Disease

Amyloidosis

About the Disease
Amyloidosis, also known as amyloid disease, is related to amyloidosis, hereditary, transthyretin-related and immunoglobulin light chain amyloidosis. An important gene associated with Amyloidosis is TTR (Transthyretin), and among its related pathways/superpathways are Innate Immune System and Metabolism of proteins. The drugs Citalopram and Ibuprofen have been mentioned in the context of this disorder. Affiliated tissues include brain, heart and kidney, and related phenotypes are no effect and no effect

Common Targets
G596 | CRBN | MFGE8 | PSEN1 | SNCA | TTR | LYZ | ABL1 | G3569 | HDAC6 | LECT2 | CTSS | Matrix Metalloproteinase (MMP) (nonspecified subtype) | NF-kappaB (NFkB) | DHODH | COMT | FERMT2 | G4137 | EIF2AK4 | SAA2-SAA4 | APCS | BACE1 | Amyloid beta A4 precursor protein-binding family (APP-BP) (nonspecified subtype) | DCX (DDB1-CUL4-X-box) E3 protein ligase complex | PDE1B | NPEPPS | MEFV | FPR2 | G836 | GPRC6A | B2M | NR3C1 | TNFRSF17 | APOA1 | GSN | CTSK | CDK8 | EIF2AK3 | OSMR | HPSE | CTSB | APP | SAA1 | Tubulin | G367 | SAA2 | TNFRSF1A | LGALS1 | NLRP12 | G7124 | Proteasome Complex

疾病靶点研报
Amyloidosis

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

Other Diseases

Non-Langerhans Cell Histiocytosis | Retinal Vasculitis | Nestor-Guillermo Progeria Syndrome | Sensory Ataxic Neuropathy, Dysarthria, And Ophthalmoparesis | Achromatopsia | Aicardi-Goutieres Syndrome | Gastrointestinal Disorders | Adenosine Deaminase Deficiency | Retinopathy Of Prematurity | Vasculitis | Porphyria Cutanea Tarda | Non-epidermolytic Palmoplantar Keratoderma | Polymyalgia Rheumatica | Acute Anterior Uveitis | Hypertension, Pulmonary | Progressive Familial Intrahepatic Cholestasis | Primary Carnitine Deficiency | Pompe Disease | Keratoacanthoma | Cold Agglutinin Disease | Cranial Nerve Disease | Cerebellar Ataxia, Cayman Type | Episodic Ataxia Type 2 | Cutaneous Lupus Erythematosus | Chondrosarcoma | Polycythemia Vera | Cholangitis | Mastitis | Arthritis, Gouty | Hyperammonemia | Crohn's Disease | Pantothenate Kinase-associated Neurodegeneration | Basan Syndrome | Astigmatism | Beckwith-Wiedemann Syndrome | Proopiomelanocortin Deficiency | Coenzyme Q10 Deficiency | Non-Hodgkin Lymphoma | Mucolipidosis | Anthrax | Wagner Disease | Paternal Uniparental Disomy Of Chromosome 14 | Muscular Dystrophy | Osteogenesis Imperfecta Type VI | Adenosine Deaminase 2 Deficiency | Multiple Sclerosis | Papilloma | Parapsoriasis | Hemimegalencephaly | Inflammatory Myopathy | Persistent Truncus Arteriosus | Retinitis | Schistosomiasis | Cantu Syndrome | Stuttering | Blue Rubber Bleb Nevus Syndrome | Systemic Lupus Erythematosus | Retinal Detachment | Hypermetropia | Arthritis, Psoriatic | Insulin Resistance | Scabies | Swine Influenza | N-acetylglutamate Synthase Deficiency | Eosinophilic Asthma | Hypertensive Retinopathy | Hyperphosphatasia With Intellectual Disability Syndrome 4 | Obsessive-compulsive Disorder | Unverricht-Lundborg Syndrome | Spasticity | Bulimia Nervosa | Frontotemporal Dementia With Amyotrophic Lateral Sclerosis | Diabetes Insipidus, Nephrogenic | Charcot-Marie-Tooth Disease, Type 1A | Atherosclerosis | Stuve-Wiedemann Syndrome | Meningioma | Dupuytren Disease | Chiari Malformation Type I | Autism Spectrum Disorders | Acute Myeloid Leukemia | Martsolf Syndrome | Bleeding Disorder Due To CalDAG-GEFI Deficiency | Anovulation | Cholestasis | Epidermolysis Bullosa Acquisita | Focal Cortical Dysplasia Type 2 | Waardenburg Syndrome Type 4A | Hartsfield Syndrome | Paraplegia | Pleural Tuberculosis | Dystonia Musculorum Deformans | Preaxial Polydactyly | Nutrition Disorders | Arthritis | Craniosynostosis | Acromicric Dysplasia | Burn-McKeown Syndrome | Osteonecrosis | Meningitis | Urethritis | T-cell Lymphoma, Subcutaneous Panniculitis-like | FG Syndrome | Bronchiectasis | Lymphangiomatosis | Spondylosis | High Molecular Weight Kininogen Deficiency | Macular Degeneration | Diastrophic Dysplasia | Blau Syndrome | Ulcerative Colitis | Oligospermia | Hereditary Coproporphyria | Sclerosteosis | Charcot-Marie-Tooth Disease Type 4 | Osteitis | Muckle-Wells Syndrome | Fetal Akinesia Deformation Sequence | Kashin-Beck Disease | Uterine Leiomyoma | Primary Hyperoxaluria Type 1 | Hydrocephalus | Congestive Heart Failure | Priapism | Snyder-Robinson Syndrome | Pregnancy, Ectopic | Chronic Periodontitis | Aspergillosis | Milk Allergy | Neurodevelopmental Disorder With Central Hypotonia And Dysmorphic Facies | Fatty Aldehyde Dehydrogenase Deficiency | Neurocutaneous Syndromes | Colitis, Microscopic | Tetanus | Charcot-Marie-Tooth Disease Type 2D | Recurrent Respiratory Papillomatosis | Chronic Granulomatous Disease | Pemphigoid | Retinal Degeneration | Long-chain 3-hydroxyacyl-coenzyme A Dehydrogenase Deficiency | Periventricular Nodular Heterotopia | Macular Corneal Dystrophy Type 1 | Panuveitis | Polymyositis | Kidney Stones | Thalassemia | Glanzmann Thrombasthenia | Hereditary Xerocytosis | Charcot-Marie-Tooth Disease | Neutrophilia | Pneumococcal Meningitis | Osteoporosis-pseudoglioma Syndrome | Impetigo | Ichthyosis | 3-hydroxy-3-methylglutaric Aciduria | Acrodysostosis | Hepatic Veno-occlusive Disease | Carney Triad | Myelitis | Sepiapterin Reductase Deficiency | Hemoglobinopathies | Malignant Peripheral Nerve Sheath Tumor | Sporadic Hemiplegic Migraine | Johanson-Blizzard Syndrome | Gastroschisis | Hypogammaglobulinemia | Facioscapulohumeral Muscular Dystrophy | Duodenal Atresia | Woodhouse-Sakati Syndrome | Rubinstein-Taybi Syndrome | Carey-Fineman-Ziter Syndrome | Chorioretinitis | Vitelliform Macular Dystrophy | Enlarged Vestibular Aqueduct | Very Long-chain Acyl-CoA Dehydrogenase Deficiency | Relapsing Polychondritis | Nemaline Myopathy 10 | Chitayat Syndrome | Ghosal Syndrome | Cutaneous T-cell Lymphoma | Metachromatic Leukodystrophy | Congenital Myopathy | Craniofrontonasal Syndrome | Early Infantile Epileptic Encephalopathy 13 | Carcinoma, Merkel Cell | Meningeal Melanocytoma | Amyloidosis | Diabetic Nephropathy | Familial Exudative Vitreoretinopathy | Glioblastoma | Craniopharyngioma | Waardenburg Syndrome Type 4 | Colitis, Collagenous | Peeling Skin Syndrome Type B | Usher Syndrome Type III | Erysipelas | Vitamin K Deficiency | Charcot-Marie-Tooth Disease Type 2E | LRBA Deficiency | Epidermolysis Bullosa Simplex With Mottled Pigmentation | Epicondylitis | Acute Lymphocytic Leukemia | Uremia | Uveitis, Anterior | Tendinopathy | Communication Disorders | Sengers Syndrome | Autosomal Recessive Spastic Paraplegia Type 75 | Mucolipidosis Type IV | Hypercholesterolemia, Familial | Corneal Dystrophy And Perceptive Deafness | Early Infantile Epileptic Encephalopathy 4 | Ichthyosis Hystrix, Curth-Macklin Type | Pain | Hyperparathyroidism | Neurofibrosarcoma | Charcot-Marie-Tooth Disease Axonal Type 2N | Spinal And Bulbar Muscular Atrophy | Nephronophthisis | POEMS Syndrome | Marfan Syndrome | Hepatitis | Hypertrophic Osteoarthropathy, Primary, Autosomal Recessive 2 | Spinocerebellar Ataxia | Hypopigmentation | Costello Syndrome | Citrullinemia | Coma | Psoriasis | Rhinitis | Familial Hemiplegic Migraine | Dyslipidemia | Glomerulonephritis, Membranous | Cryptorchidism | Schistosomiasis Mansoni | Thanatophoric Dysplasia Type 1 | Vitamin A Deficiency | Spitz Nevus | Acrocallosal Syndrome | Purpura, Thrombotic Thrombocytopenic | Membranous Nephropathy | Duane Retraction Syndrome | Intermittent Explosive Disorder | Metatropic Dysplasia | Long QT Syndrome Type 2 | Hepatic Adenomatosis | Persistent Fetal Circulation | Hereditary Multiple Exostoses | Absence Epilepsy | Keratosis | Shwachman-Bodian-Diamond Syndrome | Lymphoma | 3-methylcrotonyl-CoA Carboxylase Deficiency | Silicosis | NGLY1 Deficiency | Fetal And Neonatal Alloimmune Thrombocytopenia | Pancytopenia | Adrenomyeloneuropathy | Pyruvate Carboxylase Deficiency Disease | Infantile Nephropathic Cystinosis | Dementia | Central Retinal Artery Occlusion | Cat Eye Syndrome | Gigantism | Adenomatoid Tumor | Biotinidase Deficiency | Dystonia | Hartnup Disease | Aldosterone Synthase Deficiency | Crimean-Congo Hemorrhagic Fever | Diabetic Macular Edema | Harlequin Ichthyosis | Cluster Headache | Conjunctivitis | Amyotrophic Lateral Sclerosis-parkinsonism-dementia Complex | Rhizomelic Chondrodysplasia Punctata | IMAGe Syndrome | Lung Diseases | Fibromuscular Dysplasia | Viral Meningitis | Charcot-Marie-Tooth Disease, Type 2A | Leukemia-lymphoma, Adult T-cell | Nemaline Myopathy 8 | Chordoma | Gitelman Syndrome | Pearson Syndrome | Krabbe Disease | Impulse Control Disorder | Sleep Apnea, Central | Bardet-Biedl Syndrome | Nevus | Postpoliomyelitis Syndrome | Celiac Disease | Fahr Disease | Fibrillation, Atrial | Schizencephaly | Coloboma | Alexander Disease | Papulopustular Rosacea | Hyper IgE Syndrome | Fontaine Progeroid Syndrome | Double Outlet Right Ventricle | Spinocerebellar Ataxia Type 20 | Esthesioneuroblastoma | Deafness, Dystonia, And Cerebral Hypomyelination | Cancer, Breast | H Syndrome | Nicotine Addiction | Overactive Bladder | Agoraphobia | Pelizaeus-Merzbacher Disease | Rubeosis Iridis | Spinocerebellar Ataxia Type 17 | 3-M Syndrome | Kaposi Sarcoma | Jalili Syndrome | Uremic Pruritus | Scleroderma, Diffuse | Hepatitis B, Chronic | Intestinal Obstruction | Endometritis | Pituitary Stalk Interruption Syndrome | C3 Glomerulopathy | Fibrosis | Tangier Disease | Adult Polyglucosan Body Disease | Steel Syndrome | Angioedema, Acquired | Pulmonary Tuberculosis | Dermatomyositis | Pachyonychia Congenita | Congenital Myasthenic Syndrome | McKusick Type Metaphyseal Chondrodysplasia | Hydronephrosis | Reticular Dysgenesis | Charcot-Marie-Tooth Disease, Type 2C | Presbyopia | Chronic Granulomatous Disease, X-linked | Myopia | Epidermolytic Palmoplantar Keratoderma | Cardiomyopathy, Restrictive | Hennekam Lymphangiectasia-lymphedema Syndrome | Tatton-Brown-Rahman Syndrome | Tonsillitis | Headache | Thrombocythemia, Essential | Primary Hyperoxaluria | Brachydactyly | Chromosome 5q Deletion Syndrome | Hemolytic Uremic Syndrome | Myhre Syndrome | Glycogen Storage Disease Type 0, Muscle | Kohlschutter-Tonz Syndrome | Cockayne Syndrome | Charcot-Marie-Tooth Disease Type 4E | Chondrodysplasia Punctata | Postaxial Polydactyly | Mood Disorder | Optic Nerve Diseases | Distal Myopathy | Erythrokeratodermia Variabilis | Gout | Congenital Hereditary Endothelial Dystrophy Type II | 3-methylglutaconic Aciduria | Lupus Erythematosus | Myasthenia Gravis | Ectopia Lentis, Isolated, Autosomal Recessive | X-linked Myotubular Myopathy | Macrodactyly | Open-angle Glaucoma | Osteogenesis Imperfecta Type I | VACTERL/VATER Association | Gynecomastia | Abetalipoproteinemia | Sclerosteosis 2 | Hypobetalipoproteinemias | Oculocutaneous Albinism Type 1 | Genee-Wiedemann Syndrome | Neovascular Glaucoma | Cenani-Lenz Syndactyly Syndrome | Primary Ovarian Insufficiency | Prader-Willi Syndrome | Proctitis | Familial Pheochromocytoma-paraganglioma | Torticollis | Cryopyrin-associated Periodic Syndromes | Fetal Alcohol Syndrome | Homocystinuria | Ocular Hypertension | Aromatic L-amino Acid Decarboxylase Deficiency | Rheumatoid Arthritis | Porokeratosis | Seizures | Stromal Corneal Dystrophy | Paroxysmal Kinesigenic Dyskinesia | Acromesomelic Dysplasia | Language Disorders | Bullous Pemphigoid | Branchiootorenal Syndrome | Neurofibroma, Plexiform