Disease

Heart Septal Defects

About the Disease
Heart Septal Defect, also known as heart septal defects, is related to atrial septal defect 2 and atrial septal defect 5. An important gene associated with Heart Septal Defect is NKX2-5 (NK2 Homeobox 5), and among its related pathways/superpathways are Human Embryonic Stem Cell Pluripotency and 22q11.2 copy number variation syndrome. The drugs Acetylsalicylic acid and Clopidogrel have been mentioned in the context of this disorder. Affiliated tissues include heart, lung and endothelial, and related phenotypes are normal and muscle

Common Targets
ATIC | GART | MTHFD1 | FIGN | SHMT1

疾病靶点研报
Heart Septal Defects

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

Other Diseases

Hemangioma | Renpenning Syndrome | Kindler Syndrome | Parvovirus B19 Infection | Blepharo-cheilo-odontic Syndrome | Zimmermann-Laband Syndrome | Glycogen Storage Disease | Sleep Disorder | Esophageal Motility Disorders | Melanoma, Uveal | Chitayat Syndrome | X-linked Sideroblastic Anemia | Tumoral Calcinosis | Conjunctivitis | Chondrodysplasia Punctata 2, X-linked Dominant | Seizures | Xeroderma Pigmentosum Variant Type | Paraganglioma, Carotid Body | Chronic Granulomatous Disease | Cone Dystrophy | Goldenhar Syndrome | Lassa Fever | 3-methylglutaconic Aciduria Type IV | Restrictive Dermopathy | Shock, Cardiogenic | Hemophagocytic Lymphohistiocytosis | Ligneous Conjunctivitis | Ectodermal Dysplasia | Budd-Chiari Syndrome | LEOPARD Syndrome | Megalencephaly | Leishmaniasis, Visceral | Gastroschisis | Cholesteryl Ester Storage Disease | Skin Fragility-woolly Hair Syndrome | Woodhouse-Sakati Syndrome | 3C Syndrome | Primary Carnitine Deficiency | Spinocerebellar Ataxia Type 12 | Hemorrhagic Disorders | Brooke-Spiegler Syndrome | Distal Myopathy | Tetraplegia | Glycogen Storage Disease Type 1a | Wiskott-Aldrich Syndrome | Fukuyama Congenital Muscular Dystrophy | Systemic Lupus Erythematosus | Cutaneous Lupus Erythematosus | Teratozoospermia | Multisystemic Smooth Muscle Dysfunction Syndrome | Metachondromatosis | Hyperinsulinemic Hypoglycemia | Mycosis Fungoides | Imerslund-Grasbeck Syndrome | Iron Overload | Urticaria | Diabetic Nephropathy | Priapism | Thrombasthenia | Desmosterolosis | Megaloblastic Anemia | Neutropenia | Histoplasmosis | Amenorrhea | Charcot-Marie-Tooth Disease Type 2D | Chromosome 5q Deletion Syndrome | Lipid Metabolism Disorders | Neurofibroma, Plexiform | Facioscapulohumeral Muscular Dystrophy | Restless Legs Syndrome | Spondylocostal Dysostosis | GATA2 Deficiency | Vascular Cognitive Impairment | Craniopharyngioma | Distal Spinal Muscular Atrophy | Nephrosclerosis | Generalized Epilepsy With Febrile Seizures Plus | Oligoastrocytoma | Fuchs Heterochromic Iridocyclitis | Cholera | Charcot-Marie-Tooth Disease Type 2T | Dystonia Musculorum Deformans | Williams Syndrome | Schwannomatosis | Peroxisomal Disorder | Orthostatic Intolerance | Vertigo | Carcinoma, Merkel Cell | Primary Hyperoxaluria Type 1 | Carney Triad | Microcephaly | Spinocerebellar Ataxia Type 10 | Reticular Dysgenesis | Meckel-Gruber Syndrome | Familial Hyperaldosteronism | Pregnancy, Ectopic | Cholangitis | Lactose Intolerance | Growth Hormone Excess | Nicotine Addiction | Hoyeraal-Hreidarsson Syndrome | Polyradiculopathy | Tyrosinemia | Mohr-Tranebjaerg Syndrome | Poikiloderma With Neutropenia | Senior-Loken Syndrome | Schnitzler Syndrome | Sarcoma | Congenital Ichthyosiform Erythroderma | Trichotillomania | Sotos Syndrome | Acute Chest Syndrome | Gastritis, Atrophic | Cushing Syndrome | Mumps | Pseudohypoparathyroidism Type 1A | Meesmann Corneal Dystrophy | Sezary Syndrome | Hypercalciuria | Lattice Corneal Dystrophy | Follicular Dendritic Cell Sarcoma | Keratitis | Hypocalcemia | Wilson's Disease | Centronuclear Myopathy | Waardenburg Syndrome Type 4A | Joubert Syndrome | Creatine Deficiency Syndrome | Autoimmune Polyendocrine Syndrome | 3-methylglutaconic Aciduria Type I | Persistent Mullerian Duct Syndrome | Waardenburg Syndrome Type 2A | Ischemia | Osteoporosis-pseudoglioma Syndrome | Primary Lateral Sclerosis | Hepatic Veno-occlusive Disease | Autism | Renal Oncocytoma | Spinocerebellar Ataxia Type 16 | Hypertension | Allergic Contact Dermatitis | Porphyria, Acute Intermittent | Fuchs Dystrophy | Crouzon Syndrome With Acanthosis Nigricans | Oligodendroglioma | Atopy | Open-angle Glaucoma | Cancer, Skin | Analgesia | Hemoglobinopathies | Sarcomatoid Carcinoma Of The Lung | Familial Male-limited Precocious Puberty | Malaria | Neurofibroma | Medium-chain Acyl-CoA Dehydrogenase Deficiency | Meningioma | Primrose Syndrome | Graft-versus-host Disease | Narcolepsy | Gerstmann-Straussler-Scheinker Syndrome | Thrombocytopenia | Epidermolysis Bullosa Acquisita | Glomerulonephritis, Membranous | Gestational Trophoblastic Disease | Lymphopenia | Blomstrand Osteochondrodysplasia | Sclerosteosis 2 | Cranial Nerve Disease | Phenylketonuria | Kaposiform Hemangioendothelioma | Lymphomatoid Granulomatosis | Richter's Syndrome | Wagner Disease | Necrobiosis Lipoidica | Rickets | Cleidocranial Dysplasia | Tangier Disease | Salla Disease | D-2-Hydroxyglutaric Aciduria | Congenital Heart Defects | Hepatopulmonary Syndrome | Mitochondrial Myopathy | Hidradenitis | Spondyloepimetaphyseal Dysplasia With Joint Laxity, Type 3 | Fraser Syndrome | Non-Langerhans Cell Histiocytosis | Weill-Marchesani Syndrome | Low Phospholipid Associated Cholelithiasis | Pancreatitis | Hyperparathyroidism-jaw Tumor Syndrome | Mast Cell Leukemia | Leiomyoma | Hemorrhoids | Galloway-Mowat Syndrome | Desbuquois Syndrome | Panniculitis | Tetanus | Tracheal Disorders | Leukoplakia, Oral | Prurigo Nodularis | Cryptosporidiosis | Idiopathic Multicentric Castleman Disease | Gliosarcoma | Hemorrhage | Central Core Disease | Lichen Planus | Globozoospermia | Hypothalamic Obesity | Trichuriasis | Maternally Inherited Diabetes And Deafness | Hypertension, Pulmonary | Carbamoyl Phosphate Synthetase I Deficiency | Osteoarthritis | Nephrocalcinosis | Congenital Heart Block | Brugada Syndrome 1 | GNE Myopathy | Robinow Syndrome | Myeloid Leukemia | Nephrotic Syndrome Type 1 | Premenstrual Syndrome | Nanophthalmos | Sporadic Inclusion Body Myositis | Camptocormia | Hidradenitis Suppurativa | Beckwith-Wiedemann Syndrome | Kidney Stones | Non-epidermolytic Palmoplantar Keratoderma | Demyelinating Diseases | Lymphoma Lymphoblastic | Dystrophy, Cone-rod | Meconium Ileus | Binge Eating Disorder | Primary Torsion Dystonia | Hypolipoproteinemia | Parkinson Disease 6, Autosomal Recessive Early-onset | Heterotaxy | Seizures-scoliosis-macrocephaly Syndrome | Choroiditis | Neuroleptic Malignant Syndrome | Eating Disorder | Hydrocephalus, Normal Pressure | Cryoglobulinemia | Ehlers-Danlos Syndrome With Progressive Kyphoscoliosis, Myopathy, And Hearing Loss | Melanoma, Malignant | Netherton Syndrome | Retinopathy, Diabetic | Polymicrogyria | Osteochondrosis | Anodontia | Anorectal Malformations | Nephrotic Syndrome | Smith-Lemli-Opitz Syndrome | Corneal Neovascularization | Congenital Hereditary Endothelial Dystrophy Type II | Acne Vulgaris | Glucagonoma | Cri-du-chat Syndrome | Whipple's Disease | Hepatitis D | Myelodysplasia | Epidermolysis Bullosa Simplex With Mottled Pigmentation | Agranulocytosis | Shprintzen-Goldberg Syndrome | Exotropia | Withdrawal Syndrome | Antisynthetase Syndrome | Sleep Apnea, Obstructive | Dowling-Degos Disease | Hereditary Neuropathy With Liability To Pressure Palsies | Cold Agglutinin Disease | Pulverulent Zonular Cataract | Infantile Spasm | Pontocerebellar Hypoplasia | Proteasome-associated Autoinflammatory Syndrome 2 | Preaxial Polydactyly | Polycystic Ovary Syndrome | Chronic Neutrophilic Leukemia | Craniolenticulosutural Dysplasia | Adams-Oliver Syndrome | Cancer, Lung | Epidermolysis Bullosa Simplex, Localized | Prader-Willi Syndrome | Osteitis | Fahr Disease | Congenital Torticollis | Alexander Disease | Hypertension, Essential | Diamond-Blackfan Anemia | Camurati-Engelmann Disease | Spinal Muscular Atrophy | Gerodermia Osteodysplastica | Diarrhea | Leukocyte Adhesion Deficiency | Cardiofaciocutaneous Syndrome | Hypoalbuminemia | Thalassemia | Intestinal Obstruction | Cluster Headache | Ocular Surface Squamous Neoplasia | Glutaric Aciduria Type 3 | Medulloblastoma | Chronic Granulomatous Disease, X-linked | Pierre Robin Syndrome | Cerebellar Ataxia, Cayman Type | Intestinal Hypomagnesemia 1 | Glomerulonephritis, Membranoproliferative | ACTH-independent Macronodular Adrenal Hyperplasia | Anti-NMDA Receptor Encephalitis | Generalized Epilepsy And Paroxysmal Dyskinesia | Tendinitis | Gangliosidosis | Fabry's Disease | Methylmalonic Aciduria And Homocystinuria, CblC Type | Rheumatoid Arthritis | Dyskeratosis Congenita | Cholestasis, Intrahepatic | Waldenstrom Macroglobulinemia | Duane Retraction Syndrome | Spinocerebellar Ataxia Type 8 | Thyroiditis | Basal Ganglia Cerebrovascular Disease | Occipital Neuralgia | Peyronie's Disease | Niemann-Pick Disease, Type B | Atopic Dermatitis | Wolman Disease | Cirrhosis | Pitt-Hopkins Syndrome | Pyelonephritis | Thin Basement Membrane Disease | Antisocial Personality Disorder | Ulcerative Colitis | CREST Syndrome | Myhre Syndrome | Benign Familial Infantile Seizures | Opisthorchiasis | Hartnup Disease | Spondyloarthritis | Hypertension, Renovascular | Long QT Syndrome Type 1 | Allan-Herndon-Dudley Syndrome | Multiple Hamartoma Syndrome | Familial Hemiplegic Migraine | Pupil Disorders | Congenital Fiber-type Disproportion Myopathy | Vaginitis | Nicotine Dependence | Congenital Myasthenic Syndrome | Cervicitis | Huntington's Disease-like 2 | Cartilage Disorders | Giant Cell Glioblastoma | Sengers Syndrome | IMAGe Syndrome | Stroke, Ischemic | IgA Nephropathy | Hereditary Spherocytosis | Jalili Syndrome | Leukodystrophies | Meniere's Disease | Fontaine Progeroid Syndrome | Hypertelorism | Chordoma | Botulism | Alpha-thalassemia Myelodysplasia Syndrome | Angiosarcoma | Hyperparathyroidism, Secondary | Endocarditis | Intestinal Tuberculosis | Lissencephaly 2 | Hyperkeratosis | NGLY1 Deficiency | Hyperuricemic Nephropathy, Familial Juvenile | Cerebrovascular Disorders | Enterocolitis, Necrotizing | Androgenic Alopecia | Carcinoma, Signet Ring Cell | Mucormycosis | Insulin Resistance | Presbycusis | Blue Nevus | Nephritis, Interstitial | Cousin Syndrome | Spinocerebellar Ataxia | Paraganglioma | Thyroiditis, Autoimmune | Encephalopathy, Ethylmalonic | Carotid Artery Disease | Muscular Dystrophy | Charcot-Marie-Tooth Disease, Type 2C | Epithelial-myoepithelial Carcinoma | Neuropathy | Melnick-Needles Syndrome | Stomatitis | Optic Nerve Hypoplasia, Bilateral | Werner's Syndrome | Presbyopia | Oguchi Disease-2 | Asperger Syndrome