Disease

Loeys-Dietz Syndrome

About the Disease
Loeys-Dietz Syndrome, also known as loeys-dietz aortic aneurysm syndrome, is related to loeys-dietz syndrome 1 and loeys-dietz syndrome 2. An important gene associated with Loeys-Dietz Syndrome is TGFBR2 (Transforming Growth Factor Beta Receptor 2), and among its related pathways/superpathways are Signal Transduction and ERK Signaling. The drugs Heparin, bovine and Liver Extracts have been mentioned in the context of this disorder. Affiliated tissues include spinal cord, bone and skin, and related phenotypes are high palate and pes planus

Common Targets
TGFBR1 | SMAD2 | TGFB2 | SMAD3 | TGFBR2 | TGFB3 | IPO8 | FBN1

疾病靶点研报
Loeys-Dietz Syndrome

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

Other Diseases

Citrullinemia | Neuroectodermal Tumors, Primitive | Kindler Syndrome | Epidermal Nevus Syndrome | Prediabetes | Osteitis | Sleep Apnea, Obstructive | Monilethrix | Anovulation | Spinocerebellar Ataxia Type 5 | Polydactyly | Dermatofibrosarcoma | Optic Neuritis | Hypertelorism | Gilbert Syndrome | Inflammatory Bowel Disease | Dyslipidemia | Malaria | Arthrogryposis | Mitochondrial DNA Depletion Syndrome | Noonan Syndrome | Hyperhomocysteinemia | Lymphedema-distichiasis Syndrome | Schistosomiasis Mansoni | Mixed Connective Tissue Disease | Polycystic Kidney, Autosomal Recessive | Hyperbilirubinemia | Lissencephaly 2 | Diffuse Mesangial Sclerosis | Waardenburg Syndrome Type 2E | Diamond-Blackfan Anemia | Plasma Cell Dyscrasia | Split Hand-foot Malformation | Infantile Neuroaxonal Dystrophy | Thrombasthenia | CHOPS Syndrome | Maternally Inherited Diabetes And Deafness | Frank-ter Haar Syndrome | Enlarged Vestibular Aqueduct | Chediak-Higashi Syndrome | Cancer, Brain | Spinocerebellar Ataxia Type 38 | Creutzfeldt-Jakob Disease | Frontotemporal Dementia With Amyotrophic Lateral Sclerosis | Albinism | Congestive Heart Failure | Spondyloepiphyseal Dysplasia Tarda, X-linked | PASLI Disease | Vascular Cognitive Impairment | Conjunctivitis, Allergic | Anti-NMDA Receptor Encephalitis | Spinal Muscular Atrophy With Progressive Myoclonic Epilepsy | Hartnup Disease | Corneal Ulcer | Vitamin A Deficiency | Burn-McKeown Syndrome | Macrophagic Myofasciitis | Bone Marrow Necrosis | Glutaric Aciduria Type 3 | Congenital Central Hypoventilation Syndrome | Spinocerebellar Ataxia Type 15 | Lassa Fever | Actinomycetoma | Thrombophlebitis | Macular Corneal Dystrophy Type 1 | Hypogammaglobulinemia | Familial Mediterranean Fever | Hepatitis | Kallmann Syndrome | Still Disease | Spitzoid Melanoma | Spinocerebellar Ataxia Type 3 | Dwarfism | Papilledema | Localized Scleroderma | GNE Myopathy | Juvenile Myoclonic Epilepsy | 3-hydroxyacyl-CoA Dehydrogenase Deficiency | Progressive Encephalopathy-optic Atrophy Syndrome | Hypertension, Renovascular | Sotos Syndrome | Transthyretin-related Amyloidosis | Stromal Corneal Dystrophy | Paternal Uniparental Disomy Of Chromosome 14 | Esophagitis | Familial Isolated Hyperparathyroidism | Cavitary Optic Disc Anomalies | Acute Kidney Injury | Adenomyosis | Chronic Granulomatous Disease, X-linked | Porphyria, Variegate | Cerebral Cavernous Malformations | Hemorrhage | Aarskog-Scott Syndrome | Disseminated Superficial Actinic Porokeratosis | Bulimia Nervosa | Hemolytic Uremic Syndrome | Marinesco-Sjogren Syndrome | Thrombotic Microangiopathy | Danon Disease | Dystonia-parkinsonism, X-linked | Light Chain Amyloidosis | Colorectal Adenoma | Seizures-scoliosis-macrocephaly Syndrome | Parkinson's Disease | Sclerosing Cholangitis | Alstrom Syndrome | Intracerebral Hemorrhage | Myopia | Myopathy | Primary Lateral Sclerosis | Necrobiosis Lipoidica | Dystonia | Idiopathic Multicentric Castleman Disease | Orotic Aciduria | Stroke, Hemorrhagic | Mitochondrial DNA Depletion Syndrome, Encephalomyopathic Form | Schizophrenia | Neurocutaneous Melanocytosis | Paget's Disease Of The Breast | Anorectal Fistula | Absence Epilepsy | Interstitial Lung Diseases | Craniosynostosis | Hidradenitis | Traboulsi Syndrome | Corneal Dystrophies, Hereditary | Spinocerebellar Ataxia Type 2 | Cryopyrin-associated Periodic Syndromes | Sclerosteosis 2 | Hypophosphatemic Rickets, Autosomal Recessive, 1 | Restrictive Dermopathy | Diastrophic Dysplasia | Generalized Epilepsy With Febrile Seizures Plus | Muscular Dystrophy | Primary Pigmented Nodular Adrenocortical Disease | Benign Familial Pemphigus | Hereditary Neuropathy With Liability To Pressure Palsies | Glucagonoma | Cerebellofaciodental Syndrome | Myoclonic Atonic Epilepsy | Sponastrime Dysplasia | Inflammatory Myopathy | Angelman Syndrome | Diabetes Type 2 | Renpenning Syndrome | Tangier Disease | Platelet Disorders | Alpers Syndrome | Congenital Poikiloderma | Chondrodysplasia Punctata 2, X-linked Dominant | Liddle Syndrome | Spinocerebellar Ataxia Type 13 | Pneumoconiosis | Panniculitis | Heart Block | Adrenomyeloneuropathy | Nemaline Myopathy 10 | Optic Atrophy 2 | 3C Syndrome | Dengue Hemorrhagic Fever | Chordoid Glioma | Sezary Syndrome | Congenital Dysfibrinogenemia | Bruck Syndrome | Pseudoexfoliation Syndrome | Retinal Diseases | Hamartoma | 5-oxoprolinase Deficiency | Mountain Sickness | Zimmermann-Laband Syndrome | Frontotemporal Dementia | Congenital Tufting Enteropathy | Shwachman-Bodian-Diamond Syndrome | B-cell Chronic Lymphocytic Leukemia | Meier-Gorlin Syndrome | Waldenstrom Macroglobulinemia | Ischemia | Uveitis, Anterior | Charcot-Marie-Tooth Disease, Type 1A | Aldosterone Synthase Deficiency | Guttate Psoriasis | Glioblastoma Multiforme | T-cell Leukemia | Antithrombin III Deficiency | Multiple Myeloma | Hyperinsulinism-hyperammonemia Syndrome | Iron Deficiency Anemia | Mitochondrial DNA Depletion Syndrome, Hepatocerebral Form | Crigler-Najjar Syndrome | Leishmaniasis, Cutaneous | Hemorrhoids | Spinocerebellar Ataxia Type 20 | Hypotension, Orthostatic | Niemann-Pick Disease, Type C | Progressive Familial Intrahepatic Cholestasis Type 3 | Chronic Leukemia | Hypertension, Renal | Leukoplakia, Oral | Very Long-chain Acyl-CoA Dehydrogenase Deficiency | Ganglioglioma | Plasmacytoma | Tibial Muscular Dystrophy | Colitis | Common Variable Immunodeficiency | Primary Cutaneous Amyloidosis | Dystrophy, Cone-rod | Panuveitis | Urea Cycle Disorder | Giant Cell Glioblastoma | Nephronophthisis | Fibromyalgia | Granuloma Annulare | Wolfram Syndrome 2 | Myeloid Leukemia | Porphyria, Acute Intermittent | Diabetes Insipidus | Methylmalonic Acidemia | Carotid Artery Disease | Sialoadenitis | Long QT Syndrome Type 1 | Hereditary Multiple Exostoses | Spinocerebellar Ataxia Type 21 | Kohlschutter-Tonz Syndrome | Rheumatic Heart Disease | Hypopigmentation | Progressive External Ophthalmoplegia | Brenner Tumor | Multiple Sclerosis, Chronic Progressive | Glycogen Storage Disease Type 5 | Astrocytoma | Oligospermia | Congenital Heart Block | Spinocerebellar Ataxia Type 12 | Tricho-hepato-enteric Syndrome | Pigment Dispersion Syndrome | Hemoglobinopathies | Van Der Knaap Disease | Ganglioneuroma | Swine Influenza | Atherosclerosis | Alcoholism | Anencephaly | Metabolic Diseases | Inflammatory Joint Disease | Kearns-Sayre Syndrome | Familial Digital Arthropathy-brachydactyly | Adams-Oliver Syndrome | Spasticity | Nutrition Disorders | Thyroid Dyshormonogenesis | Pelvic Inflammatory Disease | Schnitzler Syndrome | Keratosis, Actinic | Facioscapulohumeral Muscular Dystrophy Type 1 | Phenylketonuria | Hypohidrotic Ectodermal Dysplasia | Chondroma | IgA Deficiency | Empyema | Spinocerebellar Ataxia | Erectile Dysfunction | Pregnancy, Ectopic | Cholangiocarcinoma | Turner's Syndrome | Tyrosine Hydroxylase Deficiency | Stargardt Disease | Esotropia | Trigonocephaly | Haim-Munk Syndrome | Usher Syndrome Type I | Alpha-thalassemia Myelodysplasia Syndrome | Carcinoma In Situ | Sick Sinus Syndrome | Sporadic Inclusion Body Myositis | Transient Bullous Dermolysis Of The Newborn | Spinocerebellar Ataxia Type 14 | Sickle Cell Disease | Gangliosidosis | Hydrolethalus Syndrome | Inflammatory Linear Verrucous Epidermal Nevus | Retinal Vasculitis | Colitis, Microscopic | Gingivitis | Aplastic Anemia | Corticobasal Syndrome | Varicocele | Clouston Hidrotic Ectodermal Dysplasia | Myoclonus | Trismus-pseudocamptodactyly Syndrome | Vitamin K Deficiency | LMNA-related Congenital Muscular Dystrophy | Primary Aldosteronism | CDKL5 Deficiency Disorder | Hypertension, Pulmonary | Pneumonia, Mycoplasma | Desmosterolosis | Subacute Sclerosing Panencephalitis | Lesch-Nyhan Syndrome | Stroke | Histoplasmosis | Myelofibrosis | Renal Failure | Gastroenteritis, Eosinophilic | DOCK8 Immunodeficiency Syndrome | Triple A Syndrome | Spondylosis | Pneumonia, Viral | Nephrotic Syndrome | Dementia, Vascular | Dermatitis | Mast Cell Leukemia | Tic Disorder | WAGR Syndrome | Keratoconus | Pulmonary Veno-occlusive Disease | Histiocytic Sarcoma | Spinocerebellar Ataxia Type 40 | Pemphigus Foliaceus | Neuroblastoma | Vici Syndrome | Klippel-Feil Syndrome | Cohen Syndrome | Pulmonary Sclerosing Hemangioma | Bronchitis | Chylomicron Retention Disease | Myelodysplasia | Hepatitis E | Azoospermia | Twin-to-twin Transfusion Syndrome | Osteoporosis, Postmenopausal | X-linked Myotubular Myopathy | Asperger Syndrome | Fibrosarcoma | Purpura | Diabetes Mellitus, Transient Neonatal | Peroxisomal Disorder | Blue Nevus | Nephroblastoma | Compartment Syndrome | Scabies | Lamellar Ichthyosis | Lipid Metabolism Disorders | Pemphigus Vulgaris | Veno-occlusive Disease | Hereditary Sensory And Autonomic Neuropathy | Carpal Tunnel Syndrome | Apraxia | Sarcomatoid Carcinoma Of The Lung | Benign Hereditary Chorea | Brachydactyly | Low Phospholipid Associated Cholelithiasis | Intestinal Hypomagnesemia 1 | Presbyopia | Mumps | Chitayat Syndrome | Intellectual Disability, Autosomal Dominant 5 | Premature Ejaculation | AIDS Dementia Complex | Vitamin D Deficiency | Situs Inversus | Campomelic Dysplasia | Genee-Wiedemann Syndrome | Neuroma | Coffin-Siris Syndrome | Prader-Willi Syndrome | Poirier-Bienvenu Neurodevelopmental Syndrome | Cold-induced Sweating Syndrome | Paroxysmal Nocturnal Hemoglobinuria | Open-angle Glaucoma | Long QT Syndrome Type 2 | Parkinson Disease 6, Autosomal Recessive Early-onset | Budd-Chiari Syndrome | Meesmann Corneal Dystrophy | Corneal Edema | Pulmonary Alveolar Proteinosis | Migraine | Hermansky-Pudlak Syndrome | Vascular Calcification | Craniolenticulosutural Dysplasia | Chromosome 17q21.31 Deletion Syndrome | Chondrodysplasia Punctata 1, X-linked Recessive | Waardenburg Syndrome Type 1 | Epilepsy | Neuromyelitis Optica | Zygomycosis | Angina Pectoris | Neurotoxicity | Acrodermatitis Enteropathica | Trichotillomania | Papulopustular Rosacea | Onchocerciasis | Reticular Dysgenesis | Nephrosclerosis | Lattice Corneal Dystrophy | Cold Agglutinin Disease | Castleman Disease | Toxoplasmosis | Dyskeratosis Congenita | Osteonecrosis