Disease

Combined Pituitary Hormone Deficiency

About the Disease
Pituitary Hormone Deficiency, Combined, 2, also known as panhypopituitarism, is related to pituitary hormone deficiency, combined or isolated, 1 and panhypopituitarism, x-linked. An important gene associated with Pituitary Hormone Deficiency, Combined, 2 is PROP1 (PROP Paired-Like Homeobox 1), and among its related pathways/superpathways are Signal Transduction and Class A/1 (Rhodopsin-like receptors). The drugs Epitestosterone and Oxytocin have been mentioned in the context of this disorder. Affiliated tissues include pituitary, thyroid and brain, and related phenotypes are hypothyroidism and short stature

Common Targets
G4089 | PROKR2 | OTX2 | HESX1 | GLI2 | BMP4 | OTP | LHX2 | LHX4 | HHIP | NR4A1 | GNRH1 | EYA4 | CHD7 | FGF8 | FGFR1 | HMX2 | E2F4 | LHX3 | POU1F1 | RNPC3 | ALMS1 | CDON | PROP1 | SHH | ZIC2 | SEMA3A | HES1 | WDR11 | SRA1 | TSHZ1 | PCSK1

疾病靶点研报
Combined Pituitary Hormone Deficiency

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

Other Diseases

CHARGE Syndrome | Dysgerminoma | Neutropenia | Spondyloarthritis | Neuronal Ceroid Lipofuscinosis | Epidermolysis Bullosa Simplex With Mottled Pigmentation | Filariasis | Angioimmunoblastic T-cell Lymphoma | Paroxysmal Nocturnal Hemoglobinuria | Charcot-Marie-Tooth Disease Type 4E | Anti-NMDA Receptor Encephalitis | Neurodevelopmental Disorder With Central Hypotonia And Dysmorphic Facies | Bronchitis | Harlequin Ichthyosis | Hyperinsulinemic Hypoglycemia | Patent Foramen Ovale | Parapsoriasis | Galactosialidosis | Rhabdoid Tumor | Mast Cell Leukemia | HUPRA Syndrome | Hemorrhage | Kawasaki Disease | Hyperbilirubinemia | Riboflavin Transporter Deficiency Neuronopathy | Uveitis, Anterior | Pyelonephritis | Kashin-Beck Disease | Hennekam Lymphangiectasia-lymphedema Syndrome | Borjeson-Forssman-Lehmann Syndrome | Spinocerebellar Ataxia Type 38 | Zollinger-Ellison Syndrome | CDKL5 Deficiency Disorder | Encephalitis | Trismus-pseudocamptodactyly Syndrome | Neurodegeneration With Brain Iron Accumulation | Coenzyme Q10 Deficiency | Leukoplakia | Combined Deficiency Of Factor V And Factor VIII | Lipoma | Agammaglobulinemia | Gastritis, Atrophic | Sarcoma, Ewing | Familial Dysautonomia | Double Outlet Right Ventricle | Cousin Syndrome | Goiter | Neurodermatitis | Early Infantile Epileptic Encephalopathy 13 | Erythema Multiforme | Citrullinemia | Stargardt Disease | 3-methylglutaconic Aciduria Type IV | Peters-plus Syndrome | Hepatitis, Chronic | Pyruvate Dehydrogenase Deficiency | Bronchiolitis | Triphalangeal Thumb-polysyndactyly Syndrome | Hypoglycemia | Tyrosinemia Type 2 | Niemann-Pick Disease, Type A | Primary Biliary Cholangitis | Hypertelorism | Usher Syndrome Type I | Branchiootorenal Syndrome | Scleritis | Wagner Disease | Macular Corneal Dystrophy | Congenital Sodium Diarrhea | Cholangitis | Cole-Carpenter Syndrome | Diabetic Nephropathy | Coffin-Siris Syndrome | Oculocutaneous Albinism Type 1 | NDH Syndrome | Lymphoma Lymphoblastic | GNE Myopathy | Benign Hereditary Chorea | Hemochromatosis Type 1 | Multiple Congenital Anomalies-hypotonia-seizures Syndrome 2 | Vitamin A Deficiency | Myelofibrosis | Calcium Pyrophosphate Deposition Disease | B-cell Chronic Lymphocytic Leukemia | Multiple Sclerosis, Primary Progressive | Congenital Primary Aphakia | Kearns-Sayre Syndrome | Rash | Fontaine Progeroid Syndrome | Gnathodiaphyseal Dysplasia | Craniofacial Dysostosis | Spinocerebellar Ataxia Type 27 | Aplasia Cutis Congenita | Nemaline Myopathy | Thalassemia | Cherubism | Rothmund-Thomson Syndrome | Pure Red Cell Aplasia | Galactosemia | Hyperinsulinism-hyperammonemia Syndrome | Diastrophic Dysplasia | Distal Myopathy | Cellulitis | Alpers Syndrome | Palsy, Cerebral | Gastroenteritis | Premature Ejaculation | Thrombophlebitis | Congenital Dyserythropoietic Anemia Type 1 | Glycogen Storage Disease Type 0 | Non-small Cell Lung Cancer | Pterygium | Metanephric Adenoma | Maternally Inherited Diabetes And Deafness | Metatropic Dysplasia | Sick Sinus Syndrome 1 | Cardiomyopathy, Restrictive | Atrial Septal Defect | Ligneous Conjunctivitis | Muir-Torre Syndrome | Paraganglioma | REM Sleep Behavior Disorder | Robinow Syndrome | Epidermolytic Palmoplantar Keratoderma | Hypermethioninemia | Myelitis, Transverse | Cone Dystrophy | Tic Disorder | Sertoli Cell-only Syndrome | Carbamoyl Phosphate Synthetase I Deficiency | Lipid Storage Diseases | Angiodysplasia | Personality Disorders | Aphasia | Retinopathy, Diabetic | Silicosis | Schizophrenia, Paranoid | Muscle Wasting | Intellectual Disability, Autosomal Dominant 5 | Acute Lung Injury | Acute Motor Axonal Neuropathy | Ameloblastoma | Occipital Neuralgia | KBG Syndrome | Exocrine Pancreatic Insufficiency | Klippel-Feil Syndrome | Joubert Syndrome 2 | Epiphyseal Chondrodysplasia, Miura Type | Potocki-Shaffer Syndrome | Fatty Aldehyde Dehydrogenase Deficiency | Mitochondrial Encephalomyopathy | Progressive Myoclonic Epilepsy | Panic Disorder | Miyoshi Myopathy | Johanson-Blizzard Syndrome | Bronchiectasis | Heavy Chain Disease | Sulfite Oxidase Deficiency | Ophthalmia, Sympathetic | Microcephalic Osteodysplastic Primordial Dwarfism, Type I | Cranioectodermal Dysplasia | Sweet Syndrome | Migraine | Donnai-Barrow Syndrome | Pancreatitis, Chronic | Spasticity | Supravalvular Aortic Stenosis | Sarcomatoid Carcinoma Of The Lung | Major Depression | Sickle Cell Disease | Myopathy | Campomelic Dysplasia | Waardenburg Syndrome | Erdheim-Chester Disease | Interstitial Lung Diseases | Tonsillitis | COACH Syndrome | Myelitis | LRBA Deficiency | Raine Syndrome | Arthritis | Medulloblastoma | Brooke-Spiegler Syndrome | Peeling Skin Syndrome Type B | Agnathia-Otocephaly Complex | Pyruvate Kinase Deficiency | Non-bullous Congenital Ichthyosiform Erythroderma | Primrose Syndrome | Angiomyolipoma | Graves Disease | Congenital Nystagmus | Proctitis | Congenital Aniridia | Diabetes Insipidus, Nephrogenic | Holoprosencephaly | Tuberculosis | Intracranial Hypertension | Toxic Epidermal Necrolysis | Osteogenesis Imperfecta Type III | Liebenberg Syndrome | Traboulsi Syndrome | Spinocerebellar Ataxia Type 40 | Vertigo | CEDNIK Syndrome | Congenital Myopathy | Neurofibromatosis | Uveitis | Infertility, Male | Cardiofaciocutaneous Syndrome | Whipple's Disease | Depression | High Molecular Weight Kininogen Deficiency | Pierpont Syndrome | Tietze Syndrome | Meconium Ileus | Hypoproteinemia, Hypercatabolic | Blepharoconjunctivitis | Pituitary Disorders | Disseminated Intravascular Coagulation | Primary Sclerosing Cholangitis | Asplenia | Brenner Tumor | Cystinosis | Cyst | Eosinophilia | Autosomal Recessive Congenital Ichthyosis | Perry Syndrome | Photosensitivity | Spondyloperipheral Dysplasia | Hypophosphatasia | Thyroid Dysgenesis | Bacterial Meningitis | Myositis, Focal | DiGeorge Syndrome | Choriocarcinoma | Metabolic Diseases | Neurofibromatosis Type 1 | Conjunctivitis, Allergic | Amelanotic Melanoma | Dent Disease | Cutaneous Lupus Erythematosus | Rheumatic Heart Disease | Autosomal Recessive Spastic Paraplegia Type 35 | Congenital Torticollis | Cyclic Vomiting Syndrome | Arthritis, Gouty | Lymphoproliferative Disorders | Cancer, Breast | Thrombocytopenia | Impetigo | Facioscapulohumeral Muscular Dystrophy Type 2 | Tuberculous Meningitis | Idiopathic Multicentric Castleman Disease | Acrocallosal Syndrome | Hypocalcemia | Gout | Erythromelalgia | Frontometaphyseal Dysplasia | Ulcerative Colitis | Presbycusis | Vitiligo | Neuroblastoma | Microcephalic Osteodysplastic Primordial Dwarfism, Type II | Takayasu's Arteritis | Synovitis | Wolcott-Rallison Syndrome | Intestinal Pseudo-obstruction | Lactose Intolerance | Chorea | Overactive Bladder | Mucolipidosis Type II | Ovarian Sex Cord-stromal Tumor | IMAGe Syndrome | Kernicterus | Neuroendocrine Cancer | Bullous Pemphigoid | Neurocutaneous Syndromes | Hypertension, Renovascular | Myasthenia | Glycogen Storage Disease Type 1b | Mitochondrial Myopathy | Congenital Fiber-type Disproportion Myopathy | Waardenburg Syndrome Type 2E | Sclerocornea | Pseudoachondroplasia | Dyskeratosis Congenita | Sitosterolemia | Gardner Syndrome | Polycythemia | Meningococcal Infections | Corneal Edema | Juvenile Polyposis | Congenital Hereditary Endothelial Dystrophy Type I | Lipid Metabolism Disorders | Recurrent Respiratory Papillomatosis | Microphthalmia | Papillon-Lefevre Syndrome | Idiopathic Pulmonary Fibrosis | Diabetic Encephalopathy | Neutrophilia | Schnitzler Syndrome | Reflex Epilepsy | Shock, Cardiogenic | Angioedema, Acquired | Orthostatic Intolerance | Lissencephaly 2 | Temtamy Preaxial Brachydactyly Syndrome | Mixed Connective Tissue Disease | Neuromyotonia | 6-pyruvoyl-tetrahydropterin Synthase Deficiency | Thymoma, Malignant | Large Granular Lymphocytic Leukemia | Leukoplakia, Oral | Autism | Restrictive Dermopathy | Wolff-Parkinson-White Syndrome | Arterial Tortuosity Syndrome | Spinocerebellar Ataxia Type 23 | Mycosis Fungoides | Myhre Syndrome | X-linked Acrogigantism | Multiple Sclerosis, Secondary Progressive | Fukuyama Congenital Muscular Dystrophy | Fascioliasis | Primary Ovarian Insufficiency | Trichomegaly | Spinocerebellar Ataxia Type 14 | Hepatopulmonary Syndrome | Ectopia Lentis, Isolated, Autosomal Recessive | Combined Malonic And Methylmalonic Acidemia | Hypogammaglobulinemia | D-2-Hydroxyglutaric Aciduria | Gaze Palsy, Familial Horizontal, With Progressive Scoliosis, 2 | Bronchitis, Chronic | Cheilitis | Lung Diseases | Epidermolysis Bullosa Simplex, Localized | Carpal Tunnel Syndrome | Genitopatellar Syndrome | Papilloma | Cardiac Arrest | Keratoconus | Dominant Optic Atrophy | Pitt-Hopkins Syndrome | Evans Syndrome | Sarcoma, Endometrial Stromal | Erectile Dysfunction | Cerebral Cavernous Malformations | Keratocystic Odontogenic Tumor | Pneumoconiosis | Charcot-Marie-Tooth Disease Type 3 | Chordoid Glioma | Encephalopathy | Angina Pectoris | Postpartum Depression | Mandibuloacral Dysplasia With Type A Lipodystrophy | Cocaine-Related Disorders | Localized Scleroderma | Varicocele | Esophagitis | Richter's Syndrome | Rosacea | Keratosis | Autoimmune Polyendocrine Syndrome | Hepatic Adenomatosis | Erythropoietic Protoporphyria | Cataract | Dysplastic Nevus | Hyperphenylalaninemia | Thyroiditis | HANAC Syndrome | Stiff-man Syndrome | Esophageal Carcinoma | Intestinal Tuberculosis | Hyperekplexia | Melnick-Needles Syndrome | Cystinuria | Vascular Calcification | Hemophagocytic Lymphohistiocytosis | Agoraphobia | Congenital Diaphragmatic Hernia | Trachoma | Polymyositis | Thyrotoxic Periodic Paralysis | Adult Polyglucosan Body Disease | Spondylocostal Dysostosis | Nail-Patella Syndrome | Infantile Neuroaxonal Dystrophy | Tangier Disease | Measles | GAPO Syndrome | Apraxia | Learning Disability | Glycogen Storage Disease Type 6 | Hypophosphatemic Rickets, Autosomal Recessive, 1 | Porokeratosis | Periventricular Nodular Heterotopia | Distal Spinal Muscular Atrophy | Lymphoma | Lymphoma, Primary Cutaneous Anaplastic Large Cell