Chordoid Glioma

About the Disease
Chordoid Glioma, also known as chordoid glioma of the third ventricle, is related to third ventricle chordoid glioma and obstructive hydrocephalus. An important gene associated with Chordoid Glioma is PRKCA (Protein Kinase C Alpha). The drugs Dabrafenib and Trametinib have been mentioned in the context of this disorder. Affiliated tissues include brain, hypothalamus and eye.

Common Targets
PRKCA | G673

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

Other Diseases

Micropenis | Adenosine Deaminase 2 Deficiency | Urofacial Syndrome | Noonan Syndrome-like Disorder With Loose Anagen Hair | Kaposi Sarcoma | Focal Facial Dermal Dysplasia | Cyclic Vomiting Syndrome | Botulism | Glioma | Cherubism | Encephalitis, Tick-borne | Autoimmune Polyendocrine Syndrome | Duane Retraction Syndrome | Tenosynovial Giant Cell Tumor | Chorioretinitis | Tay-Sachs Disease | Rosacea | Maple Syrup Urine Disease | Polyomavirus Nephropathy | Waardenburg Syndrome Type 2 | Congestive Heart Failure | Fahr Disease | Alazami Syndrome | Harlequin Ichthyosis | Metabolic Diseases | Protein C Deficiency | Language Disorders | Seminoma | Vestibular Disease | Babesiosis | Hypokalemia | Amyotrophic Lateral Sclerosis | Diabetic Encephalopathy | Familial Retinal Arterial Macroaneurysm | Martsolf Syndrome | Urolithiasis | Early Infantile Epileptic Encephalopathy 28 | Lymphomatoid Granulomatosis | Heterotopic Ossification | Lymphoproliferative Disease, X-linked | Macrophagic Myofasciitis | Metachromatic Leukodystrophy | Chronic Myelomonocytic Leukemia | Zygomycosis | Hemoglobinopathies | Strabismus | Phenylketonuria | Fontaine Progeroid Syndrome | Sclerosteosis | Cluster Headache | Stickler Syndrome | Acrodermatitis | Cerebellofaciodental Syndrome | Fundus Albipunctatus | Down Syndrome | Congenital Ichthyosiform Erythroderma | Tic Disorder | Hydrocephalus | Eclampsia | Biotinidase Deficiency | Hodgkin Lymphoma | Mitochondrial DNA Depletion Syndrome, Encephalomyopathic Form | Combined Pituitary Hormone Deficiency | Sitosterolemia | Antiphospholipid Syndrome | Niemann-Pick Disease, Type C | Hemimegalencephaly | Congenital Generalized Lipodystrophy | Canavan Disease | Chiari Malformation Type I | Hennekam Lymphangiectasia-lymphedema Syndrome | Osmotic Demyelination Syndrome | Myofibrillar Myopathy | CHOPS Syndrome | Hepatitis C, Chronic | Antley-Bixler Syndrome | Hypertension, Renovascular | Epilepsy Of Infancy With Migrating Focal Seizures | Congenital Bilateral Absence Of Vas Deferens | Craniosynostosis | Dermatitis | Headache | Retinopathy, Diabetic | Vitelliform Macular Dystrophy | Postpartum Depression | Mucormycosis | Lymphoma, AIDS-related | Rash | Methylmalonic Acidemia | Epithelioid Hemangioma | X-linked Creatine Transporter Deficiency | Gastritis, Atrophic | Huntington's Disease | Sleep Apnea, Obstructive | Dubin-Johnson Syndrome | Fanconi Anemia | Guanidinoacetate Methyltransferase Deficiency | Gastrointestinal Disorders | Long QT Syndrome Type 2 | Charcot-Marie-Tooth Disease Type 3 | Angina Pectoris | Porphyria | Antenatal Bartter Syndrome Type 1 | Spinal Muscular Atrophy | Acromegaly | Hidradenitis Suppurativa | Panniculitis | Smoldering Myeloma | Keratitis-ichthyosis-deafness Syndrome | Inflammatory Bowel Disease | Supravalvular Aortic Stenosis | Neuromyotonia | Cocaine-Related Disorders | Diabetes Gestational | Usher Syndrome Type II | Aldosterone Deficiency | Coronary Artery Disease | Lymphoma | Chromosome 17q21.31 Deletion Syndrome | Restrictive Dermopathy | 3-hydroxyacyl-CoA Dehydrogenase Deficiency | Ellis-Van Creveld Syndrome | Takotsubo Cardiomyopathy | Best Macular Dystrophy | Gerodermia Osteodysplastica | Lentigo | Cavitary Optic Disc Anomalies | Craniofacial Dysostosis | Brachydactyly | Prolymphocytic Leukemia | Glutaric Aciduria Type 2 | Chronic Beryllium Disease | Endometritis | Infertility, Male | Beta-Propeller Protein-associated Neurodegeneration | Hypotonia-cystinuria Syndrome | Multisystemic Smooth Muscle Dysfunction Syndrome | Microcephalic Primordial Dwarfism | Hyperekplexia | Wolfram Syndrome 2 | Kearns-Sayre Syndrome | Arthritis, Reactive | Poirier-Bienvenu Neurodevelopmental Syndrome | Trichuriasis | Gastroenteritis | Xeroderma Pigmentosum | Optic Nerve Diseases | Epithelial-myoepithelial Carcinoma | Primary Progressive Aphasia | Pupil Disorders | Incontinentia Pigmenti | Neurocutaneous Syndromes | HIBCH Deficiency | Sulfite Oxidase Deficiency | Melanocytic Nevus | Lung Diseases | Joubert Syndrome | Pulverulent Zonular Cataract | Robinow Syndrome | Lennox-Gastaut Syndrome | Charcot-Marie-Tooth Disease Axonal Type 2N | Cancer, Lung | Hydronephrosis | Evans Syndrome | Malonyl-CoA Decarboxylase Deficiency | Purpura | Skin Fragility-woolly Hair Syndrome | Brooke-Spiegler Syndrome | Myelomeningocele | Renal Hypomagnesemia 3 | Waardenburg Syndrome Type 2A | Pontocerebellar Hypoplasia Type 2 | Erysipelas | Vici Syndrome | Chronic Inflammatory Demyelinating Polyneuropathy | Retinal Dystrophy | Pelvic Inflammatory Disease | Pseudohypoaldosteronism | Roberts Syndrome | Glycogen Storage Disease Type 3 | Facioscapulohumeral Muscular Dystrophy Type 2 | Pheochromocytoma | Arterial Tortuosity Syndrome | Localized Scleroderma | Spondylometaphyseal Dysplasia | Hepatoblastoma | Craniometaphyseal Dysplasia | Primary Carnitine Deficiency | Hemochromatosis Type 1 | Alagille Syndrome | Lymphoproliferative Disorders | Subcortical Band Heterotopia | Myocardial Infarction | Muckle-Wells Syndrome | Asplenia | Nephritis, Interstitial | Uterine Leiomyoma | Pseudohypoparathyroidism Type 1C | 3-methylglutaconic Aciduria Type I | Lymphedema | Anal Fissure | Hypertensive Retinopathy | Waardenburg Syndrome Type 1 | Focal Dermal Hypoplasia | Saul-Wilson Syndrome | Gingivitis | Polycystic Kidney, Autosomal Recessive | Acromicric Dysplasia | Spermatocele | Glutaric Aciduria Type 1 | Ileitis | Hypertriglyceridemia | Peritonitis | CREST Syndrome | Behavioral Variant Of Frontotemporal Dementia | Tatton-Brown-Rahman Syndrome | Blood Protein Disorders | Lactose Intolerance | Thanatophoric Dysplasia Type 1 | Orthostatic Intolerance | Congenital Poikiloderma | Hyperlipidemia, Familial Combined | Combined Deficiency Of Factor V And Factor VIII | Chronic Leukemia | Bladder Exstrophy | Eiken Syndrome | VACTERL/VATER Association | Rickets | CEDNIK Syndrome | Congenital Myopathy | Lassa Fever | Tuberculosis | Fibrodysplasia Ossificans Progressiva | Pineoblastoma | Congenital Disorders Of Glycosylation | Perivascular Epithelioid Cell Tumor | Portal Vein Thrombosis | Uremia | Melanoma | Neural Tube Defect | Retinal Telangiectasia | Autosomal Recessive Spastic Paraplegia Type 75 | Pearson Syndrome | Hypotrichosis Simplex | Achromatopsia | Paraplegia | 3-methylglutaconic Aciduria Type IV | Trichomegaly | Osteosclerosis | Leukocyte Adhesion Deficiency | Sick Sinus Syndrome | Carcinoma, Squamous Cell | Nephroblastoma | Hypothalamic Obesity | 3-methylglutaconic Aciduria | Lipid Storage Myopathy | Ophthalmoplegia | Acromesomelic Dysplasia | Renal-hepatic-pancreatic Dysplasia | Pituitary Dwarfism | Short-chain Acyl-CoA Dehydrogenase Deficiency | Facioscapulohumeral Muscular Dystrophy Type 1 | Varices | Thrombosis | Alopecia Totalis | Subacute Sclerosing Panencephalitis | Androgenic Alopecia | Pulmonary Sclerosing Hemangioma | Autoimmune Autonomic Ganglionopathy | Takenouchi-Kosaki Syndrome | Tracheal Disorders | Diffuse Mesangial Sclerosis | Primary Hyperoxaluria Type 1 | Learning Disability | Pycnodysostosis | Hypotrichosis | Frontotemporal Dementia | Paraganglioma | Hepatitis, Chronic | Metachondromatosis | Depression | Cryptococcal Meningitis | Benign Familial Neonatal Convulsions | Scapuloperoneal Spinal Muscular Atrophy | NGLY1 Deficiency | Graft-versus-host Disease | Dengue Hemorrhagic Fever | Chondrodysplasia Punctata | Spondyloepimetaphyseal Dysplasia With Joint Laxity, Type 3 | Hyperammonemia | Conjunctivitis | Loeys-Dietz Syndrome Type 4 | Sengers Syndrome | PHARC Syndrome | Kabuki Syndrome | Spondyloepiphyseal Dysplasia Tarda, X-linked | Pyruvate Dehydrogenase Deficiency | Polycystic Ovary Syndrome | Specific Granule Deficiency | Myopia | Tyrosinemia Type 1 | Hereditary Spastic Paraplegia | Huntington's Disease-like 2 | Mitochondrial DNA Depletion Syndrome 13 | Malaria | Sensorineural Hearing Loss | Ameloblastic Carcinoma | Pleomorphic Xanthoastrocytoma | Rhizomelic Chondrodysplasia Punctata | Periventricular Leukomalacia | Delirium | Hypertelorism | Meckel-Gruber Syndrome | Mesothelioma, Malignant | Primary Hyperoxaluria | ICF Syndrome | Erectile Dysfunction | Prostatitis | Oculocutaneous Albinism Type 4 | Hemangioendothelioma | Krabbe Disease | Bronchitis | Traboulsi Syndrome | Corneal Ulcer | Osteoglophonic Dysplasia | Analgesia | Seborrheic Dermatitis | Vaginitis | Oguchi Disease-2 | Melnick-Needles Syndrome | Early Infantile Epileptic Encephalopathy 1 | Marfan Syndrome | Common Variable Immunodeficiency | Hepatitis, Autoimmune | Gerstmann-Straussler-Scheinker Syndrome | Myositis | Waardenburg Syndrome | Tyrosinemia | Anti-glomerular Basement Membrane Disease | Leukemia | Pontocerebellar Hypoplasia | Ollier Disease | Alopecia | Charcot-Marie-Tooth Disease | Fibromuscular Dysplasia | Methemoglobinemia | Hypersomnia | Chronic Enteropathy Associated With SLCO2A1 Gene | DEND Syndrome | Bronchiolitis | Isovaleric Acidemia | Mitochondrial Encephalomyopathy | DICER1 Syndrome | Hemorrhagic Disorders | Measles | Hemochromatosis | Neurofibroma | Aromatic L-amino Acid Decarboxylase Deficiency | Parvovirus B19 Infection | Angiosarcoma Of The Breast | Familial Thoracic Aortic Aneurysm | Aspartylglycosaminuria | Charcot-Marie-Tooth Disease Type 2D | Multiple Sclerosis | Gastritis | 6-pyruvoyl-tetrahydropterin Synthase Deficiency | Thrombocytopenia | Hypothyroidism | Nestor-Guillermo Progeria Syndrome | Exfoliative Dermatitis | Schwannomatosis | Hypogonadism | GATA2 Deficiency | Bleeding Disorder Due To CalDAG-GEFI Deficiency | Left Ventricular Noncompaction | IgA Deficiency | Facioscapulohumeral Muscular Dystrophy | Pseudohypoparathyroidism Type 2 | Hyper IgE Syndrome | Congenital Lipoid Adrenal Hyperplasia | Autoimmune Hemolytic Anemia | Bullous Pemphigoid | Schwannoma | Cutaneous Mastocytosis | Pseudohypoparathyroidism Type 1A | Epidermolysis Bullosa Acquisita | Urethritis | Mitochondrial DNA Depletion Syndrome, Myopathic Form | Premenstrual Syndrome | Major Depression | Esophageal Carcinoma | Hypertensive Nephropathy | Osteomalacia | Nephropathy | Hypersensitivity Pneumonitis | Platyspondylic Lethal Skeletal Dysplasia, Torrance Type | Cystitis, Interstitial | Brenner Tumor | Shwachman-Bodian-Diamond Syndrome | Myosin Storage Myopathy