Disease

Cerebral Amyloid Angiopathy

About the Disease
Cerebral Amyloid Angiopathy, Cst3-Related, also known as cerebral amyloid angiopathy, is related to cerebral amyloid angiopathy, app-related and gerstmann-straussler disease. An important gene associated with Cerebral Amyloid Angiopathy, Cst3-Related is CST3 (Cystatin C), and among its related pathways/superpathways are Alzheimer's disease and miRNA effects and Presenilin-Mediated Signaling. The drugs Phenol and Acetylsalicylic acid have been mentioned in the context of this disorder. Affiliated tissues include brain, cortex and spleen, and related phenotypes are stroke and cerebral hemorrhage

Common Targets
TARDBP | CHRNA7 | beta-Secretase (nonspecified subtype) | Chaperone (nonspecified subtype) | PTK2B | Amyloid beta A4 precursor protein-binding family (APP-BP) (nonspecified subtype) | APOE | BACE1 | CR1 | APP | NT5E | ACE | NR1D1 | MTHFR | SNCA | CST3 | TTR | gamma-Secretase

疾病靶点研报
Cerebral Amyloid Angiopathy

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

Other Diseases

Nephritis, Interstitial | Osteogenesis Imperfecta Type IV | Melnick-Needles Syndrome | Familial Hyperaldosteronism | Myocarditis | Hyperekplexia | Charcot-Marie-Tooth Disease Type 2E | Hernia, Inguinal | Corneal Dystrophy | Cousin Syndrome | Sengers Syndrome | Hyperhomocysteinemia | Focal Segmental Glomerulosclerosis | Language Disorders | Unverricht-Lundborg Syndrome | Connective Tissue Disorders | Hypothalamic Obesity | Antenatal Bartter Syndrome Type 1 | Patent Foramen Ovale | Ichthyosis Bullosa Of Siemens | Carey-Fineman-Ziter Syndrome | Nance-Horan Syndrome | Myotonic Disorders | Congenital Absence Of Vas Deferens | Chronic Idiopathic Myelofibrosis | Schistosomiasis | Agammaglobulinemia | Kabuki Syndrome 2 | Epidermolytic Palmoplantar Keratoderma | Inflammatory Bowel Disease | Endocarditis | Learning Disability | Chronic Beryllium Disease | Autonomic Nervous System Disorders | Proximal Symphalangism | Ectodermal Dysplasia | Poretti-Boltshauser Syndrome | Castleman Disease | Neurodegeneration With Brain Iron Accumulation | Triple A Syndrome | Glioblastoma | Spinocerebellar Ataxia Type 6 | Osteoporosis | Focal Dermal Hypoplasia | Restless Legs Syndrome | Plasmacytoma | Stroke | Optic Neuritis | Exocrine Pancreatic Insufficiency | Lymphoproliferative Disorders | Endophthalmitis | Cutaneous Angiosarcoma | Amblyopia | Pompe Disease | Ichthyosis, X-linked | Autoimmune Disease | Genitopatellar Syndrome | Sarcoma, Endometrial Stromal | Congenital Afibrinogenemia | Paraganglioma, Carotid Body | Rickets | Hypersensitivity Pneumonitis | Hypoglycemia | Frontotemporal Dementia With Amyotrophic Lateral Sclerosis | Spondyloepiphyseal Dysplasia Tarda, X-linked | Turner's Syndrome | Gastrointestinal Disorders | Blau Syndrome | Charcot-Marie-Tooth Disease, Type 2A | Pulmonary Sclerosing Hemangioma | Omenn Syndrome | Fontaine Progeroid Syndrome | Congenital Bile Acid Synthesis Defect | Primary Erythromelalgia | Ataxia-hypogonadism-choroidal Dystrophy Syndrome | Behcet's Disease | Porphyria Cutanea Tarda | Dermatofibrosarcoma | Multiple System Atrophy | Schnitzler Syndrome | AIDS | Pseudomyxoma Peritonei | Shock, Cardiogenic | Periodic Limb Movement Disorder | Acute Anterior Uveitis | Epidermolytic Hyperkeratosis | Early Infantile Epileptic Encephalopathy 13 | Richter's Syndrome | Kohlschutter-Tonz Syndrome | Common Cold | Cardiac Arrest | Histiocytosis | Lipodystrophy | Agnathia-Otocephaly Complex | Sensory Neuropathy | Mastitis | H Syndrome | Alazami Syndrome | Acute Generalized Exanthematous Pustulosis | Oculocutaneous Albinism Type 4 | Allergic Contact Dermatitis | Bacterial Meningitis | Hypotrichosis | Neurocutaneous Melanocytosis | Vitiligo | Colitis, Lymphocytic | Cystitis, Interstitial | Cerebral Cavernous Malformations | Crouzon Syndrome With Acanthosis Nigricans | Sickle Cell Disease | Metachromatic Leukodystrophy | Tuberculosis | Congenital Torticollis | Ophthalmoplegia | Takotsubo Cardiomyopathy | Dystonia Musculorum Deformans | Micropenis | Aspartylglycosaminuria | L-2-Hydroxyglutaric Aciduria | Myoclonus-dystonia Syndrome | Vascular Calcification | Insulin Resistance | VEXAS Syndrome | Apparent Mineralocorticoid Excess Syndrome | Congenital Muscular Dystrophy | Hyperlipidemia | Charcot-Marie-Tooth Disease Type 3 | Charcot-Marie-Tooth Disease Axonal Type 2N | Diabetes Mellitus, Transient Neonatal | Glycogen Storage Disease Type 3 | Swine Influenza | Sclerosteosis | Anxiety Disorders | Majeed Syndrome | Nanophthalmos | Cholangitis | Saul-Wilson Syndrome | Tardive Dyskinesia | Very Long-chain Acyl-CoA Dehydrogenase Deficiency | Hyperphosphatasia With Intellectual Disability Syndrome 4 | Keratocystic Odontogenic Tumor | Asphyxia Neonatorum | Hypertension, Renal | Carpenter Syndrome | Neuroectodermal Tumors, Primitive | Multiple Sclerosis | Cataplexy | Metabolic Syndrome | Crisponi Syndrome | Danon Disease | Vogt-Koyanagi-Harada Syndrome | Dysferlinopathy | Xeroderma Pigmentosum | Joubert Syndrome | Gnathodiaphyseal Dysplasia | Pyruvate Dehydrogenase Deficiency | Hypertension, Essential | SAPHO Syndrome | Panuveitis | C3 Glomerulopathy | Brooke-Spiegler Syndrome | Gilbert Syndrome | Papulopustular Rosacea | Postpoliomyelitis Syndrome | Pneumothorax | Bethlem Myopathy | Chronic Neutrophilic Leukemia | Contact Dermatitis | Congenital Hereditary Endothelial Dystrophy Type II | Lymphangioleiomyomatosis | Basan Syndrome | Maternally Inherited Diabetes And Deafness | Cenani-Lenz Syndactyly Syndrome | Pyoderma Gangrenosum | Polycystic Liver | Aldosterone Synthase Deficiency | Progressive External Ophthalmoplegia | Necrotizing Autoimmune Myopathy | Choreoathetosis, Hypothyroidism, And Neonatal Respiratory Distress | Scabies | Hypomyelination With Atrophy Of Basal Ganglia And Cerebellum | Coma | Cri-du-chat Syndrome | Spinocerebellar Ataxia Type 1 | Renal Tubular Dysgenesis | Sleep Apnea, Central | Raynaud Phenomenon | Macular Degeneration | TARP Syndrome | Multiple Hamartoma Syndrome | Mabry Syndrome | Cholecystitis | Schizencephaly | Ataxia-ocular Apraxia 2 | Martsolf Syndrome | Menetrier Disease | Osteochondroma | Schistosomiasis Mansoni | Cat Eye Syndrome | Burn-McKeown Syndrome | Cryoglobulinemia | Bronchiolitis | Ghosal Syndrome | Nephrotic Syndrome | Usher Syndrome Type II | Camurati-Engelmann Disease | Hypophosphatasia | Asplenia | Thanatophoric Dysplasia Type 1 | Borderline Personality Disorder | Angiosarcoma Of The Breast | Hydrolethalus Syndrome | Choroideremia | Renal Tubular Acidosis | Fetal Akinesia Deformation Sequence | Gigantism | Pfeiffer Syndrome | Dermatomyositis | Small Lymphocytic Lymphoma | Leri Pleonosteosis | Angiodysplasia | Myoclonic Atonic Epilepsy | Raine Syndrome | Cystinuria | Pseudo-pseudohypoparathyroidism | Steel Syndrome | Macrophagic Myofasciitis | Multiple Myeloma | Vasculitis | Varicocele | Opisthorchiasis | Arthritis, Reactive | Wolff-Parkinson-White Syndrome | Twin-to-twin Transfusion Syndrome | Congenital Dyserythropoietic Anemia Type 1 | Syphilis | Hypertension | Wagner Disease | Chorea | Spinocerebellar Ataxia Type 8 | ICF Syndrome | Pulmonary Vein Stenosis | Eosinophilia | Keratopathy | Frank-ter Haar Syndrome | Pulmonary Alveolar Proteinosis | Rheumatoid Arthritis | Large Granular Lymphocytic Leukemia | Angioedema, Acquired | Snyder-Robinson Syndrome | Epilepsy, Generalized | Thrombophlebitis | Pituitary Disorders | Cholelithiasis | Dupuytren Disease | Necrobiosis Lipoidica | Diabetic Neuropathy | Hyperbilirubinemia, Neonatal | Scoliosis | Inflammatory Linear Verrucous Epidermal Nevus | Urea Cycle Disorder | Spondylo-ocular Syndrome | Bone Marrow Necrosis | Fukuyama Congenital Muscular Dystrophy | Binge Eating Disorder | Dentinogenesis Imperfecta | Erythrokeratodermia Variabilis | Localized Scleroderma | Primary Biliary Cholangitis | Palmoplantar Keratoderma | Zellweger Syndrome | Colitis, Collagenous | Erythromelalgia | Diabetes Insipidus, Nephrogenic | Overactive Bladder | 3-hydroxyacyl-CoA Dehydrogenase Deficiency | Medium-chain Acyl-CoA Dehydrogenase Deficiency | Rotor Syndrome | Nicotine Addiction | Salla Disease | Alpha-thalassemia Myelodysplasia Syndrome | Astrocytoma, Anaplastic | Vascular Cognitive Impairment | N-acetylglutamate Synthase Deficiency | Hypertrophic Osteoarthropathy, Primary, Autosomal Recessive 1 | Gangliosidosis, GM1 | Personality Disorders | Pseudohermaphroditism | Spinocerebellar Ataxia Type 20 | Nager Acrofacial Dysostosis | Pupil Disorders | Retinal Degeneration | Aldosteronism | Smith-Lemli-Opitz Syndrome | Thrombotic Microangiopathy | Charcot-Marie-Tooth Disease Type 4B1 | Phosphoenolpyruvate Carboxykinase Deficiency, Cytosolic | Partington Syndrome | Adenoma, Pituitary | Bipolar Disorder | Basal Ganglia Cerebrovascular Disease | Chordoid Glioma | Nail-Patella Syndrome | Vertebrobasilar Insufficiency | Obesity, Morbid | Alcoholism | Chronic Lymphocytic Leukemia | Parvovirus B19 Infection | Intermittent Explosive Disorder | Waardenburg Syndrome | Herpes Simplex Dermatitis | Lymphoproliferative Disease, X-linked | Kaposiform Hemangioendothelioma | Jawad Syndrome | Multiple Mitochondrial Dysfunctions Syndrome Type 1 | Protein C Deficiency | Brugada Syndrome 1 | Silicosis | Bicuspid Aortic Valve | Lissencephaly 2 | Hyperkeratosis | Cholesteryl Ester Storage Disease | Hemophilia | Erysipelas | Lymphopenia | Tricho-hepato-enteric Syndrome | Meckel-Gruber Syndrome | 3-M Syndrome | Lattice Corneal Dystrophy Type 1 | Hepatitis A | Hyperammonemia | Cherubism | Retinitis | Hepatic Veno-occlusive Disease | Stevens-Johnson Syndrome | Pituitary Dwarfism | Transient Bullous Dermolysis Of The Newborn | Myelitis | Corneal Edema | Apert Syndrome | Hereditary Coproporphyria | Carcinoid Syndrome | Schizophrenia, Paranoid | Leishmaniasis, Visceral | Relapsing Polychondritis | Congenital Bilateral Absence Of Vas Deferens | Congenital Nephrotic Syndrome | Distal Myopathy | Woodhouse-Sakati Syndrome | Weill-Marchesani Syndrome | Leukodystrophies | Lafora Disease | Dyskeratosis Congenita | Adenomatoid Tumor | Leber Hereditary Optic Neuropathy | Fanconi Anemia | VACTERL/VATER Association | Epidermal Nevus Syndrome | Paraganglioma | Hemochromatosis Type 1 | Eczema | Cataract | Antley-Bixler Syndrome | Eccrine Porocarcinoma | Periventricular Nodular Heterotopia | Hyperkalemic Periodic Paralysis | Osteogenesis Imperfecta Type V | Abetalipoproteinemia | Acute Tubular Necrosis | Hyperinsulinism-hyperammonemia Syndrome | Epithelioid Hemangioma | Frontotemporal Dementia | Tietze Syndrome | Peritonitis | Osteosarcoma | Yellow Fever | Liver Failure | Uveitis | Thrombasthenia | Neurofibromatosis Type 2 | Cardiospondylocarpofacial Syndrome | Pneumonia, Viral | Osteomyelitis | Presbyopia | Panic Disorder | Autosomal Recessive Spastic Paraplegia Type 35 | Cockayne Syndrome | Wolfram Syndrome | Chromosome 5q Deletion Syndrome | Periodontitis | Erdheim-Chester Disease | Pyruvate Kinase Deficiency | Methemoglobinemia Type IV | Megaloblastic Anemia | Hydrocephalus, Normal Pressure | Keratitis-ichthyosis-deafness Syndrome | Hypercalciuria | Anemia | Bronchitis | Congenital Ichthyosiform Erythroderma