Disease

Holt-Oram Syndrome

About the Disease
Holt-Oram Syndrome, also known as hos, is related to interatrial communication and aortic valve disease 2. An important gene associated with Holt-Oram Syndrome is TBX5 (T-Box Transcription Factor 5), and among its related pathways/superpathways are Cardiac conduction and Human Embryonic Stem Cell Pluripotency. Affiliated tissues include heart, upper limb and bone, and related phenotypes are joint stiffness and split hand

Common Targets
RYR2 | TBX5 | LMNA | Transcriptional Enhancer Factor (TEAD) (nonspecified subype) | G10413

疾病靶点研报
Holt-Oram Syndrome

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

Other Diseases

Acute Leukemia | Rheumatic Heart Disease | Combined Pituitary Hormone Deficiency | Leukemia-lymphoma, Adult T-cell | Spinocerebellar Ataxia Type 15 | Progressive Familial Intrahepatic Cholestasis Type 1 | Congenital Adrenal Hyperplasia | Shprintzen-Goldberg Syndrome | Ataxia-ocular Apraxia 2 | Colitis | Ollier Disease | Adenoma, Pleomorphic | Familial Exudative Vitreoretinopathy | Pulmonary Alveolar Microlithiasis | Alexander Disease | Diffuse Mesangial Sclerosis | Charcot-Marie-Tooth Disease Type 2E | SAPHO Syndrome | Hereditary Hemorrhagic Telangiectasia Type 2 | Hemangioblastoma | Bone Marrow Necrosis | Gastric Atrophy | Hyperekplexia | Hypertensive Retinopathy | Spinocerebellar Ataxia Type 13 | Hyperglycemia | Polymicrogyria | Spinocerebellar Ataxia Type 20 | Split Hand-foot Malformation | Ganglioneuroma | Low Phospholipid Associated Cholelithiasis | Niemann-Pick Disease | Waardenburg Syndrome Type 2 | Spinocerebellar Ataxia Type 14 | Bronchiectasis | Diamond-Blackfan Anemia | Osteogenesis Imperfecta Type V | Seizures-scoliosis-macrocephaly Syndrome | Cerebellofaciodental Syndrome | Porphyria | Nephropathy | Frank-ter Haar Syndrome | Spinocerebellar Ataxia Type 2 | Spinocerebellar Ataxia Type 7 | Huntington's Disease-like 2 | Primary Biliary Cholangitis | Cerebral Cavernous Malformations | Hypophosphatasia | Xeroderma Pigmentosum | Phosphoglycerate Dehydrogenase Deficiency | Galactosialidosis | Rhabdomyosarcoma, Embryonal | Tremor | Sclerocornea | Pigment Dispersion Syndrome | Alpers Syndrome | Bare Lymphocyte Syndrome | Epidermolysis Bullosa | Subacute Sclerosing Panencephalitis | Dwarfism | Juvenile Myoclonic Epilepsy | Colitis, Collagenous | Klippel-Feil Syndrome | Coloboma | Fibrosarcoma | DiGeorge Syndrome | Central Pain Syndrome | Diffuse Intrinsic Pontine Glioma | T-cell Leukemia | Wiskott-Aldrich Syndrome | Blomstrand Osteochondrodysplasia | Prolymphocytic Leukemia | Optic Neuropathy, Anterior Ischemic | ADNP Syndrome | Congenital Muscular Dystrophy | Cholelithiasis | Heart Block | Poikiloderma With Neutropenia | Acrodermatitis | Osteitis | Hepatic Veno-occlusive Disease | Ehlers-Danlos Syndrome | Sclerosing Cholangitis | Pulmonary Vein Stenosis | Mumps | Fibromuscular Dysplasia | Niemann-Pick Disease, Type C | Farber Disease | Idiopathic Pulmonary Fibrosis | Trichothiodystrophy | Hidradenitis | Central Core Disease | Ventricular Septal Defect | Epidermolytic Palmoplantar Keratoderma | Citrullinemia | Infantile Liver Failure Syndrome 1 | Craniofacial Dysostosis | Hyperinsulinemia | Cancer, Lung | Fahr Disease | Snyder-Robinson Syndrome | Diabetes Type 1 | Acute Lung Injury | Left Ventricular Noncompaction | Creatine Deficiency Syndrome Due To AGAT Deficiency | Cardiac Sarcoidosis | Imerslund-Grasbeck Syndrome | Congenital Bile Acid Synthesis Defect | Microphthalmia, Syndromic 7 | Polycystic Ovary Syndrome | Acne Vulgaris | Atopic Dermatitis | Renal Medullary Carcinoma | Angelman Syndrome | Mesothelioma, Malignant | Pachyonychia Congenita | Noonan Syndrome-like Disorder With Loose Anagen Hair | Gerstmann-Straussler-Scheinker Syndrome | Reticular Dysgenesis | Blue Nevus | Tuberculous Meningitis | Urofacial Syndrome | Follicular Dendritic Cell Sarcoma | Congenital Myopathy | Nail Disorder, Nonsyndromic Congenital | Pseudomyxoma Peritonei | Scleritis | Spinocerebellar Ataxia Type 3 | Corneal Dystrophy | Disseminated Intravascular Coagulation | Arthritis, Psoriatic | Neutrophilia | Neuroma | Stevens-Johnson Syndrome | Cysticercosis | Acute Lymphocytic Leukemia | Glomerulonephritis, Membranoproliferative | Menkes Disease | Intellectual Disability, Autosomal Dominant 5 | Blepharospasm | Lipid Metabolism Disorders | Myhre Syndrome | Pseudoachondroplasia | Infantile Nephropathic Cystinosis | Esophageal Motility Disorders | Ischemia | Acromicric Dysplasia | Auriculocondylar Syndrome | Impetigo | Alkaptonuria | Gangliosidosis, GM1 | Corneal Dystrophies, Hereditary | Congenital Heart Block | Kallmann Syndrome | Congenital Lipoid Adrenal Hyperplasia | Ebstein Anomaly | Neurocysticercosis | Thrombasthenia | Thrombotic Microangiopathy | Familial Pheochromocytoma-paraganglioma | X-linked Charcot-Marie-Tooth Disease | Malaria | Congenital Dysfibrinogenemia | Temporal Lobe Epilepsy | Hyperbilirubinemia, Neonatal | Macrophage Activation Syndrome | Erythema Nodosum | Sleep Disorder | Lupus Erythematosus | Echinococcosis | Acute Chest Syndrome | Barrett Esophagus | Rett Syndrome | Alstrom Syndrome | Angiosarcoma Of The Breast | HIBCH Deficiency | Pemphigus Foliaceus | Congenital Nystagmus | Thyroid Dysgenesis | Deafness, Dystonia, And Cerebral Hypomyelination | Vascular Cognitive Impairment | Pendred Syndrome | Renpenning Syndrome | Pyruvate Dehydrogenase Deficiency | Hepatitis C, Chronic | Lymphoma, Primary Cutaneous Anaplastic Large Cell | Dyslexia | Paget's Disease Of The Breast | Loeys-Dietz Syndrome Type 4 | Mycosis Fungoides | Focal Segmental Glomerulosclerosis | Spinocerebellar Ataxia Type 27 | Hepatorenal Syndrome | Brachial Plexus Neuropathy | Primary Torsion Dystonia | IgA Deficiency | Nephrocalcinosis | Schistosomiasis Mansoni | Leukodystrophies | Arthrogryposis | Ellis-Van Creveld Syndrome | Thin Basement Membrane Disease | Hypohidrotic Ectodermal Dysplasia | Conn Syndrome | Sleep Apnea, Central | Schizencephaly | Krabbe Disease | Adenylosuccinate Lyase Deficiency | B-cell Chronic Lymphocytic Leukemia | ICF Syndrome | Pulverulent Zonular Cataract | Hemorrhage | Ichthyosis Hystrix, Curth-Macklin Type | Fuchs Dystrophy | Myositis, Focal | Renal Hypomagnesemia 3 | Spondylo-ocular Syndrome | Mabry Syndrome | Dent Disease | Exotropia | Hyperphosphatasia With Intellectual Disability Syndrome 4 | Azoospermia | Stargardt Disease | Incontinentia Pigmenti | Uveitis | Hemoglobinopathies | Impulse Control Disorder | Familial Digital Arthropathy-brachydactyly | Hepatitis A | Psoriasis | Spinal Muscular Atrophy With Progressive Myoclonic Epilepsy | Bacterial Meningitis | Acquired Partial Lipodystrophy | Fibromyalgia | Glutaric Aciduria Type 1 | Acute Anterior Uveitis | Aphasia | Polycystic Kidney, Autosomal Recessive | Erythrokeratodermia Variabilis | Trismus-pseudocamptodactyly Syndrome | Schizophrenia, Paranoid | Keratitis | Mood Disorder | Hepatitis | Silicosis | Pycnodysostosis | Erythema Multiforme | Borderline Personality Disorder | Zollinger-Ellison Syndrome | Asplenia | Cellulitis | Stomatitis | Meesmann Corneal Dystrophy | Seizures | Presbycusis | Phosphoenolpyruvate Carboxykinase Deficiency, Cytosolic | Hypertrophy | Spinal Cord Diseases | Craniometaphyseal Dysplasia | Chronic Lymphocytic Leukemia | Pneumothorax | Thanatophoric Dysplasia Type 1 | Heavy Chain Disease | Dementia, Vascular | Primary Hyperoxaluria Type 1 | Oculocutaneous Albinism Type 1 | Rhabdomyosarcoma, Alveolar | Leiomyoma | Postpoliomyelitis Syndrome | Optic Nerve Diseases | Inflammatory Linear Verrucous Epidermal Nevus | Amyotrophic Lateral Sclerosis | Transient Bullous Dermolysis Of The Newborn | Rift Valley Fever | Progressive External Ophthalmoplegia | Guttate Psoriasis | Lentigo | Oligoastrocytoma | Neuromyelitis Optica | Premenstrual Syndrome | Erythromelalgia | Hemochromatosis Type 2 | Alpha-mannosidosis | Duchenne Muscular Dystrophy | Thymoma, Malignant | Actinomycetoma | Granuloma Annulare | Facioscapulohumeral Muscular Dystrophy Type 2 | Walker-Warburg Syndrome | Familial Episodic Pain Syndrome | Chromosome 16p11.2 Deletion Syndrome | Stiff-man Syndrome | MIRAGE Syndrome | 3-hydroxy-3-methylglutaric Aciduria | Tardive Dyskinesia | Congenital Heart Defects | Alazami Syndrome | Mucolipidosis Type IV | Uremia | Batten Disease | Bronchiolitis | Ameloblastic Carcinoma | Spinal Muscular Atrophy Type 3 | Primary Progressive Aphasia | Choroideremia | Cerebrotendinous Xanthomatosis | Sclerosteosis 2 | Partington Syndrome | Infertility | Charcot-Marie-Tooth Disease Type 4D | Hernia, Inguinal | Gnathodiaphyseal Dysplasia | Aneurysm, Abdominal Aortic | Cyst | Lymphangioleiomyomatosis | Multiple System Atrophy | Nance-Horan Syndrome | Strabismus | Blastoma, Pleuropulmonary | Ureteropelvic Junction Obstruction | Congenital Generalized Lipodystrophy | Alpha-1 Antitrypsin Deficiency | Meningeal Melanocytoma | Osteochondroma | Spondylo-megaepiphyseal-metaphyseal Dysplasia | Leprosy | Triple A Syndrome | Chronic Myelomonocytic Leukemia | Thalassemia, Beta | Leukoplakia, Oral | Aldosterone Deficiency | Intermittent Claudication | Keratopathy | Myoclonus | Macular Corneal Dystrophy | Neurofibrosarcoma | Hoyeraal-Hreidarsson Syndrome | Astrocytoma | Multiple Sclerosis, Primary Progressive | Sengers Syndrome | Medulloblastoma | Intracerebral Hemorrhage | Carcinoma, Squamous Cell | Jacobsen Syndrome | Tetraplegia | Skin Fragility-woolly Hair Syndrome | Kohlschutter-Tonz Syndrome | Dermatitis Herpetiformis | Periodic Limb Movement Disorder | Spasticity | Poirier-Bienvenu Neurodevelopmental Syndrome | 3-methylcrotonyl-CoA Carboxylase Deficiency | Gingivitis | Primary Progressive Nonfluent Aphasia | T-cell Lymphoma, Subcutaneous Panniculitis-like | Lymphoma, AIDS-related | Lyme Disease | Frontotemporal Dementia With Amyotrophic Lateral Sclerosis | Adenosine Deaminase Deficiency | Familial Thoracic Aortic Aneurysm | Schaaf-Yang Syndrome | Paracoccidioidomycosis | Microcephaly, Seizures, And Developmental Delay | Infantile Refsum Disease | Cohen Syndrome | Veno-occlusive Disease | Exostoses | Episodic Ataxia Type 1 | Brugada Syndrome 1 | CHARGE Syndrome | Scapuloperoneal Myopathy, X-linked Dominant | Osteomyelitis | Mitochondrial Myopathy | Multisystemic Smooth Muscle Dysfunction Syndrome | Stroke | Asthma, Exercise-induced | Niemann-Pick Disease, Type A | Rhizomelic Chondrodysplasia Punctata | Cutaneous T-cell Lymphoma | Presbyopia | Greig Cephalopolysyndactyly Syndrome | Jaundice, Obstructive | IgA Nephropathy | Trichorhinophalangeal Syndrome | Polycystic Kidney, Autosomal Dominant | PASLI Disease | Proximal Symphalangism | Congestive Heart Failure | Cervicitis | Intestinal Pseudo-obstruction | Glomerulonephritis | Smoldering Myeloma | Measles | Encephalitis | Familial Advanced Sleep Phase Syndrome | Wieacker-Wolff Syndrome | Richter's Syndrome | Primary Familial Brain Calcification | Mandibuloacral Dysplasia With Type A Lipodystrophy | Ectodermal Dysplasia