Hemorrhagic Stroke

About the Disease
Hemorrhage, Intracerebral, also known as intracerebral hemorrhage, is related to cerebral amyloid angiopathy, app-related and porencephaly, and has symptoms including angina pectoris, back pain and chest pain. An important gene associated with Hemorrhage, Intracerebral is ACE (Angiotensin I Converting Enzyme), and among its related pathways/superpathways are Signaling by Receptor Tyrosine Kinases and Regulation of Insulin-like Growth Factor (IGF) transport and uptake by Insulin-like Growth Factor Binding Proteins (IGFBPs). The drugs Progesterone and Warfarin have been mentioned in the context of this disorder. Affiliated tissues include brain, cortex and heart, and related phenotypes are growth/size/body region and nervous system

Common Targets
DCC | COL3A1 | ALOX15 | MTHFR | HMOX1 | TBXAS1 | SELE | Proteasome Complex | G6647 | EDNRA | m-Calpain | GHRL | SCN10A | TTR | Vascular endothelial growth factors (VEGF) (nonspecified subtype) | G7124 | Phosphodiesterase 1 (PDE1) (nonspecified subtype) | DGAT2 | Phospholipase A2 (nonspecified subtype) | ALOX12 | CIRBP | IGFBP1 | SIGMAR1 | G3479 | ACE | G842 | PPARA | KEAP1 | ESR2 | PGAM5-KEAP1-NRF2 Complex | CD14 | G4780 | NF-kappaB (NFkB) | ABCA1 | G7852 | IGFBP3 | G7099 | 15-Lipoxygenase (nonspecified subtype) | G142 | Amyloid beta A4 precursor protein-binding family (APP-BP) (nonspecified subtype) | CYP4A22 | Heme Oxygenase (HO) (nonspecified subtype) | OPRD1 | SERPINE1 | PPARG | G3480 | SST | S1PR5 | TLR2 | ITGB3 | G4318 | CDK5RAP3 | MC4R | LTC4S | APP | NMDA receptor | PARP2 | NT5E | MMP2 | KRR1 | CRP | HTR2A | BIRC5 | LTA4H | LY96 | NOS2 | RIPK1 | S1PR1 | APOE | FGF2 | CAPN2

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

Other Diseases

Wilson's Disease | Anuria | Adams-Oliver Syndrome | Withdrawal Syndrome | Globozoospermia | Pericarditis | Gaucher Disease | Conn Syndrome | Intestinal Obstruction | Optic Neuropathy, Anterior Ischemic | Hypotrichosis | Blepharo-cheilo-odontic Syndrome | Crigler-Najjar Syndrome | Large Granular Lymphocytic Leukemia | Central Retinal Artery Occlusion | Tendinopathy | Epidermolytic Hyperkeratosis | Pfeiffer Syndrome | Schaaf-Yang Syndrome | Chromosome 16p11.2 Deletion Syndrome | Peritonitis | Spinal Muscular Atrophy With Progressive Myoclonic Epilepsy | Klippel-Feil Syndrome | Benign Hereditary Chorea | Pierre Robin Syndrome | Cysticercosis | Sick Sinus Syndrome | Rolandic Epilepsy | Avian Influenza | Neurofibroma | Pneumonia, Mycoplasma | Cheilitis | Bone Marrow Necrosis | Lymphoma, Follicular | Glomerulonephritis | Epilepsy Of Infancy With Migrating Focal Seizures | Ornithine Transcarbamylase Deficiency | Sarcoidosis | Renal Oncocytoma | Congenital Adrenal Hyperplasia 1 | Neuronal Ceroid Lipofuscinosis | Histiocytic Sarcoma | Facioscapulohumeral Muscular Dystrophy Type 2 | Menkes Disease | Meningioma | Bronchiolitis | X-linked Acrogigantism | Ichthyosis | Carotid Artery Disease | Pontocerebellar Hypoplasia | Bulimia Nervosa | Pulmonary Capillary Hemangiomatosis | Amebiasis | Ventricular Septal Defect | Charcot-Marie-Tooth Disease Type 4D | GLUT1 Deficiency Syndrome | Angina Pectoris | Osteomalacia | Congenital Dyserythropoietic Anemia | Glomerulonephritis, Membranoproliferative | Carcinoma, Merkel Cell | Biotinidase Deficiency | Cushing Syndrome | Dystrophy, Cone-rod | Emery-Dreifuss Muscular Dystrophy | Retinitis Pigmentosa | Chronic Mucocutaneous Candidiasis | Leiomyoma | Congenital Ichthyosiform Erythroderma | Stiff-man Syndrome | Juvenile Myoclonic Epilepsy | Melanocytic Nevus | Pemphigus | Porphyria, Variegate | DNA Ligase IV Deficiency | Thanatophoric Dysplasia Type 1 | Pterygium | Leri-Weill Dyschondrosteosis | Kohlschutter-Tonz Syndrome | Generalized Epilepsy And Paroxysmal Dyskinesia | Aphasia | Eczema | Fanconi Syndrome | Cold-induced Sweating Syndrome | DEND Syndrome | Chitayat Syndrome | Angiomyolipoma | Thalassemia, Beta | Sponastrime Dysplasia | Retinitis | Stromal Corneal Dystrophy | Sarcoma, Endometrial Stromal | Cholera | Generalized Epilepsy With Febrile Seizures Plus | Stomatitis | Holt-Oram Syndrome | KBG Syndrome | Maternally Inherited Diabetes And Deafness | Bartter Syndrome | Congenital Diaphragmatic Hernia | Progressive Familial Intrahepatic Cholestasis Type 2 | Congenital Tufting Enteropathy | Corneal Edema | Familial Glucocorticoid Deficiency | Antenatal Bartter Syndrome Type 1 | Sporadic Hemiplegic Migraine | Wolff-Parkinson-White Syndrome | Stuve-Wiedemann Syndrome | Dyslexia | Tyrosinemia Type 2 | Fibronectin Glomerulopathy | Liebenberg Syndrome | Fibrosis | Eosinophilic Asthma | Netherton Syndrome | LMNA-related Congenital Muscular Dystrophy | Pilomatrix Carcinoma | Congenital Mirror Movements | Hyperammonemia | Dwarfism | Dermatitis Herpetiformis | Hereditary Hemorrhagic Telangiectasia Type 2 | Hyperphenylalaninemia | Primrose Syndrome | Lymphoma | Malignant Peripheral Nerve Sheath Tumor | Blepharoconjunctivitis | Intellectual Disability, Autosomal Dominant 5 | Fibromyalgia | Spondyloarthritis | Congenital Myopathy | Ataxia-hypogonadism-choroidal Dystrophy Syndrome | Cryoglobulinemia | Blepharophimosis Syndrome | Placenta Previa | Analgesia | Cholangiocarcinoma | Acne Vulgaris | Alexander Disease | Paget's Disease Of The Breast | Familial Pheochromocytoma-paraganglioma | Arthritis | Myelomeningocele | Pleural Tuberculosis | Myelitis | Mucormycosis | Johanson-Blizzard Syndrome | Tyrosinemia | Contact Dermatitis | Gangliosidosis | Astrocytoma, Anaplastic | Neurofibroma, Plexiform | Kashin-Beck Disease | Porphyria | Hereditary Multiple Exostoses | Mitochondrial DNA Depletion Syndrome, Hepatocerebral Form | Chronic Granulomatous Disease | Perivascular Epithelioid Cell Tumor | Microtia | Bladder Exstrophy | Leukoencephalopathy, Progressive Multifocal | Apraxia | Polymyalgia Rheumatica | Pearson Syndrome | Apparent Mineralocorticoid Excess Syndrome | Pendred Syndrome | Congenital Afibrinogenemia | Hypercholesterolemia | Primary Pigmented Nodular Adrenocortical Disease | Brachydactyly | Neuroectodermal Tumors, Primitive | Duodenal Atresia | GATA2 Deficiency | Dengue Hemorrhagic Fever | Donnai-Barrow Syndrome | Fibromuscular Dysplasia | Urea Cycle Disorder | Oculocutaneous Albinism Type 4 | Early Infantile Epileptic Encephalopathy 1 | Renal Tubular Dysgenesis | Gestational Trophoblastic Disease | Dowling-Degos Disease | Acute Lymphocytic Leukemia | Acute Leukemia | Thrombophilia | Thrombosis | Cerebral Amyloid Angiopathy | Cluster Headache | Supravalvular Aortic Stenosis | Corneal Dystrophy | Adenomatoid Tumor | Plasmacytoma | Distal Spinal Muscular Atrophy | Inflammatory Myofibroblastic Tumor | Spinocerebellar Ataxia Type 3 | Benign Familial Pemphigus | Small Lymphocytic Lymphoma | Craniosynostosis | Cavitary Optic Disc Anomalies | Waardenburg Syndrome Type 4A | Lichen Sclerosus | Vitreoretinopathy, Proliferative | Neurogenic Bladder | Chronic Kidney Disease | Polydactyly | Gray Platelet Syndrome | Anemia | Preaxial Polydactyly | Congenital Primary Aphakia | Renpenning Syndrome | Agnathia-Otocephaly Complex | Osteogenesis Imperfecta Type III | T-cell Prolymphocytic Leukemia | Cyclic Vomiting Syndrome | Woodhouse-Sakati Syndrome | Basal Ganglia Disease | Asthma | Eating Disorder | Granular Corneal Dystrophy Type 1 | Stroke, Ischemic | Angiosarcoma Of The Breast | Hyperglycemia | Glycogen Storage Disease Type 6 | Succinic Semialdehyde Dehydrogenase Deficiency | Brenner Tumor | Diabetes Mellitus, Transient Neonatal | Congenital Bile Acid Synthesis Defect | Seizures | Von Willebrand Disease | Lymphopenia | Angioedema, Hereditary | IMAGe Syndrome | Aneurysm, Thoracic Aortic | Tyrosinemia Type 1 | Otopalatodigital Syndrome Type 2 | Osteosclerosis | Marfan Syndrome | Osteogenesis Imperfecta Type VI | Vasculitis | Multiple Myeloma | Congenital Absence Of Vas Deferens | Hyperlipidemia Type V | Coloboma | Esotropia | Greenberg Dysplasia | Cockayne Syndrome | Arterial Tortuosity Syndrome | Thyroid Dyshormonogenesis | Choroiditis | Paraganglioma | Vascular Calcification | Epidermodysplasia Verruciformis | Hyperlipidemia, Familial Combined | Spondylosis | Primary Ovarian Insufficiency | Infantile Liver Failure Syndrome 1 | Tardive Dyskinesia | Pituitary Dwarfism | Polyradiculopathy | Glycogen Storage Disease Type 1 | Spondylocostal Dysostosis | Epithelioid Hemangioma | Acromicric Dysplasia | Macular Corneal Dystrophy | Hyperprolactinemia | Methylmalonic Aciduria And Homocystinuria, CblC Type | Trichotillomania | Systemic Lupus Erythematosus | Vertebrobasilar Insufficiency | Chordoid Glioma | HIBCH Deficiency | Hepatitis E | Myoclonus-dystonia Syndrome | Neuroendocrine Cancer | Guttate Psoriasis | Hyperparathyroidism, Primary | Oculocutaneous Albinism | Hypertension, Pulmonary | Ameloblastoma | Obesity, Morbid | Prediabetes | Progressive Encephalopathy-optic Atrophy Syndrome | Zygomycosis | Myocardial Infarction | Endometriosis | Neutrophilia | Usher Syndrome Type IIC | Loeys-Dietz Syndrome | Urofacial Syndrome | Esophageal Adenocarcinoma | Cyst | Varices | Camptocormia | Mitochondrial Cytopathy | Leber Hereditary Optic Neuropathy | Periventricular Leukomalacia | Rhinitis | Premenstrual Syndrome | Transient Bullous Dermolysis Of The Newborn | Long-chain 3-hydroxyacyl-coenzyme A Dehydrogenase Deficiency | Rhizomelic Chondrodysplasia Punctata | Arthritis, Psoriatic | Mitochondrial DNA Depletion Syndrome | Hypersensitivity | Congenital Heart Defects | Primary Erythromelalgia | Cystitis | Blau Syndrome | Nicotine Dependence | Granular Corneal Dystrophy | Hypohidrotic Ectodermal Dysplasia | Rothmund-Thomson Syndrome | Spondyloepimetaphyseal Dysplasia With Joint Laxity, Type 3 | Porencephaly | Clouston Hidrotic Ectodermal Dysplasia | Glycogen Storage Disease Type 3 | Neurodermatitis | Vogt-Koyanagi-Harada Syndrome | Infertility | Overactive Bladder | Reye Syndrome | Sleep Disorder | Retinal Detachment | Moyamoya Disease | Mesothelioma, Malignant | Rosacea | Cardiomyopathy, Peripartum | Keratoacanthoma | Danon Disease | Babesiosis | Spondyloepiphyseal Dysplasia Tarda, X-linked | Camurati-Engelmann Disease | Lissencephaly 2 | Diabetes Insipidus | Hyperkeratosis | Hypotonia-cystinuria Syndrome | Wolfram Syndrome | Hereditary Sensory And Autonomic Neuropathy | HUPRA Syndrome | Charcot-Marie-Tooth Disease, Type 1A | Niemann-Pick Disease | Open-angle Glaucoma | Congenital Dyserythropoietic Anemia Type 4 | Charcot-Marie-Tooth Disease, Type 6 | Leber Congenital Amaurosis | Tatton-Brown-Rahman Syndrome | Epidermolysis Bullosa Simplex, Generalized | Kleine-Levin Syndrome | Filariasis | Adenoid Cystic Carcinoma | Primary Torsion Dystonia | Anthrax | Amyotrophic Lateral Sclerosis, Juvenile | Frontometaphyseal Dysplasia | Lassa Fever | Familial Advanced Sleep Phase Syndrome | Krabbe Disease | Muscle Wasting | Epidermolysis Bullosa Simplex, Localized | Renal Hypomagnesemia 3 | Pulmonary Sclerosing Hemangioma | Esophageal Motility Disorders | Oligospermia | Retinal Coloboma | Acute Myeloid Leukemia | Amish Infantile Epilepsy Syndrome | Pure Autonomic Failure | Currarino Syndrome | Creutzfeldt-Jakob Disease | Congenital Dysfibrinogenemia | Tonsillitis | Arts Syndrome | Thrombotic Microangiopathy | Agranulocytosis | Choriocarcinoma | Episodic Ataxia | Ichthyosis, X-linked | Ligneous Conjunctivitis | DiGeorge Syndrome | Obesity | Ataxia-ocular Apraxia 2 | Trichuriasis | Hyperlipidemia | 17-beta-hydroxysteroid Dehydrogenase X Deficiency | Anorchia | Familial Partial Lipodystrophy | Shprintzen-Goldberg Syndrome | Chondrodysplasia Punctata 1, X-linked Recessive | Lymphangioleiomyomatosis | Cancer, Bladder | Mohr-Tranebjaerg Syndrome | Neuropathy | Motion Sickness | Bronchitis | Bone Giant Cell Tumor | Ichthyosis Hystrix, Curth-Macklin Type | Lymphoma, Primary Cutaneous Anaplastic Large Cell | Progressive External Ophthalmoplegia | Hyperparathyroidism | Methylmalonic Acidemia