Disease

Portal Hypertension

About the Disease
Portal Hypertension, also known as hypertension, portal, is related to portal hypertension, noncirrhotic, 2 and hypersplenism, and has symptoms including signs and symptoms, digestive An important gene associated with Portal Hypertension is GIMAP5 (GTPase, IMAP Family Member 5), and among its related pathways/superpathways are Signal Transduction and p70S6K Signaling. The drugs Nitric Oxide and Simvastatin have been mentioned in the context of this disorder. Affiliated tissues include liver, spleen and bone marrow, and related phenotypes are homeostasis/metabolism and growth/size/body region

Common Targets
PNPLA3 | NR3C1 | ROCK1 | DDR2 | GH1 | Somatostatin receptor (nonspecified subtype) | FLT4 | FLT1 | Relaxin receptor (nonspecified subtype) | NOX4 | S1PR2 | KDR | NR1H4 | PDE5A | RAF1 | FLT3 | RET | MBL2 | Prostanoid TP receptor (nonspecified subtype) | SST | Caspase (nonspecified subtype) | HSD17B13 | ROCK2 | CLCN2 | SERPINA1 | NOX1 | MAN1B1 | KIT | Diacylglycerol kinase (nonspecified subtype) | G673 | Soluble guanylyl cyclase | S1PR1 | EDNRA | CD46 | ELANE | AVPR1A | GPBAR1 | LRRK2 | PDGFRB

疾病靶点研报
Portal Hypertension

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

Other Diseases

Cerebrotendinous Xanthomatosis | Leukocyte Adhesion Deficiency | Diabetes | Neurodevelopmental Disorder With Central Hypotonia And Dysmorphic Facies | Anencephaly | Mabry Syndrome | Proopiomelanocortin Deficiency | Waardenburg Syndrome Type 4A | Meier-Gorlin Syndrome | Rosacea | Cranial Nerve Disease | 3-methylglutaconic Aciduria | Autosomal Recessive Spastic Paraplegia Type 54 | Hepatitis C, Chronic | Oral Lichen Planus | Pneumococcal Meningitis | Traboulsi Syndrome | Lattice Corneal Dystrophy Type 1 | ACTH-independent Macronodular Adrenal Hyperplasia | Scapuloperoneal Myopathy, X-linked Dominant | Anorchia | Brooke-Spiegler Syndrome | Tardive Dyskinesia | Astrocytoma | Glycogen Storage Disease Type 6 | Myotonic Disorders | Hyperprolactinemia | Shock, Cardiogenic | Tenosynovial Giant Cell Tumor | Primary Biliary Cholangitis | Vitelliform Macular Dystrophy | Gastric Atrophy | Johanson-Blizzard Syndrome | Pulmonary Alveolar Proteinosis | Myelitis | Rhabdomyosarcoma, Embryonal | Cold Agglutinin Disease | Mast Cell Leukemia | Osteopetrosis | Spinocerebellar Ataxia Type 27 | Cardiomyopathy, Hypertrophic | Facioscapulohumeral Muscular Dystrophy Type 2 | Wolfram Syndrome 2 | Common Variable Immunodeficiency | Sotos Syndrome | Androgen Insensitivity | Graves Disease | Allergic Contact Dermatitis | Phenylketonuria II | Purpura, Thrombotic Thrombocytopenic | Combined Deficiency Of Factor V And Factor VIII | Chronic Neutrophilic Leukemia | Intermittent Explosive Disorder | Chronic Leukemia | Craniometaphyseal Dysplasia | Walker-Warburg Syndrome | Duodenal Atresia | Diabetes Type 2 | Mitochondrial Cytopathy | Niemann-Pick Disease, Type B | Papillorenal Syndrome | Osteosarcoma | Hypotrichosis, Congenital, With Juvenile Macular Dystrophy | Neurodegeneration Due To Cerebral Folate Transport Deficiency | Diabetic Encephalopathy | Hashimoto Thyroiditis | Hoyeraal-Hreidarsson Syndrome | Pelizaeus-Merzbacher Disease | Pyloric Stenosis, Infantile Hypertrophic | NGLY1 Deficiency | Pancytopenia | Bullous Pemphigoid | Hyperparathyroidism | Xeroderma Pigmentosum | Atopy | Primary Cutaneous Amyloidosis | Growth Hormone Excess | Congenital Afibrinogenemia | Polyradiculopathy | Lung Diseases | Myotonia | Polyneuropathy | Argininosuccinic Aciduria | Myelofibrosis | Migraine | Hypertriglyceridemia | Hypercalciuria | Blepharo-cheilo-odontic Syndrome | Basal Ganglia Disease, Biotin-responsive | Syndactyly | Onchocerciasis | Intestinal Tuberculosis | Babesiosis | Granular Corneal Dystrophy Type 1 | Retinal Detachment | Herpes Simplex Dermatitis | Urolithiasis | Proteasome-associated Autoinflammatory Syndrome 2 | Carcinoma, Merkel Cell | Coronary Artery Disease | Noonan Syndrome-like Disorder With Loose Anagen Hair | Primary Sclerosing Cholangitis | DEND Syndrome | Carcinoma, Small Cell | Peeling Skin Syndrome, Acral Type | Discoid Lupus Erythematosus | Apparent Mineralocorticoid Excess Syndrome | Hyperekplexia | Actinomycetoma | Dominant Optic Atrophy | AIDS Dementia Complex | Esthesioneuroblastoma | Nasodigitoacoustic Syndrome | Tendinopathy | Dysequilibrium Syndrome | Tylosis With Esophageal Cancer | Cellulitis | Skin Carcinoma | Persistent Mullerian Duct Syndrome | Pelvic Inflammatory Disease | Raine Syndrome | Split Hand-foot Malformation | Osteogenesis Imperfecta Type VI | Nephropathy | Cornelia De Lange Syndrome | Gardner Syndrome | CEDNIK Syndrome | Osteopathia Striata With Cranial Sclerosis | Keratoacanthoma | Arteriosclerosis | Ameloblastic Carcinoma | Charcot-Marie-Tooth Disease Type 3 | Leprosy | Tuberculosis | Oculopharyngeal Muscular Dystrophy | Cheilitis | Primary Hyperoxaluria | Microvillus Inclusion Disease | Constipation | Pseudoachondroplasia | Hypertrophic Osteoarthropathy, Primary, Autosomal Recessive 2 | Reye Syndrome | Rheumatoid Arthritis | Jacobsen Syndrome | Retinitis Pigmentosa | Antenatal Bartter Syndrome Type 1 | Hyperthyroidism | Presbycusis | Hypotension, Orthostatic | Arthropathy | Cystinuria | Cluster Headache | Zimmermann-Laband Syndrome | Alopecia Totalis | Acute Lung Injury | Hydrops Fetalis | Orotic Aciduria | Hyperostosis | Parkinson Disease 6, Autosomal Recessive Early-onset | Hereditary Folate Malabsorption | Hermansky-Pudlak Syndrome | Congenital Poikiloderma | Hairy Cell Leukemia | Fatty Aldehyde Dehydrogenase Deficiency | Fraser Syndrome | Sclerosing Cholangitis | Pendred Syndrome | Mosaic Variegated Aneuploidy Syndrome 2 | Amblyopia | Primary Hyperoxaluria Type 1 | Paternal Uniparental Disomy Of Chromosome 14 | Pleurisy | Hyperbilirubinemia, Neonatal | Hereditary Hemorrhagic Telangiectasia Type 2 | Epiphyseal Chondrodysplasia, Miura Type | Erythema Nodosum | Polymyositis | Membranous Nephropathy | Endophthalmitis | Sialidosis Type I | Hepatitis B, Chronic | Corneal Edema | Porphyria | Keloid | Blue Nevus | Waldenstrom Macroglobulinemia | Cancer, Bladder | Brugada Syndrome 1 | Dysplastic Nevus | Cancer, Brain | Esophagitis, Eosinophilic | Phenylketonuria | Paronychia | Hepatitis, Alcoholic | Aicardi-Goutieres Syndrome | Chloridorrhea, Congenital | Hemorrhagic Disorders | Cardiac Sarcoidosis | Spastic Paraplegia Type 7 | Multicystic Renal Dysplasia | Chorea-acanthocytosis | Angiomyolipoma | Aromatic L-amino Acid Decarboxylase Deficiency | Li-Fraumeni Syndrome | Alveolar Capillary Dysplasia | Carey-Fineman-Ziter Syndrome | Potocki-Shaffer Syndrome | Eosinophilia | 3-methylcrotonyl-CoA Carboxylase Deficiency | Ocular Surface Squamous Neoplasia | Pouchitis | Lipoma | HIBCH Deficiency | Double Outlet Right Ventricle | GNE Myopathy | Learning Disability | Angiosarcoma | Saethre-Chotzen Syndrome | Episodic Ataxia Type 2 | Iron Overload | Borderline Personality Disorder | Blepharophimosis Syndrome | LRBA Deficiency | Hypersensitivity Pneumonitis | Orthostatic Intolerance | Smoldering Myeloma | Takayasu's Arteritis | Lymphoma, Follicular | Duchenne Muscular Dystrophy | Glutaric Aciduria Type 2 | Acute Tubular Necrosis | Congenital Hereditary Endothelial Dystrophy Type II | Eczema | Sarcoma, Endometrial Stromal | Vascular Calcification | Hyperkeratosis | Personality Disorders | Medulloblastoma | Pierpont Syndrome | Schizophrenia | Anosmia, Congenital | Extramammary Paget's Disease | Mood Disorder | Neurofibrosarcoma | Menetrier Disease | Usher Syndrome Type III | Blomstrand Osteochondrodysplasia | Non-Hodgkin Lymphoma | Photosensitivity | Cataract | Oculocutaneous Albinism | Varices | Conn Syndrome | Keratitis | Myelitis, Transverse | Depression | Diastrophic Dysplasia | Spinal Muscular Atrophy Type 3 | Polycystic Kidney, Autosomal Dominant | Myoclonic Atonic Epilepsy | Hypermetropia | Vertebrobasilar Insufficiency | Primary Erythromelalgia | Unverricht-Lundborg Syndrome | Salla Disease | Chronic Kidney Disease | Auriculocondylar Syndrome | CDKL5 Deficiency Disorder | Acrodermatitis Enteropathica | Temporal Lobe Epilepsy | Fabry's Disease | Encephalitis, Tick-borne | Asthma, Exercise-induced | Hyperglycemia | Mitochondrial DNA Depletion Syndrome, Encephalomyopathic Form | Keratosis, Seborrheic | Diabetes Mellitus, Transient Neonatal | Bacterial Meningitis | Anodontia | Optic Neuritis | Leukodystrophies | Lymphoproliferative Disease, X-linked | Diffuse Mesangial Sclerosis | Neurocutaneous Melanocytosis | Schizotypal Personality Disorder | Angina Pectoris | Martsolf Syndrome | Oligoastrocytoma | Myasthenia Gravis | Gastrointestinal Disorders | Wiskott-Aldrich Syndrome | Robinow Syndrome | Pyruvate Decarboxylase Deficiency | Keratosis, Actinic | Fanconi Anemia | Hydrolethalus Syndrome | Mountain Sickness | Behcet's Disease | Hypokalemic Periodic Paralysis | Aldosterone Deficiency | Castleman Disease | Malignant Fibrous Histiocytoma | Eating Disorder | Adenomyosis | Trigonocephaly | Proctitis | Facioscapulohumeral Muscular Dystrophy Type 1 | Myosin Storage Myopathy | Glutathione Synthetase Deficiency | Exostoses | Hyperbilirubinemia | Rhizomelic Chondrodysplasia Punctata | Macrophage Activation Syndrome | Asthma | Stiff-man Syndrome | Ganglioglioma | Acquired Partial Lipodystrophy | Amyotrophic Lateral Sclerosis, Juvenile | Cryptorchidism | Dyggve-Melchior-Clausen Disease | Fukuyama Congenital Muscular Dystrophy | Overactive Bladder | Leber Congenital Amaurosis | Neurocysticercosis | Dysfibrinogenemia | Epidermolytic Palmoplantar Keratoderma | Hypopigmentation | Alopecia Areata | Hypertension, Portal | Stomatitis | Inborn Errors Of Metabolism | Hypophosphatasia | Trismus-pseudocamptodactyly Syndrome | Long QT Syndrome Type 3 | Precocious Puberty | Van Der Knaap Disease | Prostatitis | Carney Triad | Glycogen Storage Disease Type 5 | Waardenburg Syndrome Type 2A | Cancer, Prostate | Charcot-Marie-Tooth Disease Type 4B1 | Odonto-onycho-dermal Dysplasia | Cushing Syndrome | Pulmonary Tuberculosis | Werner's Syndrome | Light Chain Amyloidosis | Neurofibromatosis Type 2 | Urea Cycle Disorder | Raynaud Phenomenon | 3-M Syndrome | Low Tension Glaucoma | Jalili Syndrome | Goiter | Patent Foramen Ovale | Schizophrenia, Paranoid | Colorectal Adenoma | Temtamy Preaxial Brachydactyly Syndrome | Arthrogryposis | Cardiac Arrest | Eclampsia | Waardenburg Syndrome Type 1 | Partington Syndrome | Keratoconjunctivitis | Twin-to-twin Transfusion Syndrome | 3-hydroxy-3-methylglutaryl-CoA Synthase Deficiency | Spinal And Bulbar Muscular Atrophy | Reticular Dysgenesis | Sleep Apnea, Central | Pituitary Dwarfism | Spasticity | Trachoma | Progressive External Ophthalmoplegia | Autoimmune Interstitial Lung, Joint, And Kidney Disease | Superficial Spreading Melanoma | Thyroid Dyshormonogenesis | Seizures | Uterine Leiomyoma | Adenocarcinoma | Spinocerebellar Ataxia Type 15 | Mitochondrial Myopathy | Focal Facial Dermal Dysplasia | Pulverulent Zonular Cataract | Familial Advanced Sleep Phase Syndrome | Porphyria, Variegate | Anorectal Malformations | Carcinoid Tumor | Aneurysm, Abdominal Aortic | Esophageal Motility Disorders | CHOPS Syndrome | Hydrocephalus, Normal Pressure | Withdrawal Syndrome | Milk Allergy | Rubeosis Iridis | Cutaneous Angiosarcoma | Adult Polyglucosan Body Disease | Methemoglobinemia | Hennekam Lymphangiectasia-lymphedema Syndrome | Central Retinal Artery Occlusion | Lupus Erythematosus