleeding Disorder Due To CalDAG-GEFI Deficiency | Spondylo-ocular Syndrome | Seborrheic Dermatitis | Syphilis | Exfoliative Dermatitis | Osteoporosis | Celiac Disease | Pulmonary Sclerosing Hemangioma | Conjunctivitis | Adenomatoid Tumor | Androgen Insensitivity | Enhanced S-cone Syndrome | Ectrodactyly | Charcot-Marie-Tooth Disease Type 4E | Oligoastrocytoma | Sensory Ataxic Neuropathy, Dysarthria, And Ophthalmoparesis | Lassa Fever | Coffin-Lowry Syndrome | Iron Deficiency Anemia | Herpes Simplex Dermatitis | Huntington's Disease-like 2 | Periodontitis | Li-Fraumeni Syndrome | Paroxysmal Kinesigenic Dyskinesia | Pompe Disease | Peutz-Jeghers Syndrome | Stomatitis | Keratitis | Dysferlinopathy | TARP Syndrome | Hypertriglyceridemia | Binge Eating Disorder | VEXAS Syndrome | HELLP Syndrome | Dysequilibrium Syndrome | Hartnup Disease | Meningococcal Infections | Loeys-Dietz Syndrome | GAPO Syndrome | CDKL5 Deficiency Disorder | Ganglioneuroma | Bursitis | Ataxia-hypogonadism-choroidal Dystrophy Syndrome | Coronary Heart Disease | Optic Neuritis | Retinal Telangiectasia | Dermatitis | Oculodentodigital Dysplasia | Polymicrogyria | Birt-Hogg-Dube Syndrome | Spina Bifida | Nail-Patella Syndrome | Carcinoma, Small Cell | Open-angle Glaucoma | Overactive Bladder | Cervical Dystonia | Pneumothorax | Encephalocele | Graft-versus-host Disease | Goldenhar Syndrome | Dermatitis Herpetiformis | Pyoderma Gangrenosum | CEDNIK Syndrome | Graves Disease | Hepatitis, Autoimmune | Creatine Deficiency Syndrome | Mitochondrial Cytopathy | Acrodermatitis | Persistent Fetal Circulation | Astigmatism | Familial Hyperaldosteronism | Pyruvate Kinase Deficiency | Parkinsonism | Chronic Granulomatous Disease | Familial Hemiplegic Migraine | Multisystemic Smooth Muscle Dysfunction Syndrome | Alkaptonuria | Intermittent Explosive Disorder | Carpenter Syndrome | Molybdenum Cofactor Deficiency | Seizures | Hepatitis D | Aldosterone Deficiency | Scapuloperoneal Myopathy, X-linked Dominant | Autonomic Nervous System Disorders | Fatty Aldehyde Dehydrogenase Deficiency | Multiple Mitochondrial Dysfunctions Syndrome Type 1 | Thymoma, Malignant | Cysticercosis | Polyarteritis Nodosa | Hereditary Coproporphyria | Pseudomyxoma Peritonei | Paracoccidioidomycosis | Bone Marrow Necrosis | Tinea | Speech Disorders