Disease

Chronic Thromboembolic Pulmonary Hypertension

About the Disease
Chronic Thromboembolic Pulmonary Hypertension, also known as cteph, is related to pulmonary hypertension and pulmonary hypertension, chronic thromboembolic, without deep vein thrombosis. An important gene associated with Chronic Thromboembolic Pulmonary Hypertension is LINC01094 (Long Intergenic Non-Protein Coding RNA 1094). The drugs Treprostinil and Phylloquinone have been mentioned in the context of this disorder. Affiliated tissues include heart, lung and endothelial, and related phenotypes are congestive heart failure and pulmonary arterial hypertension

Common Targets
PTGIR | CBLN2 | ENG | EDNRB | FGA | SMAD9 | ACVRL1 | KCNK3 | NEDD9 | MAPK10 | Soluble guanylyl cyclase | EDNRA | BMPR2

疾病靶点研报
Chronic Thromboembolic Pulmonary Hypertension

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

Other Diseases

Metaphyseal Chondrodysplasia, Schmid Type | Takayasu's Arteritis | Desbuquois Syndrome | Rhizomelic Chondrodysplasia Punctata | Hypertension | Lentigo | Optic Nerve Diseases | SAPHO Syndrome | Macrophagic Myofasciitis | Epidermolysis Bullosa | Pemphigus | Keratosis, Seborrheic | Carey-Fineman-Ziter Syndrome | Necrobiosis Lipoidica | Scoliosis | Deafness, Dystonia, And Cerebral Hypomyelination | Congenital Dyserythropoietic Anemia Type 1 | AIDS | Diverticulitis | Headache | Spinocerebellar Ataxia Type 7 | Dyggve-Melchior-Clausen Disease | Pierson Syndrome | Coffin-Lowry Syndrome | Cholestasis, Intrahepatic | Oguchi Disease-2 | Spasticity | Costello Syndrome | Hyperacusis | Cholecystitis | Congenital Primary Aphakia | Tularemia | GLUT1 Deficiency Syndrome | Corneal Dystrophy And Perceptive Deafness | Congenital Hypofibrinogenemia | Loeys-Dietz Syndrome Type 4 | Pleurisy | Hereditary Hemorrhagic Telangiectasia Type 2 | Saul-Wilson Syndrome | Schnyder Crystalline Corneal Dystrophy | Seborrheic Dermatitis | Fontaine Progeroid Syndrome | Silicosis | Gingivitis | Hemolytic Anemia | Coffin-Siris Syndrome | Cutaneous Angiosarcoma | Primary Progressive Nonfluent Aphasia | Pituitary Disorders | Uremia | Marfan Syndrome | Swine Influenza | Von Hippel-Lindau Disease | Kashin-Beck Disease | Oculocutaneous Albinism | Pitt-Hopkins Syndrome | Chorioretinitis | Glycogen Storage Disease Type 9 | Diabetes Insipidus, Neurogenic | Autosomal Recessive Spastic Paraplegia Type 75 | Chondrodysplasia Punctata 2, X-linked Dominant | Methemoglobinemia | Malignant Peripheral Nerve Sheath Tumor | Hashimoto Thyroiditis | Succinic Semialdehyde Dehydrogenase Deficiency | Pierre Robin Syndrome | Diabetes Gestational | Agnathia-Otocephaly Complex | Nicotine Addiction | Charcot-Marie-Tooth Disease Type 4D | Ectrodactyly | Orthostatic Intolerance | Syncope | Schnitzler Syndrome | Giant Axonal Neuropathy | Uremic Pruritus | Tyrosinemia | Ovarian Hyperstimulation Syndrome | Cutaneous Lupus Erythematosus | Situs Inversus | Leukodystrophies | Osteogenesis Imperfecta Type II | Diabetes Insipidus | Craniometaphyseal Dysplasia | Leishmaniasis, Visceral | Rothmund-Thomson Syndrome | Trimethylaminuria | Hepatitis, Autoimmune | Combined Deficiency Of Factor V And Factor VIII | Restless Legs Syndrome | Heterotopic Ossification | Hereditary Pyropoikilocytosis | Nutrition Disorders | Adenoma, Pituitary | Hyperostosis | Bursitis | Desmosterolosis | Takenouchi-Kosaki Syndrome | Heart Failure | Cellulitis | Heimler Syndrome | Gaze Palsy, Familial Horizontal, With Progressive Scoliosis, 2 | Uveitis, Anterior | Sitosterolemia | Schwannoma | Mountain Sickness | Canavan Disease | Vici Syndrome | Osteonecrosis | Acquired Partial Lipodystrophy | Angiosarcoma | Coenzyme Q10 Deficiency | Demyelinating Diseases | Histiocytosis | Cholelithiasis | Infantile Spasm | Familial Partial Lipodystrophy | Neuroblastoma | Juvenile Polyposis | Poretti-Boltshauser Syndrome | Meckel-Gruber Syndrome | Chondrodysplasia Punctata 1, X-linked Recessive | Oligoasthenoteratozoospermia | Influenza | Encephalopathy, Ethylmalonic | Blastomycosis | Dermatomyositis | Aldosterone Synthase Deficiency | Chromosome 8q21.11 Deletion Syndrome | Multiple Sulfatase Deficiency | Graft-versus-host Disease | Hartnup Disease | Preaxial Polydactyly | Language Disorders | Hemophagocytic Lymphohistiocytosis | Spinocerebellar Ataxia Type 42 | Cold-induced Sweating Syndrome | L-2-Hydroxyglutaric Aciduria | Dystonia Musculorum Deformans | Hydrolethalus Syndrome | Diabetic Encephalopathy | Spinocerebellar Ataxia Type 2 | Iron Deficiency Anemia | Long QT Syndrome Type 2 | Anorectal Fistula | Thrombophilia | Charcot-Marie-Tooth Disease, Type 2 | Periventricular Nodular Heterotopia | Adrenoleukodystrophy, X-linked | Early Infantile Epileptic Encephalopathy | Sarcoidosis | Tylosis With Esophageal Cancer | Hyperoxaluria | Ganglioglioma | Mandibuloacral Dysplasia With Type A Lipodystrophy | Aplasia Cutis Congenita | Neuronal Ceroid Lipofuscinosis | Narcolepsy | Protein C Deficiency | Pulverulent Zonular Cataract | Pulmonary Capillary Hemangiomatosis | Paget's Disease Of The Breast | Pyelonephritis | Dysplastic Nevus | Mohr-Tranebjaerg Syndrome | Autoimmune Disease | Polyneuropathy | Congenital Adrenal Hyperplasia 1 | Fanconi Syndrome | Progressive Osseous Heteroplasia | Generalized Epilepsy With Febrile Seizures Plus | Cardiac Sarcoidosis | Bartsocas-Papas Syndrome | Adenoma, Pleomorphic | Lymphopenia | Analgesia | Thyroid Dysgenesis | Erythema Multiforme | Pompe Disease | Allergic Contact Dermatitis | Strabismus | Chronic Myeloid Leukemia | Adenocarcinoma | Waardenburg Syndrome | Epidermolysis Bullosa Simplex With Mottled Pigmentation | Wiedemann-Steiner Syndrome | Gerodermia Osteodysplastica | Kaposi Sarcoma | Hidradenitis | Pituitary Dwarfism | Sleep Apnea | Harlequin Ichthyosis | Pyloric Stenosis, Infantile Hypertrophic | Carcinoid Syndrome | Macular Corneal Dystrophy Type 1 | Rolandic Epilepsy | Lipid Metabolism Disorders | Alpha-thalassemia Myelodysplasia Syndrome | Inflammatory Bowel Disease | Glycogen Storage Disease Type 5 | Urolithiasis | Carney-Stratakis Syndrome | 3-hydroxy-3-methylglutaryl-CoA Synthase Deficiency | Opisthorchiasis | Neuroma | Cheilitis | Steel Syndrome | Hypohidrotic Ectodermal Dysplasia, X-linked | Menkes Disease | Hypersensitivity | Pyruvate Kinase Deficiency | Intellectual Disability, Autosomal Dominant 5 | Retinal Vasculitis | Chondrosarcoma | Cornelia De Lange Syndrome | Megacystis-microcolon-intestinal Hypoperistalsis Syndrome | Shprintzen-Goldberg Syndrome | Impulse Control Disorder | Corneal Dystrophies, Hereditary | Geleophysic Dysplasia | Congenital Ichthyosiform Erythroderma | Rotor Syndrome | Essential Fructosuria | Cancer, Lung | Bruck Syndrome | Corneal Edema | Acromesomelic Dysplasia | Anuria | Zellweger Syndrome | Whipple's Disease | Craniosynostosis | Stickler Syndrome | Papulopustular Rosacea | Pycnodysostosis | Spinocerebellar Ataxia Type 10 | Angioimmunoblastic T-cell Lymphoma | Primary Pigmented Nodular Adrenocortical Disease | Lymphoma | Raine Syndrome | N-acetylglutamate Synthase Deficiency | CHOPS Syndrome | Cardiac Arrest | Hemolytic Uremic Syndrome, Atypical | Spermatocele | Neurofibrosarcoma | Episodic Ataxia | Cryptosporidiosis | LEOPARD Syndrome | Acute Chest Syndrome | Open-angle Glaucoma | Pneumonia, Mycoplasma | Echinococcosis | Delayed Sleep Phase Syndrome | Encephalitis | Dominant Optic Atrophy | Uterine Leiomyoma | Anorectal Malformations | Primary Hyperoxaluria Type 1 | Distal Myopathy | Hereditary Sensory And Autonomic Neuropathy | Fibromyalgia | Botulism | Nephrotic Syndrome Type 1 | Cutaneous Mastocytosis | Cryoglobulinemia | Chronic Inflammatory Demyelinating Polyneuropathy | Lymphoma, Mantle Cell | Noonan Syndrome-like Disorder With Loose Anagen Hair | Focal Cortical Dysplasia Type 2 | Loeys-Dietz Syndrome | Congenital Bile Acid Synthesis Defect | Sclerocornea | Disseminated Superficial Actinic Porokeratosis | Limb Girdle Muscular Dystrophy | Dent Disease | Esophageal Carcinoma | Insulin Resistance | Peutz-Jeghers Syndrome | Spitz Nevus | Peripheral T-cell Lymphoma | Proteasome-associated Autoinflammatory Syndrome 2 | Pulmonary Veno-occlusive Disease | Rickets | Phenylketonuria II | Progressive Familial Intrahepatic Cholestasis Type 2 | Pulmonary Alveolar Proteinosis | Alstrom Syndrome | Mucolipidosis Type II | Meleda Disease | Idiopathic Multicentric Castleman Disease | Localized Scleroderma | Brachydactyly | Lichen Sclerosus | Subacute Sclerosing Panencephalitis | Keratocystic Odontogenic Tumor | Temporal Lobe Epilepsy | Syphilis | Choroideremia | Scleritis | Schistosomiasis | Oculopharyngeal Muscular Dystrophy | Niemann-Pick Disease | Hyperekplexia | Aromatic L-amino Acid Decarboxylase Deficiency | Parkinson Disease 6, Autosomal Recessive Early-onset | Osteosarcoma | Blomstrand Osteochondrodysplasia | Takotsubo Cardiomyopathy | Leukocyte Adhesion Deficiency | Autosomal Recessive Spastic Paraplegia Type 54 | Ganglioneuroma | Dwarfism | Astigmatism | Personality Disorders | Down Syndrome | Diabetic Neuropathy | Diabetes Type 1 | Pulmonary Alveolar Microlithiasis | Spondylosis | Twin-to-twin Transfusion Syndrome | Poikiloderma With Neutropenia | Temtamy Preaxial Brachydactyly Syndrome | Pneumothorax | Glucagonoma | Hyperuricemic Nephropathy, Familial Juvenile | Otopalatodigital Syndrome Type 2 | Erythrokeratodermia Variabilis | CDKL5 Deficiency Disorder | Lymphoma, AIDS-related | Currarino Syndrome | Sponastrime Dysplasia | Schwannomatosis | Chiari Malformation Type I | Myoclonic Epilepsy With Ragged Red Fibers | Intestinal Hypomagnesemia 1 | Colitis, Microscopic | Arthritis, Psoriatic | Contact Dermatitis | Chorea | Aicardi-Goutieres Syndrome | Cancer, Prostate | Blepharospasm | Uveitis | Angiomyolipoma | Neonatal Progeroid Syndrome | Macrodactyly | Microcephalic Osteodysplastic Primordial Dwarfism, Type I | Alopecia Totalis | Oculocutaneous Albinism Type 4 | Heart Block | Methylmalonic Acidemia | Branchiootorenal Syndrome | Thin Basement Membrane Disease | Spina Bifida | MELAS Syndrome | Bicuspid Aortic Valve | Neural Tube Defect | Cryopyrin-associated Periodic Syndromes | Porencephaly | Brenner Tumor | Joubert Syndrome 2 | Oral Lichen Planus | Kallmann Syndrome | Supravalvular Aortic Stenosis | Mitochondrial DNA Depletion Syndrome 13 | Smith-Kingsmore Syndrome | Adult Polyglucosan Body Disease | X-linked Creatine Transporter Deficiency | Glioblastoma Multiforme | Pulmonary Tuberculosis | Crouzon Syndrome With Acanthosis Nigricans | Danon Disease | Inflammatory Linear Verrucous Epidermal Nevus | Ellis-Van Creveld Syndrome | Bronchiectasis | Primary Cutaneous Amyloidosis | Huntington's Disease-like 2 | Osteogenesis Imperfecta Type VI | Isobutyryl-CoA Dehydrogenase Deficiency | Fetal And Neonatal Alloimmune Thrombocytopenia | Nasodigitoacoustic Syndrome | Acute Lung Injury | Antithrombin III Deficiency | Benign Familial Pemphigus | Dysfibrinogenemia | Endocarditis | X-linked Sideroblastic Anemia | Peroxisomal Disorder | Snyder-Robinson Syndrome | Chronic Idiopathic Myelofibrosis | Riboflavin Transporter Deficiency Neuronopathy | Sezary Syndrome | Spinal Muscular Atrophy Type 3 | Alpers Syndrome | Dysferlinopathy | Hypophosphatemic Rickets, Autosomal Recessive, 1 | Hyperkalemic Periodic Paralysis | Multiple Epiphyseal Dysplasia | Epidermolysis Bullosa Acquisita | Charcot-Marie-Tooth Disease Type 3