Pituitary Dwarfism

About the Disease
Hypopituitarism, also known as pituitary insufficiency, is related to combined pituitary hormone deficiencies, genetic forms and culler-jones syndrome. An important gene associated with Hypopituitarism is PROP1 (PROP Paired-Like Homeobox 1), and among its related pathways/superpathways are Signal Transduction and G-Beta Gamma Signaling. The drugs Epitestosterone and Diclofenac have been mentioned in the context of this disorder. Affiliated tissues include pituitary, thyroid and brain, and related phenotypes are no effect and no effect

Common Targets
HESX1 | GH1

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

Other Diseases

Autonomic Neuropathy | Cholecystitis | Retinoschisis | Diabetes Insipidus, Nephrogenic | Retinitis | Cirrhosis | Ocular Surface Squamous Neoplasia | Down Syndrome | Hemorrhagic Disorders | Primary Erythromelalgia | Zellweger Syndrome | Hyperostosis | Polyneuropathy | Aceruloplasminemia | Protein S Deficiency | X-linked Myotubular Myopathy | Distal Spinal Muscular Atrophy | Lactose Intolerance | Blepharo-cheilo-odontic Syndrome | Amelanotic Melanoma | Peyronie's Disease | Spinocerebellar Ataxia Type 3 | Cavitary Optic Disc Anomalies | LRBA Deficiency | Anorexia Nervosa | Liddle Syndrome | Hereditary Spastic Paraplegia | Hypertrophic Osteoarthropathy, Primary, Autosomal Recessive 2 | Microcephalic Osteodysplastic Primordial Dwarfism, Type II | Hereditary Hemorrhagic Telangiectasia | Glycogen Storage Disease Type 1 | Harlequin Ichthyosis | Spinal Muscular Atrophy With Progressive Myoclonic Epilepsy | AIDS | Tonsillitis | Aldosterone Deficiency | Prolymphocytic Leukemia | Carey-Fineman-Ziter Syndrome | Focal Segmental Glomerulosclerosis | Pneumothorax | Xeroderma Pigmentosum Variant Type | Silver-Russell Syndrome | Cold Agglutinin Disease | Arthritis, Reactive | Sporadic Inclusion Body Myositis | Netherton Syndrome | Colitis, Lymphocytic | X-linked Charcot-Marie-Tooth Disease | Scapuloperoneal Spinal Muscular Atrophy | Multiple Myeloma | Apert Syndrome | Purpura | Coronary Artery Disease | Trachoma | Carbohydrate Metabolism Disorders | Fragile X Syndrome | Tinea | Lennox-Gastaut Syndrome | Hypotonia-cystinuria Syndrome | Fowler's Syndrome | Prolactinoma | Osteosarcoma | Batten Disease | Multisystemic Smooth Muscle Dysfunction Syndrome | Long QT Syndrome Type 3 | Amyotrophic Lateral Sclerosis | Adenomatoid Tumor | Ichthyosis | Giant Axonal Neuropathy | Diabetes Type 1 | Anorchia | Anuria | Babesiosis | Mesothelioma, Malignant | Conjunctivitis, Allergic | Herpes Simplex Dermatitis | Tyrosinemia Type 1 | Nicotine Dependence | Extramammary Paget's Disease | Jaundice, Obstructive | Encephalopathy | Smith-Kingsmore Syndrome | Greig Cephalopolysyndactyly Syndrome | Gastroschisis | Neonatal Progeroid Syndrome | Weill-Marchesani Syndrome | Alagille Syndrome | Kearns-Sayre Syndrome | Familial Glucocorticoid Deficiency | Schizotypal Personality Disorder | Oligospermia | Glycogen Storage Disease Type 5 | Rash | Esophageal Motility Disorders | Cerebellofaciodental Syndrome | Hyperthyroidism | Palmoplantar Keratoderma | Mitochondrial Cytopathy | Optic Neuropathy | Wagner Disease | Sulfite Oxidase Deficiency | Oculodentodigital Dysplasia | Periventricular Nodular Heterotopia | Thrombasthenia | Microcephaly | Neuronal Ceroid Lipofuscinosis | HANAC Syndrome | Angioedema | Cholangiocarcinoma | Leri-Weill Dyschondrosteosis | Poretti-Boltshauser Syndrome | Salla Disease | Diastrophic Dysplasia | McCune-Albright Syndrome | Dermatomyositis | Azoospermia | Hodgkin Lymphoma | Lymphomatoid Granulomatosis | Hypodontia | Cousin Syndrome | Pitt-Hopkins Syndrome | Vaginitis | Diabetes Insipidus | Cardiofaciocutaneous Syndrome | Osteopathia Striata With Cranial Sclerosis | Basan Syndrome | Myelomeningocele | Loeys-Dietz Syndrome Type 4 | Photosensitivity | Dysferlinopathy | Birt-Hogg-Dube Syndrome | Juvenile Myoclonic Epilepsy | Echinococcosis | Cysticercosis | Hepatitis, Alcoholic | Acrodermatitis | Angioedema, Acquired | Ichthyosis Bullosa Of Siemens | Congenital Torticollis | Angiomyolipoma | MELAS Syndrome | Craniometaphyseal Dysplasia | Neurofibroma, Plexiform | Spondylocostal Dysostosis | Asperger Syndrome | Aldosterone Synthase Deficiency | Craniofacial Dysostosis | Cataplexy | Interstitial Lung Diseases | Odonto-onycho-dermal Dysplasia | Usher Syndrome Type III | Nevus | Heart Septal Defects | Incontinentia Pigmenti | Oculocutaneous Albinism Type 1 | Spinal Muscular Atrophy Type 2 | Osteonecrosis Of The Jaw | Dementia, Vascular | Lichen Planus | Cervical Dystonia | Sjogren Syndrome | Endometritis | Narcolepsy | Purpura, Thrombotic Thrombocytopenic | Takenouchi-Kosaki Syndrome | Discoid Lupus Erythematosus | Malonyl-CoA Decarboxylase Deficiency | Hyperkeratosis | Migraine | Still Disease | Fibrodysplasia Ossificans Progressiva | Choriocarcinoma | Sturge-Weber Syndrome | Preaxial Polydactyly | Carcinoma In Situ | Spinocerebellar Ataxia Type 40 | Dermatitis | Papilloma | Polycythemia | REM Sleep Behavior Disorder | Neurotoxicity | 3-hydroxyacyl-CoA Dehydrogenase Deficiency | Mucolipidosis Type IV | Noonan Syndrome | Werner's Syndrome | Congenital Mirror Movements | Generalized Epilepsy And Paroxysmal Dyskinesia | Spinocerebellar Ataxia Type 14 | Charcot-Marie-Tooth Disease, Type 2C | Keratoacanthoma | Autoimmune Polyendocrine Syndrome | Chitayat Syndrome | Axenfeld-Rieger Syndrome | Alexander Disease | Hydrops Fetalis | Varices | Leishmaniasis, Cutaneous | Gout | Hypopigmentation | Epicondylitis | Sarcoidosis, Pulmonary | Menetrier Disease | Empyema | Premature Ejaculation | Schwartz-Jampel-Aberfeld Syndrome | Blepharitis | Aromatic L-amino Acid Decarboxylase Deficiency | Thyroid Hormone Resistance | Hepatitis D | Osteogenesis Imperfecta | Stuttering | Abetalipoproteinemia | Periventricular Leukomalacia | 3-M Syndrome | Learning Disability | Facioscapulohumeral Muscular Dystrophy Type 2 | Heroin Dependence | Cohen Syndrome | Adenomyosis | Diabetes Type 2 | Lattice Corneal Dystrophy Type 1 | Nestor-Guillermo Progeria Syndrome | Uremic Pruritus | Compartment Syndrome | Thalassemia | Hartnup Disease | Hyperinsulinemia | Colitis, Microscopic | Ischemia | Hepatitis E | Neuropathy | Lichen Sclerosus | Chorea | Pearson Syndrome | Argininosuccinic Aciduria | Myoclonus-dystonia Syndrome | Epidermolysis Bullosa Simplex, Generalized | Trismus-pseudocamptodactyly Syndrome | Focal Facial Dermal Dysplasia | HUPRA Syndrome | Ependymoma | Skin Fragility-woolly Hair Syndrome | Papillon-Lefevre Syndrome | Constipation | Pseudohypoaldosteronism | Hyperoxaluria | Phosphoenolpyruvate Carboxykinase Deficiency, Cytosolic | Paronychia | Chylomicron Retention Disease | Multiple Mitochondrial Dysfunctions Syndrome Type 1 | Mucolipidosis | Hypercholesterolemia, Familial | Hemolytic Anemia | Vascular Calcification | X-linked Sideroblastic Anemia | Polycystic Ovary Syndrome | Epidermolysis Bullosa Simplex, Localized | Molybdenum Cofactor Deficiency | Acute Leukemia | Peutz-Jeghers Syndrome | Sensory Neuropathy | Herpes Genitalis | Diabetes | Hemochromatosis Type 1 | Restless Legs Syndrome | Stroke, Hemorrhagic | Gyrate Atrophy Of The Choroid And Retina | Mast Cell Leukemia | Epidermolysis Bullosa | Hyperparathyroidism, Primary | Hemangioma | Gynecomastia | Obsessive-compulsive Disorder | Macular Corneal Dystrophy Type 1 | Cutaneous T-cell Lymphoma | Chondrodysplasia Punctata 1, X-linked Recessive | Hereditary Hemorrhagic Telangiectasia Type 2 | Ocular Hypertension | Bronchitis, Chronic | Congenital Ichthyosiform Erythroderma | Combined Pituitary Hormone Deficiency | Dystrophy, Cone-rod | Familial Hypertrophic Cardiomyopathy | Infantile Refsum Disease | Pseudohermaphroditism | Multiple Sclerosis | Sengers Syndrome | Bleeding Disorder Due To CalDAG-GEFI Deficiency | Thrombophilia | Fanconi Anemia | Hypotrichosis | Optic Neuritis | Synovitis | Sarcoma, Endometrial Stromal | Wieacker-Wolff Syndrome | Carpenter Syndrome | Hypertrophic Osteoarthropathy, Primary, Autosomal Recessive 1 | Hypoproteinemia, Hypercatabolic | Endometrial Hyperplasia | Toxoplasmosis | Coffin-Siris Syndrome | Galloway-Mowat Syndrome | Hypokalemic Periodic Paralysis | Otitis Media | Epidermolysis Bullosa Simplex, Dowling-Meara Type | Hereditary Mixed Polyposis Syndrome | Toxic Epidermal Necrolysis | Pituitary Stalk Interruption Syndrome | Vitelliform Macular Dystrophy | Keloid | Seborrheic Dermatitis | Eosinophilia | Neural Tube Defect | Hernia, Inguinal | Astigmatism | Osteogenesis Imperfecta Type IV | Portal Vein Thrombosis | Congenital Disorders Of Glycosylation | VACTERL/VATER Association | Corneal Neovascularization | Raynaud Phenomenon | Myasthenia Gravis | Diabetes Mellitus, Transient Neonatal | Glycogen Storage Disease | Microphthalmia, Syndromic 7 | Spondylosis | Angioedema, Hereditary | Scleroderma, Diffuse | Panuveitis | Retinal Degeneration | Dysgerminoma | Myelofibrosis | Liver Failure, Acute Infantile | Enterocolitis, Necrotizing | Hemolytic Uremic Syndrome, Atypical | Holoprosencephaly | Leukemia-lymphoma, Adult T-cell | Acrocallosal Syndrome | Fundus Albipunctatus | Bruck Syndrome | Pancreatitis, Chronic | Lymphoproliferative Disease, X-linked | Camurati-Engelmann Disease | Dyslipidemia | Familial Isolated Hyperparathyroidism | Anorectal Fistula | Eccrine Porocarcinoma | Combined Deficiency Of Factor V And Factor VIII | Choroideremia | Dysequilibrium Syndrome | Pemphigus Vulgaris | Neutrophilia | Oculocutaneous Albinism Type 2 | Polyarteritis Nodosa | Alpha-mannosidosis | Bethlem Myopathy | Primary Aldosteronism | Arthropathy | Lymphopenia | Bloom Syndrome | Trigonocephaly | Sleep Disorder | Cryopyrin-associated Periodic Syndromes | Carbamoyl Phosphate Synthetase I Deficiency | Adenoma, Pleomorphic | Usher Syndrome Type I | Glutathione Synthetase Deficiency | Fontaine Progeroid Syndrome | Chronic Idiopathic Myelofibrosis | ADNP Syndrome | Cholestasis | Encephalopathy, Hepatic | Cellulitis | Encephalopathy, Ethylmalonic | Persistent Fetal Circulation | Hypersomnia | Avian Influenza | Pernicious Anemia | Mycosis Fungoides | Progressive Familial Intrahepatic Cholestasis Type 1 | Chromosome 17q21.31 Deletion Syndrome | Gallstones | Creatine Deficiency Syndrome | Noonan Syndrome-like Disorder With Loose Anagen Hair | Joubert Syndrome | Epilepsy, Generalized | Glutaric Aciduria Type 1 | Pityriasis Rubra Pilaris | Panniculitis | Cornelia De Lange Syndrome | Lesch-Nyhan Syndrome | Filariasis | Platelet Disorders | Erythema Nodosum | Schnitzler Syndrome | Multifocal Motor Neuropathy | Glaucoma | Erysipelas | Mitochondrial Encephalomyopathy | Otopalatodigital Syndrome Type 2