Disease

Hypoplastic Left Heart Syndrome

About the Disease
Hypoplastic Left Heart Syndrome, also known as hlhs, is related to aortic valve disease 2 and aortic valve disease 1. An important gene associated with Hypoplastic Left Heart Syndrome is TBX20 (T-Box Transcription Factor 20), and among its related pathways/superpathways are Embryonic and Induced Pluripotent Stem Cells and Lineage-specific Markers and Neural crest differentiation. The drugs Ambrisentan and Sildenafil have been mentioned in the context of this disorder. Affiliated tissues include heart, skin and brain, and related phenotypes are hypoplastic left heart and hypoplastic aortic arch

Common Targets
G4851 | ADRA2A | FOXP1 | NKX2-5 | RAF1 | ADRB1 | HMCN1 | TBX5 | PTPRB | NR2F2 | MYH6 | FOXL1 | FOXC2 | HEYL | HEY2 | MYH7 | MYRF

疾病靶点研报
Hypoplastic Left Heart Syndrome

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

Other Diseases

Crisponi Syndrome | Double Outlet Right Ventricle | Vitiligo | Delirium | Nephroblastoma | Pituitary Dwarfism | Pemphigus Foliaceus | Hepatitis D | Tetraplegia | Pyelonephritis | Congenital Bilateral Absence Of Vas Deferens | Chronic Lymphocytic Leukemia | Combined Pituitary Hormone Deficiency | Common Cold | Cutis Laxa | NDH Syndrome | Coloboma | Neuroleptic Malignant Syndrome | Language Disorders | Stuttering | Early Infantile Epileptic Encephalopathy 1 | Mannosidase Deficiency Diseases | Adenomyosis | Spinocerebellar Ataxia Type 2 | Takenouchi-Kosaki Syndrome | PHARC Syndrome | Nicotine Dependence | Fanconi Anemia | Macrophagic Myofasciitis | Globozoospermia | Adenomatoid Tumor | Hypothyroidism | Thyroiditis, Autoimmune | Congenital Poikiloderma | Gerodermia Osteodysplastica | Cholangitis | Hepatic Steatosis | Intracranial Hypertension | Ulcerative Colitis | Osteonecrosis | Pleurisy | Retinal Dystrophy | Chromosome 17q21.31 Deletion Syndrome | Crimean-Congo Hemorrhagic Fever | Delayed Sleep Phase Syndrome | Lymphangiomatosis | Coronary Heart Disease | Primary Erythromelalgia | Optic Neuropathy, Anterior Ischemic | 17-beta-hydroxysteroid Dehydrogenase X Deficiency | Sarcomatoid Carcinoma Of The Lung | Infantile Liver Failure Syndrome 1 | Hyperbilirubinemia, Neonatal | Encephalitis | Hypohidrotic Ectodermal Dysplasia | Rosacea | SAPHO Syndrome | Congenital Myopathy | Corneal Dystrophy And Perceptive Deafness | Lathosterolosis | Charcot-Marie-Tooth Disease Type 2D | Venous Insufficiency | Glycogen Storage Disease Type 0, Muscle | Progressive External Ophthalmoplegia | Encephalopathy | DEND Syndrome | Temtamy Preaxial Brachydactyly Syndrome | Spondylocostal Dysostosis | Anorectal Malformations | Ganglioneuroma | Fuchs Dystrophy | Eosinophilic Asthma | Crouzon Syndrome With Acanthosis Nigricans | Episodic Ataxia Type 1 | Glucagonoma | Schwartz-Jampel-Aberfeld Syndrome | Neurodevelopmental Disorders | Joubert Syndrome 2 | Macrodactyly | Waardenburg Syndrome Type 2E | Systemic Lupus Erythematosus | Plasma Cell Leukemia | Borjeson-Forssman-Lehmann Syndrome | T-cell Chronic Lymphocytic Leukemia | Zellweger Syndrome | Liver Diseases | Chondroma | Pancreatitis | Pulmonary Veno-occlusive Disease | Spinocerebellar Ataxia Type 16 | Epilepsy | Neurogenic Bladder | Christianson Syndrome | Macular Corneal Dystrophy | Bone Giant Cell Tumor | Early Infantile Epileptic Encephalopathy 13 | Salla Disease | Waardenburg Syndrome | Cholelithiasis | Hyperparathyroidism, Secondary | Benign Familial Infantile Seizures | Follicular Dendritic Cell Sarcoma | Conduct Disorder | Cataplexy | Kabuki Syndrome 2 | C3 Glomerulonephritis | ACTH-independent Macronodular Adrenal Hyperplasia | Knobloch Syndrome | Peeling Skin Syndrome Type B | Pneumonia, Mycoplasma | Sensorineural Hearing Loss | Glycogen Storage Disease Type 3 | Central Retinal Artery Occlusion | Arthritis, Psoriatic | Cystinuria | Blue Nevus | Chromosome 9q34.3 Deletion Syndrome | Analgesia | Leber Hereditary Optic Neuropathy | Lymphoma | Distal Spinal Muscular Atrophy | Hypertension, Portal | Charcot-Marie-Tooth Disease, Type 2A | Cold-induced Sweating Syndrome | Sickle Cell Disease | Hypoplastic Left Heart Syndrome | Glycogen Storage Disease | Aplasia Cutis Congenita | Infertility | Primary Progressive Nonfluent Aphasia | Hairy Cell Leukemia | Exocrine Pancreatic Insufficiency | Trismus-pseudocamptodactyly Syndrome | Neurodermatitis | Acral Lentiginous Melanoma | Charcot-Marie-Tooth Disease Type 4 | Ellis-Van Creveld Syndrome | Exfoliative Dermatitis | Osteonecrosis Of The Jaw | Cholestasis, Intrahepatic | Pompe Disease | Coronary Restenosis | Cardiac Arrest | Mandibuloacral Dysplasia With Type A Lipodystrophy | Hepatorenal Syndrome | Hemophagocytic Lymphohistiocytosis | VEXAS Syndrome | Diabetes Insipidus | Pontocerebellar Hypoplasia | Angioedema | Orthostatic Intolerance | Pierpont Syndrome | X-linked Creatine Transporter Deficiency | Peters-plus Syndrome | Gastritis | Dowling-Degos Disease | Prostatitis | McCune-Albright Syndrome | Neurocutaneous Syndromes | Congenital Mirror Movements | Cystitis | Parvovirus B19 Infection | Lupus Erythematosus | Congenital Sodium Diarrhea | Autoimmune Interstitial Lung, Joint, And Kidney Disease | Multicentric Carpotarsal Osteolysis Syndrome | Hyperinsulinism-hyperammonemia Syndrome | Epidermolysis Bullosa Simplex, Dowling-Meara Type | Peritonitis | Fatty Aldehyde Dehydrogenase Deficiency | Encephalopathy, Hepatic | Succinic Semialdehyde Dehydrogenase Deficiency | Hyperthermia, Malignant | Benign Hereditary Chorea | Lennox-Gastaut Syndrome | Pachyonychia Congenita | Galloway-Mowat Syndrome | Insulinoma | Achromatopsia | Cryopyrin-associated Periodic Syndromes | Nicolaides-Baraitser Syndrome | Peutz-Jeghers Syndrome | Obesity, Morbid | Corneal Dystrophy | Congenital Heart Defects | Pyruvate Kinase Deficiency | Neurofibromatosis Type 2 | Smith-Magenis Syndrome | Chondrosarcoma | Angiosarcoma | Hypercalcemia | Hypothalamic Obesity | Congenital Hemolytic Anemia | Dentinogenesis Imperfecta | Tylosis With Esophageal Cancer | Spina Bifida | Scleritis | Congenital Ichthyosiform Erythroderma | Chromosome 16p11.2 Deletion Syndrome | Kaposi Sarcoma | Usher Syndrome Type II | Dupuytren Disease | Arthritis, Gouty | Retinopathy Of Prematurity | Amenorrhea | Atelosteogenesis Type 1 | Trigonocephaly | Cutaneous Angiosarcoma | Saethre-Chotzen Syndrome | Pontocerebellar Hypoplasia Type 7 | Congenital Hereditary Endothelial Dystrophy Type II | Anencephaly | Charcot-Marie-Tooth Disease Type 3 | Melanoma, Uveal | Lymphoma, AIDS-related | Silver-Russell Syndrome | Wiskott-Aldrich Syndrome | Creatine Deficiency Syndrome Due To AGAT Deficiency | Lymphedema-distichiasis Syndrome | Spinocerebellar Ataxia Type 7 | Hydronephrosis | Eclampsia | Duane Retraction Syndrome | Chitayat Syndrome | Chronic Granulomatous Disease, X-linked | Focal Dermal Hypoplasia | Fibronectin Glomerulopathy | Trichuriasis | Iron Deficiency Anemia | Charcot-Marie-Tooth Disease Type 2E | Familial Retinal Arterial Macroaneurysm | Chronic Granulomatous Disease | Autonomic Nervous System Disorders | Chondrodysplasia Punctata 2, X-linked Dominant | Anorexia Nervosa | Anterior Segment Dysgenesis | Ectrodactyly | Roberts Syndrome | Fabry's Disease | Mitochondrial Encephalomyopathy | Werner's Syndrome | Neovascular Glaucoma | Phosphoenolpyruvate Carboxykinase Deficiency, Cytosolic | Metatropic Dysplasia | Gestational Trophoblastic Disease | Schwannoma | Myoclonus-dystonia Syndrome | Osteogenesis Imperfecta Type I | Microcephaly | Hyperparathyroidism | Proteasome-associated Autoinflammatory Syndrome 2 | X-linked Myotubular Myopathy | Creatine Deficiency Syndrome | GLUT1 Deficiency Syndrome | Primary Carnitine Deficiency | Meckel-Gruber Syndrome | Mitochondrial Myopathy | Yellow Fever | Pyruvate Dehydrogenase Deficiency | Blau Syndrome | Rubinstein-Taybi Syndrome | Epicondylitis | Branchiootorenal Syndrome | Paraplegia | Neurodegeneration Due To Cerebral Folate Transport Deficiency | Congenital Absence Of Vas Deferens | Micropenis | Desbuquois Syndrome | Keratopathy | Hyperferritinemia-cataract Syndrome | Granular Corneal Dystrophy Type 1 | Palmoplantar Keratoderma | Relapsing Polychondritis | Encephalocele | Blepharospasm | WAGR Syndrome | Restless Legs Syndrome | Heroin Dependence | Episodic Ataxia | Hemochromatosis Type 2 | Amyotrophic Lateral Sclerosis-parkinsonism-dementia Complex | Glaucoma, Congenital | Diabetes Type 2 | IMAGe Syndrome | Lymphoma, Follicular | Spinocerebellar Ataxia Type 28 | Nevus | GM2-gangliosidosis AB Variant | Posterior Polar Cataract | Pancytopenia | Partington Syndrome | Otosclerosis | C3 Glomerulopathy | Acute Motor Axonal Neuropathy | Maple Syrup Urine Disease | Poikiloderma With Neutropenia | Neutrophilia | Carbohydrate Metabolism Disorders | Leukocyte Adhesion Deficiency | Guttate Psoriasis | Chorea | Nephronophthisis | Dermatomyositis | Patent Ductus Arteriosus | Retinopathy, Diabetic | Oculocutaneous Albinism Type 2 | Cystinosis | Periventricular Nodular Heterotopia | X-linked Acrogigantism | Optic Nerve Hypoplasia, Bilateral | Interstitial Lung Diseases | Poirier-Bienvenu Neurodevelopmental Syndrome | Pathological Gambling | Asthma, Nocturnal | Spinocerebellar Ataxia | Prurigo Nodularis | Epithelioid Hemangioma | Intellectual Disability, Autosomal Dominant 5 | Ameloblastoma | Carney Triad | Bartsocas-Papas Syndrome | Basal Ganglia Disease | Campomelic Dysplasia | DOCK8 Immunodeficiency Syndrome | Adult Polyglucosan Body Disease | Osteosarcoma | Adams-Oliver Syndrome | Pneumothorax | Wolfram Syndrome | Basan Syndrome | Fibrosis | 3-hydroxyacyl-CoA Dehydrogenase Deficiency | Protein C Deficiency | Uveitis, Anterior | Osteitis | Metaphyseal Chondrodysplasia, Schmid Type | Hyperthyroidism | Uremia | Avellino Corneal Dystrophy | Chloridorrhea, Congenital | Spinocerebellar Ataxia Type 1 | Acute Kidney Injury | Trachoma | Aspartylglycosaminuria | Combined Malonic And Methylmalonic Acidemia | Pigment Dispersion Syndrome | Raynaud Phenomenon | Agammaglobulinemia | Chondrodysplasia Punctata | Angioedema, Hereditary | Irritable Bowel Syndrome | Ataxia-ocular Apraxia 2 | Adenosine Deaminase Deficiency | Portal Vein Thrombosis | ICF Syndrome | Erythrokeratodermia Variabilis | Tumoral Calcinosis | Arterial Tortuosity Syndrome | Olmsted Syndrome | Cardiomyopathy, Dilated, 1L | Proximal Symphalangism | Schistosomiasis | Myofibrillar Myopathy | Congenital Dyserythropoietic Anemia | Pulmonary Sclerosing Hemangioma | Muscle Wasting | Diabetic Neuropathy | Polycystic Kidney, Autosomal Dominant | Pemphigus | Burn-McKeown Syndrome | Sialoadenitis | Lymphopenia | Primary Aldosteronism | Epidermolytic Hyperkeratosis | Spinocerebellar Ataxia Type 3 | Dysthymia | Peeling Skin Syndrome, Acral Type | Hypokalemic Periodic Paralysis | Vertigo | Retinitis | Milk Allergy | Gingivitis | Choroideremia | Hypoproteinemia, Hypercatabolic | Multiple Sclerosis, Chronic Progressive | Acute Coronary Syndrome | Keratitis-ichthyosis-deafness Syndrome | Bicuspid Aortic Valve | Autosomal Recessive Spastic Paraplegia Type 35 | Cystitis, Interstitial | Myopia | Cerebellar Ataxia, Cayman Type | Tracheal Disorders | Sialidosis | Anodontia | Pseudohypoparathyroidism Type 1C | Keratosis | Schamberg Disease | Ectopia Lentis, Isolated, Autosomal Recessive | Histiocytosis