Disease

Cluster Headache

About the Disease
Cluster Headache, also known as headache, cluster, is related to headache and trigeminal neuralgia, and has symptoms including headache and recurrent paroxysmal headache. An important gene associated with Cluster Headache is HCRTR2 (Hypocretin Receptor 2), and among its related pathways/superpathways are Signal Transduction and GPCR downstream signalling. The drugs Zolmitriptan and Ketamine have been mentioned in the context of this disorder. Affiliated tissues include eye, pituitary and brain.

Common Targets
MTERF2 | HTR1A | CNR1 | Alpha-2 Adrenergic receptors (nonspecified subtype) | CRY2 | SLC6A2 | TRPV1 | GH1 | GNB3 | HTR2B | SLC22A3 | SSTR3 | Opioid receptor (nonspecified subtype) | VDR | LOC100507053 | HTR2A | ADH4 | HCRTR2 | Glycogen synthase kinase 3 (GSK-3) (nonspecified subtype) | CALCA | CALCRL | HRH1 | AGTR1 | HTR1B | Muscarinic Acetylcholine Receptor (mAChR) (nonspecified subtype) | 5-Hydroxytryptamine Receptor 2 (5-HT2) (nonspecified subtype) | Cyclooxygenase (COX) (nonspecified subtype) | HTR2C | SSTR5 | Nitric oxide synthase (NOS) (nonspecified subtype) | 5-Hydroxytryptamine Receptor (nonspecified subtype) | SSTR1 | CRY1 | HTR1D | CLOCK | MAPK8IP1 | CNR2 | SSTR2 | HFE

疾病靶点研报
Cluster Headache

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

Other Diseases

Fundus Albipunctatus | Basal Cell Nevus Syndrome | Tangier Disease | Thrombasthenia | Acute Leukemia | Niemann-Pick Disease, Type C | Encephalitis | Pseudohypoparathyroidism Type 1B | Fibrosis | Neuromuscular Disorders | Congenital Hypofibrinogenemia | Hemochromatosis Type 1 | Obesity | Frank-ter Haar Syndrome | Disseminated Superficial Actinic Porokeratosis | Mosaic Variegated Aneuploidy Syndrome 2 | Cold-induced Sweating Syndrome | Turner's Syndrome | Neuroectodermal Tumors, Primitive | Autonomic Neuropathy | Amyloidosis | Spondylolisthesis | Isobutyryl-CoA Dehydrogenase Deficiency | Meckel-Gruber Syndrome | Combined Pituitary Hormone Deficiency | Acrodermatitis | Dent Disease | Duchenne Muscular Dystrophy | Uveitis, Anterior | Primary Aldosteronism | Congenital Myasthenic Syndrome | Subcortical Band Heterotopia | Charcot-Marie-Tooth Disease, Type 2C | Hypertension | Heroin Dependence | Onchocerciasis | Hennekam Lymphangiectasia-lymphedema Syndrome | Unverricht-Lundborg Syndrome | Tibial Muscular Dystrophy | Anorchia | Chronic Myeloid Leukemia | Mitochondrial DNA Depletion Syndrome 13 | Primary Pigmented Nodular Adrenocortical Disease | Lipoma | Erythropoietic Protoporphyria | Genitopatellar Syndrome | Erysipelas | Infantile Neuroaxonal Dystrophy | Pigment Dispersion Syndrome | Dengue Shock Syndrome | Glycogen Storage Disease Type 5 | Orotic Aciduria | Hemorrhagic Disorders | Hypertension, Renovascular | Thyroiditis, Autoimmune | Waardenburg Syndrome | Noonan Syndrome-like Disorder With Loose Anagen Hair | Trimethylaminuria | Sensorineural Hearing Loss | Ollier Disease | Reflex Epilepsy | Glaucoma, Congenital | Graft-versus-host Disease | Renal-hepatic-pancreatic Dysplasia | Microcephalic Osteodysplastic Primordial Dwarfism, Type I | Uremic Pruritus | Familial Isolated Hyperparathyroidism | Dysthymia | Hemorrhoids | Pulmonary Stenosis | Hypophosphatemic Rickets, Autosomal Recessive, 1 | Hypohidrotic Ectodermal Dysplasia | Nephrotic Syndrome Type 1 | Diabetes Insipidus, Nephrogenic | Waardenburg Syndrome Type 4 | Pure Red Cell Aplasia | Waldenstrom Macroglobulinemia | Wolfram Syndrome | Cancer, Lung | Rubinstein-Taybi Syndrome | Mucormycosis | Lymphoma | FG Syndrome | Left Ventricular Noncompaction | Sleep Disorder | Encephalopathy, Ethylmalonic | Pyruvate Carboxylase Deficiency Disease | Lissencephaly 2 | Cabezas Syndrome | Chorioretinitis | Gnathodiaphyseal Dysplasia | Microcephalic Primordial Dwarfism | Lattice Corneal Dystrophy | Congenital Primary Aphakia | Sponastrime Dysplasia | SAPHO Syndrome | Presbyopia | 3-M Syndrome | Congenital Myopathy | Wiskott-Aldrich Syndrome | Atopic Dermatitis | Spinocerebellar Ataxia Type 1 | Rosacea | Leukoplakia | Epilepsy, Generalized | Hypertension, Portal | Pulmonary Sclerosing Hemangioma | Eating Disorder | Premenstrual Syndrome | Congenital Adrenal Hyperplasia 1 | Adenoma, Villous | Molybdenum Cofactor Deficiency | Glycogen Storage Disease Type 3 | Leber Hereditary Optic Neuropathy | Alcoholism | Bloom Syndrome | Glycogen Storage Disease | Kaposi Sarcoma | Chronic Myelomonocytic Leukemia | Hyperbilirubinemia, Neonatal | Paraganglioma, Carotid Body | 3C Syndrome | Diabetes Type 2 | Oculopharyngeal Muscular Dystrophy | Choriocarcinoma | Prurigo Nodularis | Hartnup Disease | Osteomyelitis | Bleeding Disorder Due To CalDAG-GEFI Deficiency | Hypophosphatasia | Fanconi Syndrome | Epidermolytic Palmoplantar Keratoderma | Multiple Congenital Anomalies-hypotonia-seizures Syndrome 2 | Acromicric Dysplasia | Autonomic Nervous System Disorders | Beare-Stevenson Syndrome | Primary Progressive Aphasia | Bacterial Meningitis | Loeys-Dietz Syndrome Type 4 | Paracoccidioidomycosis | Glomerulonephritis, Membranous | Dystonia Musculorum Deformans | Tumoral Calcinosis | B-cell Chronic Lymphocytic Leukemia | Pneumococcal Meningitis | Atrioventricular Septal Defect | Delirium | Charcot-Marie-Tooth Disease, Type 2A | Autosomal Recessive Congenital Ichthyosis | Thalassemia | Still Disease | Vitamin A Deficiency | Renal Tubular Dysgenesis | Chondrodysplasia Punctata | Ectopia Lentis, Isolated, Autosomal Recessive | Ischemia | Jacobsen Syndrome | Chromosome 8q21.11 Deletion Syndrome | Spinal And Bulbar Muscular Atrophy | Joubert Syndrome | Aspartylglycosaminuria | Hartsfield Syndrome | Choreoathetosis, Hypothyroidism, And Neonatal Respiratory Distress | Varicocele | Polycystic Liver | Malignant Peripheral Nerve Sheath Tumor | Myhre Syndrome | Gerstmann-Straussler-Scheinker Syndrome | Diabetes Insipidus, Neurogenic | Behavioral Variant Of Frontotemporal Dementia | Alexander Disease | Primary Familial Brain Calcification | Multiple Sclerosis, Secondary Progressive | Transthyretin-related Amyloidosis | Long-chain 3-hydroxyacyl-coenzyme A Dehydrogenase Deficiency | Congenital Heart Block | Spondyloperipheral Dysplasia | Cancer, Prostate | Hypodontia | Nager Acrofacial Dysostosis | Binge Eating Disorder | Metanephric Adenoma | Keratosis, Actinic | Greenberg Dysplasia | HELLP Syndrome | Bronchiolitis | Schindler Disease | Multiple Epiphyseal Dysplasia | Renal Hypouricemia | Persistent Truncus Arteriosus | Ehlers-Danlos Syndrome | Guttate Psoriasis | Eiken Syndrome | Familial Hemiplegic Migraine | Cri-du-chat Syndrome | Scabies | Desbuquois Syndrome | Lennox-Gastaut Syndrome | Angiosarcoma Of The Breast | Frontometaphyseal Dysplasia | Saul-Wilson Syndrome | Acute Lymphocytic Leukemia | Adrenomyeloneuropathy | Chronic Enteropathy Associated With SLCO2A1 Gene | Smith-Magenis Syndrome | Tenosynovial Giant Cell Tumor | Hyperparathyroidism, Primary | Twin-to-twin Transfusion Syndrome | Spinocerebellar Ataxia Type 15 | Pfeiffer Syndrome | Glycogen Storage Disease Type 1 | Papulopustular Rosacea | Cysticercosis | Juvenile Hyaline Fibromatosis | Delayed Sleep Phase Syndrome | Esotropia | Conn Syndrome | Spinocerebellar Ataxia Type 3 | Congenital Absence Of Vas Deferens | Maple Syrup Urine Disease | Pelizaeus-Merzbacher Disease | Pseudoexfoliation Syndrome | Neuronal Ceroid Lipofuscinosis | Desmosterolosis | Bethlem Myopathy | Tyrosine Hydroxylase Deficiency | Stroke, Hemorrhagic | Hypertrophic Osteoarthropathy, Primary, Autosomal Recessive 2 | Charcot-Marie-Tooth Disease, Type 2 | Hairy Cell Leukemia | Congenital Nephrotic Syndrome | C3 Glomerulonephritis | Schizophrenia, Paranoid | Non-Hodgkin Lymphoma | Dupuytren Disease | Postpoliomyelitis Syndrome | Infertility, Male | Periodic Limb Movement Disorder | Astrocytoma, Anaplastic | Malaria, Cerebral | Diffuse Idiopathic Pulmonary Neuroendocrine Cell Hyperplasia | Proteus Syndrome | Klinefelter Syndrome | Dyggve-Melchior-Clausen Disease | Raynaud Phenomenon | Supravalvular Aortic Stenosis | Glioblastoma | Trichothiodystrophy | Pulmonary Alveolar Microlithiasis | Cholecystitis | Mabry Syndrome | Congenital Generalized Lipodystrophy | Ocular Albinism Type 1 | Cervicitis | Dermatofibrosarcoma | Cannabis Abuse | Urethritis | Sertoli Cell-only Syndrome | 3-hydroxyacyl-CoA Dehydrogenase Deficiency | Aplastic Anemia | Non-small Cell Lung Cancer | Cheilitis | Choroideremia | Hypertrophy | Osteonecrosis | Zollinger-Ellison Syndrome | Goldenhar Syndrome | Trichuriasis | Autoimmune Polyendocrine Syndrome | Tetraplegia | Familial Digital Arthropathy-brachydactyly | Dengue Hemorrhagic Fever | Lymphoma, Mantle Cell | Tuberculosis | Neurofibroma, Plexiform | Prader-Willi Syndrome | Kawasaki Disease | Congenital Ichthyosiform Erythroderma | Aromatic L-amino Acid Decarboxylase Deficiency | Sporadic Inclusion Body Myositis | Purpura | Sensory Neuropathy | Hypoproteinemia, Hypercatabolic | Primary Carnitine Deficiency | Sclerosteosis 2 | Mandibuloacral Dysplasia With Type A Lipodystrophy | MELAS Syndrome | Sick Sinus Syndrome | Diffuse Palmoplantar Keratoderma | Hepatitis | Bone Marrow Necrosis | Van Der Knaap Disease | Microcephalic Osteodysplastic Primordial Dwarfism, Type II | Schwannoma | Gitelman Syndrome | Vitamin D Deficiency | Partington Syndrome | Hypertrophic Osteoarthropathy, Primary, Autosomal Recessive 1 | Ocular Hypertension | Gout | Infantile Liver Failure Syndrome 1 | Retinopathy, Diabetic | Rheumatoid Arthritis | Focal Dermal Hypoplasia | Varices | Persistent Fetal Circulation | Preaxial Polydactyly | Congenital Hereditary Endothelial Dystrophy Type I | Pontocerebellar Hypoplasia | Corneal Edema | Neuroendocrine Cancer | Blepharitis | Ataxia-ocular Apraxia 2 | Kleine-Levin Syndrome | Premature Ejaculation | Hyperacusis | Thin Basement Membrane Disease | Porphyria | Cardiospondylocarpofacial Syndrome | Low Tension Glaucoma | Schwannomatosis | Alpers Syndrome | Retinal Detachment | Diffuse Mesangial Sclerosis | Periventricular Nodular Heterotopia | Synpolydactyly | Haim-Munk Syndrome | Blepharo-cheilo-odontic Syndrome | Epidermolysis Bullosa Dystrophica | Alopecia Areata | Hypertension, Pulmonary | Syndactyly | Hypertensive Retinopathy | Anovulation | Angelman Syndrome | Leber Congenital Amaurosis | Polyradiculopathy | IgA Nephropathy | Adenocarcinoma | Aspergillosis | Optic Neuritis | Primary Sclerosing Cholangitis | Hepatitis D | Melanocytic Nevus | Iron Deficiency Anemia | Nutrition Disorders | Niemann-Pick Disease, Type B | Congenital Torticollis | Sitosterolemia | Wagner Disease | Burn-McKeown Syndrome | Senior-Loken Syndrome | Facioscapulohumeral Muscular Dystrophy Type 1 | Hypotonia-cystinuria Syndrome | Sleep Apnea | Asplenia | Syphilis | Megacystis-microcolon-intestinal Hypoperistalsis Syndrome | Split Hand-foot Malformation | Nicolaides-Baraitser Syndrome | Granular Corneal Dystrophy Type 1 | Duodenal Atresia | Psoriasis | Sjogren Syndrome | Usher Syndrome Type III | Pendred Syndrome | Teratozoospermia | Osteopathia Striata With Cranial Sclerosis | Cardiomyopathy, Restrictive | Osteogenesis Imperfecta Type III | Pneumothorax | Congenital Muscular Dystrophy | Cancer, Breast | Crohn's Disease | Esophageal Carcinoma | Poikiloderma With Neutropenia | Swine Influenza | Long QT Syndrome Type 3 | Hyperuricemia | Pitt-Hopkins Syndrome | Progressive Encephalopathy-optic Atrophy Syndrome | Angina Pectoris | Muscle Wasting | Atelosteogenesis Type 2 | Hemochromatosis Type 2 | Gangliosidosis, GM1 | Pulmonary Veno-occlusive Disease | Coffin-Lowry Syndrome | Congenital Dysfibrinogenemia | Hereditary Spastic Paraplegia | Angiosarcoma | Imerslund-Grasbeck Syndrome | Lymphangioma | Hereditary Hemorrhagic Telangiectasia Type 2 | Branchiootorenal Syndrome | Diffuse Intrinsic Pontine Glioma | Neurogenic Bladder | Hypolipoproteinemia | Granuloma Annulare | Aneurysm, Thoracic Aortic