Disease

Craniopharyngioma

About the Disease
Craniopharyngioma, also known as dysodontogenic epithelial tumor, is related to papillary craniopharyngioma and adamantinous craniopharyngioma, and has symptoms including visual disturbance An important gene associated with Craniopharyngioma is APC (APC Regulator Of WNT Signaling Pathway), and among its related pathways/superpathways are Signal Transduction and Nanog in Mammalian ESC Pluripotency. The drugs Prednisone and Hydrocortisone have been mentioned in the context of this disorder. Affiliated tissues include pituitary, hypothalamus and brain, and related phenotypes are abnormal hypothalamus morphology and cerebral calcification

Common Targets
RAF1 | APC | G673 | CTNNB1 | MAP2K2 | TMEM127 | METAP2 | RIPK3 | Dual Specificity Mitogen-Activated Protein Kinase Kinase (MEK) (nonspecified subtype) | MAP2K1

疾病靶点研报
Craniopharyngioma

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

Other Diseases

Diabetes Gestational | Progressive Myoclonic Epilepsy | Thrombasthenia | Depression | Hypertrophic Osteoarthropathy, Primary, Autosomal Recessive 2 | Spinocerebellar Ataxia Type 40 | Protein C Deficiency | Adrenoleukodystrophy, X-linked | Sickle Cell Anemia | Tylosis With Esophageal Cancer | Peters-plus Syndrome | Ameloblastoma | Oculocutaneous Albinism Type 2 | Astrocytoma | Encephalitis, Tick-borne | Hemangioma | Spondylosis | Blood Protein Disorders | Eclampsia | Nutrition Disorders | Retinal Telangiectasia | Renal Failure | Paracoccidioidomycosis | Histiocytosis | Primary Sclerosing Cholangitis | Familial Retinal Arterial Macroaneurysm | C3 Glomerulopathy | Krabbe Disease | Congenital Nystagmus | Glaucomatocyclitic Crisis | Congenital Stromal Corneal Dystrophy | Axenfeld-Rieger Syndrome | Hereditary Elliptocytosis | Ocular Hypertension | Measles | Nemaline Myopathy 10 | Metabolic Diseases | Ataxia-hypogonadism-choroidal Dystrophy Syndrome | Intestinal Hypomagnesemia 1 | Chondrodysplasia Punctata | Hepatitis D | Primary Pigmented Nodular Adrenocortical Disease | Poirier-Bienvenu Neurodevelopmental Syndrome | Sclerosteosis 2 | Myofibrillar Myopathy | Atrioventricular Septal Defect | Hyper IgE Syndrome | Harlequin Ichthyosis | Branchiootorenal Syndrome | Auriculocondylar Syndrome | Camurati-Engelmann Disease | Lymphoproliferative Disease, X-linked | Thrombophilia | Hypohidrotic Ectodermal Dysplasia | Galloway-Mowat Syndrome | Meesmann Corneal Dystrophy | Urticaria | Chiari Malformation Type I | Transthyretin-related Amyloidosis | Epidermolysis Bullosa Simplex, Localized | Lewy Body Dementia | Alpha-1 Antitrypsin Deficiency | Clouston Hidrotic Ectodermal Dysplasia | Spinocerebellar Ataxia Type 5 | Astigmatism | Congenital Absence Of Vas Deferens | Hypertensive Retinopathy | Urethritis | Diffuse Idiopathic Pulmonary Neuroendocrine Cell Hyperplasia | Schistosomiasis Mansoni | Dermatomyositis | Donnai-Barrow Syndrome | Epithelioid Hemangioma | Gliosarcoma | Pneumonia, Viral | Spinal Cord Diseases | Retinal Coloboma | Mast Cell Leukemia | Goiter | Camptocormia | Ameloblastic Carcinoma | Epilepsy | Rubinstein-Taybi Syndrome | Spinocerebellar Ataxia Type 2 | Zygomycosis | Chorea-acanthocytosis | Aceruloplasminemia | Chitayat Syndrome | Hemophilia | Marshall-Smith Syndrome | Hemolytic Uremic Syndrome | Polymyositis | Jacobsen Syndrome | Lymphangiomatosis | Esophageal Adenocarcinoma | Hypokalemia | Uveitis | Paroxysmal Nocturnal Hemoglobinuria | Geleophysic Dysplasia | Pulmonary Veno-occlusive Disease | Hyperferritinemia-cataract Syndrome | Triphalangeal Thumb-polysyndactyly Syndrome | Diabetic Neuropathy | Cerebellofaciodental Syndrome | AIDS | Proctitis | Progressive Familial Intrahepatic Cholestasis Type 1 | Angiomyolipoma | Meningioma, Benign | Spondylocostal Dysostosis | Syndactyly | Vasculitis | Ichthyosis | Asphyxia Neonatorum | Epiphyseal Chondrodysplasia, Miura Type | Microcephalic Osteodysplastic Primordial Dwarfism, Type II | Primary Hyperoxaluria Type 3 | Acromicric Dysplasia | Hepatitis, Autoimmune | Meniere's Disease | Meconium Ileus | Glaucoma, Congenital | Exocrine Pancreatic Insufficiency | Spinocerebellar Ataxia Type 31 | Beta-Propeller Protein-associated Neurodegeneration | Gray Platelet Syndrome | Sialidosis | Pyruvate Carboxylase Deficiency Disease | Micro Syndrome | Cancer, Kidney | Nanophthalmos | Prurigo Nodularis | Benign Familial Neonatal Convulsions | Genee-Wiedemann Syndrome | Spitzoid Melanoma | Sickle Cell Disease | Acute Leukemia | Non-small Cell Lung Cancer | Basal Ganglia Disease | Huntington's Disease | Weill-Marchesani Syndrome | Juvenile Myoclonic Epilepsy | Charcot-Marie-Tooth Disease Type 4B1 | Unverricht-Lundborg Syndrome | Microcephaly, Seizures, And Developmental Delay | Cleidocranial Dysplasia | Achondrogenesis | Apert Syndrome | Temtamy Preaxial Brachydactyly Syndrome | Dysferlinopathy | Castleman Disease | Enterocolitis, Necrotizing | Necrobiosis Lipoidica | Waardenburg Syndrome Type 2 | Anxiety Disorders | Encephalopathy, Hepatic | Corneal Neovascularization | Hyperandrogenemia | Craniofacial Dysostosis | Burn-McKeown Syndrome | X-linked Sideroblastic Anemia | KBG Syndrome | Dengue Shock Syndrome | Anuria | Cherubism | Epidermolysis Bullosa Acquisita | Progressive Osseous Heteroplasia | Arterial Tortuosity Syndrome | Sarcoidosis, Pulmonary | Anorectal Malformations | Bipolar Disorder | Hemangioblastoma | Oculocutaneous Albinism Type 4 | Charcot-Marie-Tooth Disease Type 2E | Peyronie's Disease | Osteonecrosis | Paraganglioma, Carotid Body | Keratocystic Odontogenic Tumor | Non-Hodgkin Lymphoma | Metachromatic Leukodystrophy | Pulmonary Sclerosing Hemangioma | Epidermolysis Bullosa Simplex | Chorea | Congenital Ichthyosiform Erythroderma | Myoclonic Atonic Epilepsy | Basal Ganglia Cerebrovascular Disease | Pterygium | HIBCH Deficiency | Cerebral Cavernous Malformations | Malignant Fibrous Histiocytoma | Guillain-Barre Syndrome | Alpha-mannosidosis | Gaze Palsy, Familial Horizontal, With Progressive Scoliosis, 2 | Malaria, Cerebral | 6-pyruvoyl-tetrahydropterin Synthase Deficiency | Sensorineural Hearing Loss | Biotinidase Deficiency | Aldosterone Synthase Deficiency | Pseudohypoparathyroidism Type 1A | Infantile Nephropathic Cystinosis | Schizophrenia, Paranoid | Treacher Collins Syndrome | Neovascular Glaucoma | Alzheimer Disease, Late Onset | Vitreoretinal Degeneration, Snowflake Type | Primary Hyperoxaluria Type 1 | Recurrent Respiratory Papillomatosis | Myopia | Bruck Syndrome | B-cell Chronic Lymphocytic Leukemia | Tyrosinemia Type 1 | Hyperparathyroidism | Dyslexia | Leiomyoma | Gastroenteritis, Eosinophilic | Hyperphenylalaninemia | Bartter Syndrome | Fahr Disease | Glycogen Storage Disease Type 9 | Pneumonia, Mycoplasma | Muscular Dystrophy | Multiple System Atrophy | Follicular Dendritic Cell Sarcoma | Alazami Syndrome | Osteoporosis | Jaundice, Obstructive | Inborn Errors Of Metabolism | Open-angle Glaucoma | Tinea | Pyloric Stenosis, Infantile Hypertrophic | Endocarditis | Schindler Disease | Angioedema, Hereditary | Cartilage Disorders | Hemangioendothelioma | Antithrombin III Deficiency | Learning Disability | Erythromelalgia | Postpoliomyelitis Syndrome | Androgenic Alopecia | Spinocerebellar Ataxia Type 16 | Metanephric Adenoma | Autonomic Neuropathy | Cryptosporidiosis | Lichen Planus | Pemphigus | Blepharophimosis Syndrome | Frank-ter Haar Syndrome | Nevus | Dystonia Musculorum Deformans | Hemoglobinopathies | Leprosy | Stromal Corneal Dystrophy | Wolff-Parkinson-White Syndrome | Rheumatoid Arthritis | Retinitis Pigmentosa 3 | Schwannoma | Chronic Inflammatory Demyelinating Polyneuropathy | Leiomyosarcoma | Multiple Congenital Anomalies-hypotonia-seizures Syndrome 2 | Aneurysm, Abdominal Aortic | Metaphyseal Chondrodysplasia, Schmid Type | Hyperostosis | Dermatitis Herpetiformis | Congenital Hypofibrinogenemia | Macular Corneal Dystrophy | Fibrosarcoma | Pigment Dispersion Syndrome | Autosomal Recessive Bestrophinopathy | Vitelliform Macular Dystrophy | Sarcoma | Vitamin K Deficiency | Crimean-Congo Hemorrhagic Fever | Hypotrichosis, Congenital, With Juvenile Macular Dystrophy | Nicotine Addiction | Tietze Syndrome | Waardenburg Syndrome Type 4 | Hypercalciuria | Atopic Dermatitis | Huntington's Disease-like 2 | Liver Diseases | Hypomyelination With Atrophy Of Basal Ganglia And Cerebellum | Lipid Storage Diseases | Gilbert Syndrome | Wolman Disease | Dysfibrinogenemia | Osteogenesis Imperfecta Type IV | Ichthyosis Hystrix, Curth-Macklin Type | Hypoalbuminemia | Bardet-Biedl Syndrome | Joubert Syndrome 2 | Ghosal Syndrome | Fetal Alcohol Syndrome | Isobutyryl-CoA Dehydrogenase Deficiency | Rheumatic Heart Disease | Li-Fraumeni Syndrome | Lipid Storage Myopathy | Infertility | Agammaglobulinemia | Sleep Apnea, Central | Frontotemporal Dementia With Amyotrophic Lateral Sclerosis | Progressive Encephalopathy-optic Atrophy Syndrome | Spermatocele | Farber Disease | Light Chain Amyloidosis | Brenner Tumor | Non-epidermolytic Palmoplantar Keratoderma | Salla Disease | Acral Lentiginous Melanoma | Pseudomyxoma Peritonei | Allergic Contact Dermatitis | Kashin-Beck Disease | Autoimmune Hemolytic Anemia | Lattice Corneal Dystrophy | Glycogen Storage Disease Type 1b | Multicystic Renal Dysplasia | Gigantism | Klinefelter Syndrome | Leber Hereditary Optic Neuropathy | Richter's Syndrome | Polycythemia Vera | Thyroid Dyshormonogenesis | ICF Syndrome | Short-chain Acyl-CoA Dehydrogenase Deficiency | Congenital Aniridia | Amenorrhea | Ophthalmia, Sympathetic | Congenital Generalized Lipodystrophy | Maple Syrup Urine Disease | Hypolipoproteinemia | Mucolipidosis | Williams Syndrome | Osteogenesis Imperfecta | Spinocerebellar Ataxia Type 1 | Schistosomiasis | Cutis Laxa | Polycythemia | Stroke, Ischemic | Dent Disease | Central Pain Syndrome | Acute Motor Axonal Neuropathy | Congenital Disorders Of Glycosylation Type II | Tetraplegia | Mosaic Variegated Aneuploidy Syndrome 2 | Parkinson's Disease | Cranioectodermal Dysplasia | Juvenile Hyaline Fibromatosis | Poretti-Boltshauser Syndrome | Hereditary Coproporphyria | Idiopathic Multicentric Castleman Disease | Eczema | Lymphoma, B-cell | Megaloblastic Anemia | Hemorrhagic Disorders | Common Cold | Androgen Insensitivity | Diffuse Palmoplantar Keratoderma | Amblyopia | Periventricular Leukomalacia | Nephritis, Interstitial | Disseminated Intravascular Coagulation | Varices | Nephrocalcinosis | Alopecia Areata | Osmotic Demyelination Syndrome | Colon Adenoma | Cushing Syndrome | Porencephaly | Rothmund-Thomson Syndrome | Generalized Epilepsy And Paroxysmal Dyskinesia | Johanson-Blizzard Syndrome | Craniofrontonasal Syndrome | Cholesteryl Ester Storage Disease | Blue Rubber Bleb Nevus Syndrome | Autoimmune Polyendocrine Syndrome | Vertebrobasilar Insufficiency | Pregnancy, Ectopic | NDH Syndrome | Chromosome 16p11.2 Deletion Syndrome | Takenouchi-Kosaki Syndrome | Chronic Mucocutaneous Candidiasis | Twin-to-twin Transfusion Syndrome | Chromosome 9q34.3 Deletion Syndrome | Eating Disorder | Benign Hereditary Chorea | Hypermethioninemia | Spinocerebellar Ataxia Type 13 | Larsen Syndrome | Spinal Muscular Atrophy Type 2 | Thymoma, Malignant | Restless Legs Syndrome | Lipid Metabolism Disorders | Encephalopathy, Ethylmalonic | Overactive Bladder | Toxic Epidermal Necrolysis | Hypophosphatemic Rickets, Autosomal Recessive, 1 | Hypothalamic Obesity | Hidradenitis Suppurativa | Autoimmune Disease | Hyperhomocysteinemia