Stroke, Hemorrhagic

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 Stroke, Hemorrhagic, 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 Stroke, Hemorrhagic at a cost 90% lower than traditional approaches, please feel free to contact us at BD@silexon.tech.

Other Diseases

Adenomatoid Tumor | Acute Tubular Necrosis | Usher Syndrome Type III | Wolman Disease | Congenital Nystagmus | Myelitis | Zimmermann-Laband Syndrome | Lymphedema-distichiasis Syndrome | Teratozoospermia | Charcot-Marie-Tooth Disease Type 4D | Apparent Mineralocorticoid Excess Syndrome | Persistent Truncus Arteriosus | Demyelinating Diseases | Obesity, Morbid | Silicosis | Lymphomatoid Granulomatosis | Chronic Inflammatory Demyelinating Polyneuropathy | Delayed Sleep Phase Syndrome | Thyroid Hormone Resistance | Eating Disorder | Arthritis, Psoriatic | Congenital Dyserythropoietic Anemia | Toxic Epidermal Necrolysis | Paget's Disease Of The Breast | Geleophysic Dysplasia | Pure Autonomic Failure | Fibrodysplasia Ossificans Progressiva | Megacystis-microcolon-intestinal Hypoperistalsis Syndrome | Fetal And Neonatal Alloimmune Thrombocytopenia | Disseminated Intravascular Coagulation | Joubert Syndrome | Dysferlinopathy | Hemorrhagic Disorders | Inflammatory Myopathy | Cutis Laxa | Hoyeraal-Hreidarsson Syndrome | Xeroderma Pigmentosum | Herpes Genitalis | Polyomavirus Nephropathy | Leishmaniasis, Cutaneous | Neural Tube Defect | Cystitis, Interstitial | Motion Sickness | Carotid Artery Disease | Juvenile Myelomonocytic Leukemia | Acne Vulgaris | Skin Carcinoma | Bartter Syndrome | Adenoma, Pleomorphic | Sclerosteosis | Shprintzen-Goldberg Syndrome | Basal Ganglia Disease, Biotin-responsive | Multiple Sulfatase Deficiency | Nemaline Myopathy 8 | Alpha-mannosidosis | Neurodevelopmental Disorders | Blastoma, Pleuropulmonary | Renpenning Syndrome | Fatty Aldehyde Dehydrogenase Deficiency | Chorioretinitis | 3-methylglutaconic Aciduria | Pneumonia, Mycoplasma | Charcot-Marie-Tooth Disease, Type 2C | Crohn's Disease | Dysfibrinogenemia | Peeling Skin Syndrome Type B | Brachydactyly | Schizophrenia, Paranoid | Peyronie's Disease | Diffuse Palmoplantar Keratoderma | Costello Syndrome | Chronic Neutrophilic Leukemia | Dyslipidemia | Cataplexy | Carcinoid Tumor | HUPRA Syndrome | Pityriasis Rubra Pilaris | Ocular Surface Squamous Neoplasia | Osteomalacia | Partington Syndrome | Burn-McKeown Syndrome | Erectile Dysfunction | Carney Triad | Sickle Cell Disease | Tumoral Calcinosis | Thyroid Dyshormonogenesis | Carcinoma In Situ | Vitamin A Deficiency | Dent Disease | Trigonocephaly | Combined Malonic And Methylmalonic Acidemia | Scapuloperoneal Spinal Muscular Atrophy | Haim-Munk Syndrome | Spitz Nevus | Macrophage Activation Syndrome | Melanoma | Tetraplegia | Orotic Aciduria | Japanese Encephalitis | Arthrogryposis | Motor Neuron Diseases | Tylosis With Esophageal Cancer | Coffin-Lowry Syndrome | Odonto-onycho-dermal Dysplasia | Chanarin-Dorfman Syndrome | Hemolytic Uremic Syndrome | Birt-Hogg-Dube Syndrome | Argininosuccinic Aciduria | 6-pyruvoyl-tetrahydropterin Synthase Deficiency | Keratitis | Porencephaly | Agoraphobia | Glycogen Storage Disease Type 0, Muscle | Tonsillitis | Canavan Disease | Bronchiectasis | Chondromyxoid Fibroma | Craniopharyngioma | Astigmatism | Reye Syndrome | Myeloid Leukemia | Kabuki Syndrome 2 | Pneumothorax | Supravalvular Aortic Stenosis | Dementia, Vascular | Smoldering Myeloma | Lymphoproliferative Disorders | Familial Cerebral Amyloid Angiopathy | Loeys-Dietz Syndrome | Retinal Dystrophy | Chronic Thromboembolic Pulmonary Hypertension | Atopy | Lyme Disease | Acute Myeloid Leukemia | Hepatitis, Chronic | Menkes Disease | Congenital Heart Block | Wolff-Parkinson-White Syndrome | Tinea | Progressive Familial Intrahepatic Cholestasis Type 3 | Macrophagic Myofasciitis | Hepatitis C, Chronic | Nephrotic Syndrome Type 1 | Diverticulitis | Allergic Contact Dermatitis | Gerodermia Osteodysplastica | Immunoproliferative Disorders | Pain | Pulmonary Tuberculosis | Rheumatoid Arthritis | Pleurisy | Schizophrenia | Oligoasthenoteratozoospermia | Colitis, Collagenous | Cutaneous Lupus Erythematosus | Chromosome 17q21.31 Deletion Syndrome | Fontaine Progeroid Syndrome | Myasthenia | Ameloblastic Carcinoma | Paraplegia | Nemaline Myopathy | Biotinidase Deficiency | Palsy, Cerebral | Leri Pleonosteosis | Heterotopic Ossification | Mohr-Tranebjaerg Syndrome | LRBA Deficiency | Sarcosinemia | Abetalipoproteinemia | Waardenburg Syndrome | Subacute Sclerosing Panencephalitis | Cardiomyopathy, Dilated, 1L | Basan Syndrome | Intestinal Hypomagnesemia 1 | Familial Hypertrophic Cardiomyopathy | Lattice Corneal Dystrophy Type 1 | Microcephalic Osteodysplastic Primordial Dwarfism, Type I | Alpha-1 Antitrypsin Deficiency | Ventricular Septal Defect | Distal Myopathy | Retinitis Pigmentosa 3 | Placenta Previa | Azoospermia | Lesch-Nyhan Syndrome | Congenital Generalized Lipodystrophy | Epidermal Nevus Syndrome | Multifocal Motor Neuropathy | Acral Lentiginous Melanoma | AIDS Dementia Complex | Juvenile Myoclonic Epilepsy | Muscle Wasting | Osteoporosis | Dystonia | Stiff-man Syndrome | Microcephaly | Adrenoleukodystrophy, X-linked | Trimethylaminuria | Filariasis | Camptocormia | Proopiomelanocortin Deficiency | Epidermolysis Bullosa | Desbuquois Syndrome | Congenital Adrenal Hyperplasia 1 | Myotonia | Hemangioendothelioma | Wolcott-Rallison Syndrome | Osteopetrosis | Arthropathy | Major Depression | Blepharo-cheilo-odontic Syndrome | Obsessive-compulsive Disorder | Sensorineural Hearing Loss | Pseudoachondroplasia | Stroke, Hemorrhagic | Primary Lateral Sclerosis | Spondyloepimetaphyseal Dysplasia With Joint Laxity, Type 3 | Fragile X Syndrome | Coronary Restenosis | Rubinstein-Taybi Syndrome | Hypoproteinemia, Hypercatabolic | Thromboembolism | Meningioma, Benign | Premature Ejaculation | Primrose Syndrome | Mevalonate Kinase Deficiency | DiGeorge Syndrome | Hemochromatosis | Rhabdomyosarcoma, Alveolar | Mandibuloacral Dysplasia With Type A Lipodystrophy | Myotonic Disorders | Oligospermia | Farber Disease | Nicolaides-Baraitser Syndrome | Osteonecrosis | Jawad Syndrome | Angiosarcoma | Hyperinsulinemic Hypoglycemia | Facioscapulohumeral Muscular Dystrophy Type 2 | Uremic Pruritus | Analgesia | Hypersensitivity | Spinocerebellar Ataxia Type 21 | Headache | Heart Septal Defects | Strabismus | Stevens-Johnson Syndrome | Rosacea | Bloom Syndrome | Hyperacusis | Cryoglobulinemia | Primary Progressive Nonfluent Aphasia | Dystrophy, Cone-rod | Renal Oncocytoma | Disseminated Superficial Actinic Porokeratosis | Leiomyoma | Adenoma, Villous | Klippel-Feil Syndrome | Metaphyseal Chondrodysplasia, Schmid Type | Woodhouse-Sakati Syndrome | Melanoma, Malignant | Tatton-Brown-Rahman Syndrome | Smith-Kingsmore Syndrome | Autoimmune Polyendocrine Syndrome | Communication Disorders | Anti-glomerular Basement Membrane Disease | Congenital Stromal Corneal Dystrophy | Von Hippel-Lindau Disease | Ataxia-ocular Apraxia 2 | Interstitial Lung Diseases | Glycogen Storage Disease Type 1b | Charcot-Marie-Tooth Disease, Type 1A | Tic Disorder | Autoimmune Polyendocrinopathy Syndrome Type I | Spinocerebellar Ataxia Type 2 | Hypertrophy | Hennekam Lymphangiectasia-lymphedema Syndrome | Choreoathetosis, Hypothyroidism, And Neonatal Respiratory Distress | Malignant Fibrous Histiocytoma | Acute Lymphocytic Leukemia | Charcot-Marie-Tooth Disease, Type 2 | Choroiditis | Bacterial Meningitis | Ameloblastoma | Schuurs-Hoeijmakers Syndrome | Cellulitis | Diabetic Nephropathy | Lattice Corneal Dystrophy | Perry Syndrome | Neurocutaneous Melanocytosis | Coffin-Siris Syndrome | Cervical Dystonia | Esophagitis | Myhre Syndrome | Waardenburg Syndrome Type 2E | Bernard-Soulier Syndrome | Rhabdoid Tumor | Megalencephaly | Epilepsy | X-linked Acrogigantism | Tyrosinemia Type 2 | Amblyopia | Rett Syndrome | Marfan Syndrome | Crimean-Congo Hemorrhagic Fever | Cryptosporidiosis | Dysgerminoma | Melnick-Needles Syndrome | Premenstrual Syndrome | Wilson's Disease | Agammaglobulinemia | Pierre Robin Syndrome | CEDNIK Syndrome | Gastritis, Atrophic | Pathological Gambling | Epidermolytic Hyperkeratosis | Combined Deficiency Of Factor V And Factor VIII | Arteriosclerosis | Zollinger-Ellison Syndrome | Parkinson Disease 6, Autosomal Recessive Early-onset | Mitochondrial Disease | Paternal Uniparental Disomy Of Chromosome 14 | McLeod Syndrome | GM2-gangliosidosis AB Variant | Tyrosine Hydroxylase Deficiency | Myopia | Apert Syndrome | Cystinuria | Globozoospermia | Polyarteritis Nodosa | Chronic Granulomatous Disease, X-linked | Hyperlipidemia, Familial Combined | Narcolepsy | Familial Hypobetalipoproteinemia | Chondrodysplasia Punctata 1, X-linked Recessive | Hereditary Pyropoikilocytosis | Leigh Syndrome | Charcot-Marie-Tooth Disease Type 2D | Nager Acrofacial Dysostosis | Dysmorphophobia | Primary Aldosteronism | Nestor-Guillermo Progeria Syndrome | Blood Protein Disorders | HIBCH Deficiency | Oligoastrocytoma | Usher Syndrome | Cold-induced Sweating Syndrome | Gastroenteritis | Malnutrition | Nephrotic Syndrome | Kawasaki Disease | Presbycusis | Antisynthetase Syndrome | Infantile Liver Failure Syndrome 1 | Amyotrophic Lateral Sclerosis, Juvenile | Distal Myopathy 2 | Measles | Anemia | Sarcoma, Ewing | Ligneous Conjunctivitis | Intellectual Disability, Autosomal Dominant 5 | Rhizomelic Chondrodysplasia Punctata | Rotor Syndrome | Corneal Dystrophy And Perceptive Deafness | Tularemia | Early Infantile Epileptic Encephalopathy 13 | Hepatorenal Syndrome | Diabetes Insipidus, Nephrogenic | Hemophagocytic Lymphohistiocytosis | Corneal Ulcer | Early Infantile Epileptic Encephalopathy 4 | Guttate Psoriasis | Macular Degeneration | Pineoblastoma | Diabetes Mellitus, Transient Neonatal | Cataract | Metanephric Adenoma | Leukoplakia, Oral | Ichthyosis | Dengue Shock Syndrome | Cold Agglutinin Disease | Cholangiocarcinoma | Diabetes Type 1 | Schizencephaly | Peeling Skin Syndrome, Acral Type | Muir-Torre Syndrome | Thyroiditis | Opisthorchiasis | Amebiasis | Pancytopenia | Ulcerative Colitis | Myositis | Oligodendroglioma | VACTERL/VATER Association | Pemphigoid | Renal Failure | Chondroma | Neuroleptic Malignant Syndrome | Juvenile Xanthogranuloma | Pendred Syndrome | DOCK8 Immunodeficiency Syndrome