Disease

Dilated, 1L Cardiomyopathy

About the Disease
Cardiomyopathy, Dilated, 1l, also known as dilated cardiomyopathy 1l, is related to autosomal recessive limb-girdle muscular dystrophy type 2c and muscular dystrophy, limb-girdle, autosomal recessive 6. An important gene associated with Cardiomyopathy, Dilated, 1l is SGCD (Sarcoglycan Delta), and among its related pathways/superpathways are Extracellular matrix organization and Initial triggering of complement. Affiliated tissues include heart, skeletal muscle and heart-atrium, and related phenotypes are sudden cardiac death and congestive heart failure

Common Targets
AGT | AGTR1 | SLCO1B1

疾病靶点研报
Dilated, 1L Cardiomyopathy

Note: If you'd like to get a target analysis report for Dilated, 1L Cardiomyopathy, 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 Dilated, 1L Cardiomyopathy at a cost 90% lower than traditional approaches, please feel free to contact us at BD@silexon.ai.

Other Diseases

Saethre-Chotzen Syndrome | Ileitis | Keratitis-ichthyosis-deafness Syndrome | Adenoma, Pituitary | Tetraplegia | Conjunctivitis, Allergic | Spinal Cord Diseases | Unverricht-Lundborg Syndrome | Smith-Lemli-Opitz Syndrome | Dystonia | Cancer, Colon | Hypoparathyroidism | Raynaud Phenomenon | Peritonitis | Hepatitis | Angioedema, Acquired | Menetrier Disease | Spondylolisthesis | Multisystemic Smooth Muscle Dysfunction Syndrome | Transcobalamin Deficiency | Trichorhinophalangeal Syndrome | Tumoral Calcinosis | Potocki-Shaffer Syndrome | Leiomyosarcoma | Prurigo Nodularis | Familial Digital Arthropathy-brachydactyly | Autosomal Recessive Bestrophinopathy | Neurodegeneration Due To Cerebral Folate Transport Deficiency | Episodic Ataxia | Pyruvate Kinase Deficiency | Exotropia | Alpha-thalassemia Myelodysplasia Syndrome | Stuttering | Familial Retinal Arterial Macroaneurysm | GATA2 Deficiency | Trigonocephaly | Carcinoid Syndrome | Biotinidase Deficiency | Cherubism | Meningococcal Infections | Coronary Artery Disease | Skin Papilloma | Learning Disability | Costello Syndrome | Pitt-Hopkins Syndrome | Dysferlinopathy | Arts Syndrome | Cancer, Lung | Schamberg Disease | Synovitis | Parkinson's Disease | Von Hippel-Lindau Disease | HUPRA Syndrome | Lymphangioleiomyomatosis | Benign Familial Pemphigus | Usher Syndrome Type III | Aarskog-Scott Syndrome | Kaposiform Hemangioendothelioma | Rhabdomyosarcoma, Alveolar | Adenoma, Villous | Fahr Disease | Epidermolysis Bullosa Simplex, Dowling-Meara Type | Infantile Liver Failure Syndrome 1 | Angioimmunoblastic T-cell Lymphoma | Epidermolysis Bullosa Simplex, Generalized | Corneal Ulcer | Amyotrophic Lateral Sclerosis, Juvenile | Polyomavirus Nephropathy | Charcot-Marie-Tooth Disease Type 4D | Epiphyseal Chondrodysplasia, Miura Type | Asthma, Nocturnal | Citrullinemia | Loeys-Dietz Syndrome | Greig Cephalopolysyndactyly Syndrome | Cutis Laxa | Leiomyoma | Hypersensitivity Pneumonitis | Hypospadias | DICER1 Syndrome | Hypohidrotic Ectodermal Dysplasia | Basal Ganglia Disease, Biotin-responsive | Borjeson-Forssman-Lehmann Syndrome | Chromosome 8q21.11 Deletion Syndrome | Haim-Munk Syndrome | Chronic Myeloid Leukemia | Beckwith-Wiedemann Syndrome | Centronuclear Myopathy | Sick Sinus Syndrome 1 | Dementia | Aceruloplasminemia | Infantile Nephropathic Cystinosis | Juvenile Hyaline Fibromatosis | Ventricular Septal Defect | Placenta Previa | Cone Dystrophy | Adrenal Insufficiency | Papilloma | Cousin Syndrome | Osteoarthritis | Neutrophilia | Charcot-Marie-Tooth Disease, Type 6 | Chondrodysplasia Punctata | Sweet Syndrome | Thanatophoric Dysplasia | Cancer, Kidney | Impulse Control Disorder | Congenital Dyserythropoietic Anemia Type 4 | Gastric Atrophy | Dyslipidemia | DRESS Syndrome | Tremor | Systemic Mastocytosis | Mitochondrial Cytopathy | Light Chain Amyloidosis | Acute Myeloid Leukemia | Retinoblastoma | Thrombasthenia | Nemaline Myopathy | Acute Generalized Exanthematous Pustulosis | Epidermolysis Bullosa Simplex, Localized | Acute Coronary Syndrome | Sleep Apnea, Central | Tay-Sachs Disease | Intracranial Hypertension | Arteriosclerosis | Gastroenteritis, Eosinophilic | Osteopetrosis | Heterotopic Ossification | Autosomal Recessive Spastic Paraplegia Type 35 | Pseudohermaphroditism | Calcium Pyrophosphate Deposition Disease | Hodgkin Lymphoma | ACTH-independent Macronodular Adrenal Hyperplasia | Primary Aldosteronism | Tricho-hepato-enteric Syndrome | Sarcoma, Alveolar Soft Part | Trimethylaminuria | Congenital Muscular Dystrophy | Charcot-Marie-Tooth Disease Type 2E | Myofibromatosis | Addison Disease | Gaze Palsy, Familial Horizontal, With Progressive Scoliosis, 2 | Anosmia, Congenital | Spinocerebellar Ataxia | Peyronie's Disease | Congestive Heart Failure | Tonsillitis | Myopathy | Anodontia | Metabolic Syndrome | Protein S Deficiency | Glomerulonephritis | Sturge-Weber Syndrome | Hereditary Elliptocytosis | Zellweger Syndrome | Niemann-Pick Disease, Type B | Glycogen Storage Disease Type 0, Muscle | Cold-induced Sweating Syndrome | Generalized Epilepsy With Febrile Seizures Plus | Microcephaly | Van Der Knaap Disease | Mabry Syndrome | Vitelliform Macular Dystrophy | Dysplastic Nevus | PASLI Disease | Nemaline Myopathy 8 | Keratoconus | Stroke, Hemorrhagic | HIBCH Deficiency | Thyroid Hormone Resistance | Cysticercosis | Peripheral T-cell Lymphoma | Polymicrogyria | Scoliosis | Spinocerebellar Ataxia Type 31 | Keratosis, Actinic | Pyelonephritis | Macular Corneal Dystrophy Type 1 | 3-M Syndrome | Optic Neuropathy, Anterior Ischemic | DEND Syndrome | Pulmonary Vein Stenosis | Prune Belly Syndrome | Cartilage Disorders | Crouzon Syndrome With Acanthosis Nigricans | Blau Syndrome | Oculocutaneous Albinism Type 1 | Hemosiderosis | Autoimmune Interstitial Lung, Joint, And Kidney Disease | Cutaneous Mastocytosis | Hyperthyroidism | Hereditary Sensory Neuropathy Type 1 | Guanidinoacetate Methyltransferase Deficiency | Pseudohypoparathyroidism Type 1C | Myosin Storage Myopathy | Hereditary Mixed Polyposis Syndrome | Gilbert Syndrome | Mucolipidosis | Donnai-Barrow Syndrome | Oculodentodigital Dysplasia | Alopecia | Measles | Malonyl-CoA Decarboxylase Deficiency | Iron Metabolism Disorders | Agranulocytosis | Chronic Granulomatous Disease, X-linked | Paroxysmal Nocturnal Hemoglobinuria | Bronchiolitis | Seborrheic Dermatitis | Adenomatoid Tumor | Cluster Headache | Carbohydrate Metabolism Disorders | Hypertrophic Osteoarthropathy, Primary, Autosomal Recessive 1 | Peeling Skin Syndrome, Acral Type | Neurocutaneous Syndromes | Pseudomyxoma Peritonei | Hepatorenal Syndrome | Chromosome 5q Deletion Syndrome | Syncope | Irritable Bowel Syndrome | Scapuloperoneal Myopathy, X-linked Dominant | Gyrate Atrophy Of The Choroid And Retina | Alagille Syndrome | Vascular Calcification | Sengers Syndrome | Histiocytosis | LEOPARD Syndrome | Corneal Edema | Progressive Familial Intrahepatic Cholestasis Type 3 | Ischemia | Primary Familial Brain Calcification | Depression | Mitochondrial DNA Depletion Syndrome, Hepatocerebral Form | Situs Inversus | Ependymoma | Crimean-Congo Hemorrhagic Fever | Hyperekplexia | Multiple Congenital Anomalies-hypotonia-seizures Syndrome 2 | Chromosome 17q21.31 Deletion Syndrome | Sclerosing Cholangitis | Holoprosencephaly | Amelogenesis Imperfecta | Phenylketonuria II | Acute Anterior Uveitis | Lattice Corneal Dystrophy | Colitis, Lymphocytic | Glaucoma, Congenital | Pituitary Stalk Interruption Syndrome | Carcinoma In Situ | Usher Syndrome Type II | Neurodermatitis | Megaloblastic Anemia | Diastrophic Dysplasia | Partington Syndrome | Lymphoma Lymphoblastic | Familial Partial Lipodystrophy | Vitamin A Deficiency | Neurofibroma, Plexiform | Blood Protein Disorders | Hyperinsulinemia | Dystonia Musculorum Deformans | Hereditary Sensory And Autonomic Neuropathy | Muscle Wasting | Lafora Disease | Hypotrichosis | Long QT Syndrome Type 3 | Thrombocythemia, Essential | Osteomalacia | Glycogen Storage Disease Type 0 | Thalassemia | Schindler Disease | Herpes Genitalis | Alzheimer Disease, Late Onset | Myeloid Leukemia | Methylmalonic Aciduria And Homocystinuria, CblC Type | Hypolipoproteinemia | Endometrial Hyperplasia | Autosomal Recessive Spastic Paraplegia Type 75 | Myositis | Myelitis, Transverse | Hyperbilirubinemia, Neonatal | Shprintzen-Goldberg Syndrome | D-2-Hydroxyglutaric Aciduria | L-2-Hydroxyglutaric Aciduria | Anorchia | Distal Spinal Muscular Atrophy | C3 Glomerulopathy | Palmoplantar Keratoderma | CDKL5 Deficiency Disorder | Pierson Syndrome | Keratoconjunctivitis | Carey-Fineman-Ziter Syndrome | Myasthenia Gravis | Pulmonary Alveolar Microlithiasis | Tibial Muscular Dystrophy | Pachyonychia Congenita | Graves Disease | Anal Fissure | Periventricular Leukomalacia | Lymphedema | Hereditary Multiple Exostoses | Esthesioneuroblastoma | Oguchi Disease-2 | Fibromuscular Dysplasia | Alazami Syndrome | Lymphoma, B-cell | Intellectual Disability, Autosomal Dominant 5 | Charcot-Marie-Tooth Disease Type 4B1 | Congenital Primary Aphakia | Sporadic Inclusion Body Myositis | Li-Fraumeni Syndrome | Ureteropelvic Junction Obstruction | Rolandic Epilepsy | Maple Syrup Urine Disease | Aldosterone Synthase Deficiency | Meningeal Melanocytoma | Subcortical Band Heterotopia | Hyperlipidemia | Tuberculosis | Retinoschisis | Mesial Temporal Lobe Epilepsy With Hippocampal Sclerosis | CHARGE Syndrome | Heterotaxy | Papillon-Lefevre Syndrome | Endometritis | Ehlers-Danlos Syndrome | Behavioral Variant Of Frontotemporal Dementia | Prostatitis | DiGeorge Syndrome | Keratocystic Odontogenic Tumor | Extramammary Paget's Disease | Rhabdomyosarcoma, Embryonal | Keratosis, Seborrheic | Sarcoidosis | Conn Syndrome | Mumps | Ameloblastic Carcinoma | Hypereosinophilic Syndrome | Otitis Externa | Diabetes Type 2 | Hemophilia | Renal Oncocytoma | Marfan Syndrome | Ulcerative Colitis | Eating Disorder | Hemangioblastoma | Glucagonoma | Carotid Artery Disease | Cancer, Prostate | Spondyloepiphyseal Dysplasia Tarda, X-linked | Spinocerebellar Ataxia Type 10 | Constipation | Bronchiectasis | Leukodystrophies | Aicardi-Goutieres Syndrome | Pendred Syndrome | Pyruvate Decarboxylase Deficiency | Reticular Dysgenesis | Gardner Syndrome | Hepatoblastoma | Melanocytic Nevus | Rothmund-Thomson Syndrome | Fibrodysplasia Ossificans Progressiva | Hypoplastic Left Heart Syndrome | Cataract | Diffuse Intrinsic Pontine Glioma | Myhre Syndrome | Hepatitis D | Fibrillation, Atrial | Scleroderma | Heavy Chain Disease | Hyperferritinemia-cataract Syndrome | Seminoma | Chronic Granulomatous Disease | Ellis-Van Creveld Syndrome | Large Granular Lymphocytic Leukemia | T-cell Leukemia | Congenital Generalized Lipodystrophy | Nicotine Addiction | Prolactinoma | Bleeding Disorder Due To CalDAG-GEFI Deficiency | Schuurs-Hoeijmakers Syndrome | Diabetes Gestational | McCune-Albright Syndrome | Blepharo-cheilo-odontic Syndrome | Lymphangiomatosis | Carney-Stratakis Syndrome | Restless Legs Syndrome | Sclerosteosis 2 | Deafness, Dystonia, And Cerebral Hypomyelination | Cocaine-Related Disorders | Colitis, Collagenous | Lesch-Nyhan Syndrome | Neuronal Ceroid Lipofuscinosis | Kaposi Sarcoma | Spinal And Bulbar Muscular Atrophy | Wieacker-Wolff Syndrome | Cholestasis, Intrahepatic | Cryoglobulinemia | Idiopathic Multicentric Castleman Disease