Hemorrhage
Hemorrhage
About the Disease
Bleeding Disorder, Platelet-Type, 11, also known as glycoprotein vi deficiency, is related to thrombocytopenic purpura, autoimmune and purpura, and has symptoms including abdominal pain, angina pectoris and chest pain. An important gene associated with Bleeding Disorder, Platelet-Type, 11 is GP6 (Glycoprotein VI Platelet), and among its related pathways/superpathways are Signal Transduction and Response to elevated platelet cytosolic Ca2+. The drugs Probucol and Glycerin have been mentioned in the context of this disorder. Affiliated tissues include brain, placenta and whole blood, and related phenotypes are epistaxis and bruising susceptibility
Common Targets
CYP2C19 | gamma-Secretase | VWF | F9 | BMP4 | MAOA | COMT | ITGA2 | GATA1 | G23411 | VKORC1 | MC2R | ESAM | PDGFD | NR1I2 | G3630 | AKR1B1 | F10 | XDH | OXT | G5243 | SELP | MTHFR | F2 | CES1 | SERPINE1 | NOS3 | G1956 | PLG | PLAT | MMP2 | CYP3A5 | FASN | STS | JAM3 | PDE5A | Serine protease (nonspecified subtype) | F5 | ORM1 | CYP2J2 | PKM | CFTR | GGCX | CYP2C9 | PON1 | SLCO1B1 | JAK2 | ITGB3 | OR4D2 | PRR5L | APOE | F2RL3 | HNF4A | GP6 | CYP4F2 | F11 | APOB | KLKB1 | LOC101927314 | EPHX1 | G472 | Arginase (nonspecified subtype) | NQO1 | F2R | OXTR | F7 | Voltage-Gated Calcium Channel alpha-2/delta (nonspecified subtype) | DDAH2 | EPHA7 | LPA | FGG | SCN5A | TGFB1 | PRKG1 | PTGFR | DPYD | Vasopressin V1 Receptor (nonspecified subtype) | THBD | LTF | GALNT14 | AMP-activated protein kinase (AMPK) | F8 | Fibrinogen | ACE

Note: If you'd like to get a target analysis report for Hemorrhage, 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 Hemorrhage at a cost 90% lower than traditional approaches, please feel free to contact us at BD@silexon.tech.
Other Diseases
Early Infantile Epileptic Encephalopathy 28 | Oligodendroglioma | Charcot-Marie-Tooth Disease Type 3 | Narcolepsy | Infertility | Spondylocostal Dysostosis | Meconium Ileus | Uremia | Congenital Stromal Corneal Dystrophy | Myofibromatosis | Carcinoma, Squamous Cell | Huntington's Disease | Lassa Fever | Poretti-Boltshauser Syndrome | Histiocytosis | Hypohidrotic Ectodermal Dysplasia, X-linked | Pregnancy, Ectopic | Panic Disorder | Corneal Dystrophy | Multifocal Motor Neuropathy | Borjeson-Forssman-Lehmann Syndrome | Gray Platelet Syndrome | Hypodontia | Macular Degeneration | Autosomal Recessive Congenital Ichthyosis | Pleurisy | Guillain-Barre Syndrome | Spitzoid Melanoma | Nephrocalcinosis | Tibial Muscular Dystrophy | Japanese Encephalitis | Hereditary Coproporphyria | X-linked Myotubular Myopathy | Uveitis | Cri-du-chat Syndrome | Hypertrophy | Anti-glomerular Basement Membrane Disease | Sarcosinemia | Ovarian Sex Cord-stromal Tumor | Saethre-Chotzen Syndrome | Infertility, Male | Genitopatellar Syndrome | Retinal Degeneration | Goldenhar Syndrome | Zollinger-Ellison Syndrome | Haim-Munk Syndrome | Benign Familial Neonatal Convulsions | Episodic Ataxia Type 2 | Thanatophoric Dysplasia Type 1 | Stargardt Disease | Craniofrontonasal Syndrome | Pycnodysostosis | CHOPS Syndrome | Mitochondrial DNA Depletion Syndrome | Homocystinuria | Hereditary Neuropathy With Liability To Pressure Palsies | Meier-Gorlin Syndrome | Smith-Kingsmore Syndrome | Leukoplakia | Neutrophilia | Gingivitis | Duane Retraction Syndrome | Sick Sinus Syndrome 1 | Neuroleptic Malignant Syndrome | Galactosemia | Hypermethioninemia | Autoimmune Polyendocrine Syndrome | Alpha-thalassemia Myelodysplasia Syndrome | Chronic Lymphocytic Leukemia | Angiodysplasia | Carbamoyl Phosphate Synthetase I Deficiency | Neuroendocrine Cancer | Prolactinoma | Costello Syndrome | Dysthymia | ICF Syndrome | Trachoma | Bronchitis, Chronic | Nephrosclerosis | Liver Failure, Acute Infantile | Parkinsonism | Gangliosidosis | Fukuyama Congenital Muscular Dystrophy | Proctitis | Episodic Ataxia Type 1 | Pyruvate Dehydrogenase Deficiency | Fibromuscular Dysplasia | Rett Syndrome | Fuchs Heterochromic Iridocyclitis | Arthritis, Gouty | Seborrheic Dermatitis | Chromosome 16p11.2 Deletion Syndrome | Paraganglioma | Ataxia-ocular Apraxia 2 | Cardiomyopathy, Hypertrophic | Zygomycosis | Toxic Epidermal Necrolysis | DICER1 Syndrome | Ileitis | Mycosis Fungoides | Epidermodysplasia Verruciformis | Deafness, Dystonia, And Cerebral Hypomyelination | Hypoplastic Left Heart Syndrome | Niemann-Pick Disease, Type C | Adenocarcinoma | Amebiasis | Pseudo-pseudohypoparathyroidism | Brenner Tumor | Aneurysm, Abdominal Aortic | Gynecomastia | Lactose Intolerance | Osteochondrosis | Kashin-Beck Disease | Encephalitis | Alexander Disease | Hidradenitis | Mitochondrial DNA Depletion Syndrome, Encephalomyopathic Form | Klinefelter Syndrome | Heart Block | Hemorrhage | Chronic Inflammatory Demyelinating Polyneuropathy | Encephalopathy, Ethylmalonic | Multiple Sclerosis, Primary Progressive | Takotsubo Cardiomyopathy | Diabetic Encephalopathy | Viral Meningitis | Erythema Nodosum | Senior-Loken Syndrome | Exfoliative Dermatitis | Mitochondrial DNA Depletion Syndrome 13 | Microcephaly, Seizures, And Developmental Delay | Netherton Syndrome | Diabetes | Acrocallosal Syndrome | Blue Nevus | Neurodevelopmental Disorder With Central Hypotonia And Dysmorphic Facies | Mucolipidosis Type IV | Emery-Dreifuss Muscular Dystrophy | Tuberculous Meningitis | Charcot-Marie-Tooth Disease Type 2D | Intestinal Hypomagnesemia 1 | Peyronie's Disease | Non-Langerhans Cell Histiocytosis | Panuveitis | Tay-Sachs Disease | Congestive Heart Failure | Primary Progressive Nonfluent Aphasia | Macular Corneal Dystrophy | Metachondromatosis | Tuberculosis | Skin Fragility-woolly Hair Syndrome | T-cell Leukemia | Actinomycetoma | Crouzon Syndrome With Acanthosis Nigricans | Pouchitis | Juvenile Hyaline Fibromatosis | Porphyria Cutanea Tarda | Urolithiasis | Sepiapterin Reductase Deficiency | Melnick-Needles Syndrome | McLeod Syndrome | Primary Familial Brain Calcification | Neuroma | Papillon-Lefevre Syndrome | Neuropathy | Myelitis, Transverse | Enterocolitis, Necrotizing | Dystonia-parkinsonism, X-linked | Achromatopsia | Primary Ovarian Insufficiency | Agoraphobia | Mitochondrial DNA Depletion Syndrome, Hepatocerebral Form | Giant Cell Arteritis | Anal Fissure | Cole-Carpenter Syndrome | Withdrawal Syndrome | Jacobsen Syndrome | Chronic Enteropathy Associated With SLCO2A1 Gene | Hypersensitivity Pneumonitis | Spondylocarpotarsal Synostosis Syndrome | GAPO Syndrome | Thrombocythemia, Essential | Lymphangioleiomyomatosis | Trichuriasis | Neurodevelopmental Disorders | Keratoconus | Esophagitis | Acromesomelic Dysplasia | Brooke-Spiegler Syndrome | Glanzmann Thrombasthenia | Pemphigus | Diabetes Type 2 | Maternally Inherited Diabetes And Deafness | Hepatitis E | Methemoglobinemia Type IV | Glomerulonephritis | Ophthalmoplegia | Neural Tube Defect | Conjunctivitis | Astigmatism | Portal Vein Thrombosis | Chediak-Higashi Syndrome | Short-chain Acyl-CoA Dehydrogenase Deficiency | Isobutyryl-CoA Dehydrogenase Deficiency | Eosinophilic Asthma | Poirier-Bienvenu Neurodevelopmental Syndrome | Achondrogenesis | Optic Neuritis | Alopecia | Glomerulonephritis, Membranoproliferative | Wolcott-Rallison Syndrome | Growth Hormone Excess | Erythropoietic Protoporphyria | Autism | Hyperlipidemia Type V | Milk Allergy | Bulimia Nervosa | Neurogenic Bladder | Sporadic Hemiplegic Migraine | Encephalopathy | Glutaric Aciduria Type 2 | Anodontia | Hypopigmentation | Primary Lateral Sclerosis | Asthma | Granuloma Annulare | Pigment Dispersion Syndrome | Colorectal Adenoma | Diabetes Insipidus | Large Granular Lymphocytic Leukemia | Mandibuloacral Dysplasia With Type A Lipodystrophy | Thrombocytopenia | Hyperlipidemia | Lymphangiomatosis | Charcot-Marie-Tooth Disease Type 2T | Donnai-Barrow Syndrome | Atelosteogenesis Type 2 | Antley-Bixler Syndrome | Waardenburg Syndrome Type 1 | Pneumonia, Viral | Pelizaeus-Merzbacher Disease | T-cell Chronic Lymphocytic Leukemia | Craniolenticulosutural Dysplasia | PHARC Syndrome | Eclampsia | Autoimmune Hemolytic Anemia | Renal Oncocytoma | Colitis, Collagenous | Tenosynovial Giant Cell Tumor | Glaucoma, Congenital | Xeroderma Pigmentosum Variant Type | Malaria, Cerebral | Primary Torsion Dystonia | Bartsocas-Papas Syndrome | Liddle Syndrome | Atrioventricular Septal Defect | Joubert Syndrome 2 | KBG Syndrome | Myelofibrosis | Congenital Dyserythropoietic Anemia Type 4 | Cholecystitis | Woodhouse-Sakati Syndrome | Frank-ter Haar Syndrome | Cystinosis | Craniometaphyseal Dysplasia | Congenital Dyserythropoietic Anemia | Adrenoleukodystrophy, X-linked | Hepatitis C, Chronic | Lymphoma, Primary Cutaneous Anaplastic Large Cell | Ichthyosis Bullosa Of Siemens | Spinal Muscular Atrophy With Progressive Myoclonic Epilepsy | Basal Ganglia Cerebrovascular Disease | Erysipelas | Distal Myopathy | Hepatic Veno-occlusive Disease | Sarcoma | Rickets | Ornithine Transcarbamylase Deficiency | Osteosarcoma | Chronic Granulomatous Disease, X-linked | Down Syndrome | Delirium | Dermatitis Herpetiformis | Lennox-Gastaut Syndrome | GLUT1 Deficiency Syndrome | Schizotypal Personality Disorder | Posterior Polar Cataract | Microcephalic Osteodysplastic Primordial Dwarfism, Type I | Spina Bifida | Aplasia Cutis Congenita | McKusick Type Metaphyseal Chondrodysplasia | Patent Foramen Ovale | Spondylo-ocular Syndrome | Neurocutaneous Syndromes | Chromosome 5q Deletion Syndrome | Cholelithiasis | Glioma | Spinocerebellar Ataxia Type 20 | Glycogen Storage Disease Type 0, Muscle | Infantile Liver Failure Syndrome 1 | Hypertension, Portal | Diverticulitis | Postpoliomyelitis Syndrome | Persistent Truncus Arteriosus | Hyperkeratosis | Erectile Dysfunction | Spinocerebellar Ataxia Type 10 | Interstitial Lung Diseases | Delayed Sleep Phase Syndrome | Gastrointestinal Disorders | Carcinoma In Situ | Erythromelalgia | Bethlem Myopathy | Multiple Sclerosis, Relapsing-remitting | Osteochondroma | Beare-Stevenson Syndrome | Spinocerebellar Ataxia Type 17 | Crohn's Disease | Motion Sickness | Greig Cephalopolysyndactyly Syndrome | Ischemia | Myhre Syndrome | Lathosterolosis | Left Ventricular Noncompaction | Glaucoma | Tinea Versicolor | Epidermal Nevus Syndrome | Torticollis | Multicentric Carpotarsal Osteolysis Syndrome | Cryptococcal Meningitis | Pancreatitis, Chronic | Lymphoma, Mantle Cell | Blepharophimosis Syndrome | Von Hippel-Lindau Disease | Olmsted Syndrome | Raine Syndrome | Motor Neuron Diseases | Non-Hodgkin Lymphoma | Neuromuscular Disorders | Hyperostosis | Spitz Nevus | Ophthalmia, Sympathetic | Anosmia, Congenital | Dwarfism | Iron Deficiency Anemia | Muckle-Wells Syndrome | Glycogen Storage Disease Type 1a | Rhizomelic Chondrodysplasia Punctata | Lewy Body Dementia | Blepharoconjunctivitis | Apert Syndrome | Hyperammonemia | Hyperbilirubinemia, Neonatal | Liver Failure | Amelanotic Melanoma | Bruck Syndrome | Cocaine-Related Disorders | Birk-Barel Syndrome | Contact Dermatitis | Renpenning Syndrome | Juvenile Myelomonocytic Leukemia | Alzheimer Disease, Late Onset | Cockayne Syndrome | Leiomyoma | Triple A Syndrome | Tonsillitis | Cholestasis | X-linked Charcot-Marie-Tooth Disease | Ocular Albinism Type 1 | Coffin-Lowry Syndrome | Glycogen Storage Disease Type 3 | Nijmegen Breakage Syndrome | Stroke, Ischemic | Cerebral Cavernous Malformations | Sleep Disorder | Eczema | Chronic Periodontitis | Graft-versus-host Disease | Osteogenesis Imperfecta Type II | Language Disorders | Autosomal Recessive Spastic Paraplegia Type 75 | Hemochromatosis Type 1 | Dent Disease | Obesity | Hypoparathyroidism | Obesity, Morbid | Nevus | Pseudohypoparathyroidism Type 1B | Allan-Herndon-Dudley Syndrome | Progressive Familial Intrahepatic Cholestasis | Renal Hypomagnesemia 3 | Primary Progressive Aphasia | Ligneous Conjunctivitis | Chronic Leukemia | Dysferlinopathy | Polycythemia | Kaposiform Hemangioendothelioma | Leukoplakia, Oral | Hodgkin Lymphoma | Parkinson's Disease