Cantu Syndrome

About the Disease
Cantu Syndrome, also known as hypertrichotic osteochondrodysplasia, is related to cardiomyopathy, dilated, 1o and patent ductus arteriosus 1. An important gene associated with Cantu Syndrome is ABCC9 (ATP Binding Cassette Subfamily C Member 9), and among its related pathways/superpathways are Transmission across Chemical Synapses and Potassium Channels. Affiliated tissues include bone, heart and skin, and related phenotypes are coarse facial features and thick vermilion border

Common Targets
ABCC9

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

Other Diseases

Carcinoma, Signet Ring Cell | Cold-induced Sweating Syndrome | Congenital Lipoid Adrenal Hyperplasia | Schizophrenia, Paranoid | Tonsillitis | Patent Foramen Ovale | Psoriasis | Chromosome 8q21.11 Deletion Syndrome | Restless Legs Syndrome | Vogt-Koyanagi-Harada Syndrome | Arthritis | Analgesia | Spinocerebellar Ataxia Type 10 | Snyder-Robinson Syndrome | Gaze Palsy, Familial Horizontal, With Progressive Scoliosis, 2 | Ichthyosis | Trichothiodystrophy | Focal Cortical Dysplasia Type 2 | Cancer, Brain | Babesiosis | Hypertensive Nephropathy | Primary Hyperoxaluria Type 3 | Endometritis | Iron Deficiency Anemia | Mabry Syndrome | LMNA-related Congenital Muscular Dystrophy | Opisthorchiasis | Zellweger Syndrome | Achondrogenesis | Lathosterolosis | Celiac Disease | Papilloma | Anti-NMDA Receptor Encephalitis | Amblyopia | Osteosarcoma | Retinopathy Of Prematurity | Congenital Bile Acid Synthesis Defect | Stickler Syndrome | Jacobsen Syndrome | Multiple Sclerosis, Chronic Progressive | Nutrition Disorders | Aspergillosis | Pseudoexfoliation Syndrome | Spinocerebellar Ataxia Type 17 | Cardiomyopathy, Hypertrophic | Bone Marrow Necrosis | Pontocerebellar Hypoplasia Type 7 | Peters-plus Syndrome | Pernicious Anemia | Tic Disorder | Cardiofaciocutaneous Syndrome | Chronic Lymphocytic Leukemia | Sarcoma, Alveolar Soft Part | Thrombophlebitis | Glanzmann Thrombasthenia | Carcinoma, Merkel Cell | Craniofacial Dysostosis | Cholera | Hypersensitivity Pneumonitis | Adenylosuccinate Lyase Deficiency | Oligospermia | Hereditary Folate Malabsorption | Hereditary Spherocytosis | Dementia, Vascular | Encephalopathy, Glycine | Retinal Coloboma | Retinitis | Coronary Heart Disease | Mandibuloacral Dysplasia With Type A Lipodystrophy | Postpoliomyelitis Syndrome | Keratosis, Actinic | Acrodermatitis Enteropathica | Primary Cutaneous Amyloidosis | Spondyloperipheral Dysplasia | Pneumoconiosis | Congenital Generalized Lipodystrophy | Sickle Cell Disease | Hypersensitivity | Epidermolysis Bullosa Simplex, Localized | Phosphoenolpyruvate Carboxykinase Deficiency, Cytosolic | Epidermolytic Ichthyosis, Annular | Inflammatory Myofibroblastic Tumor | Microcephalic Osteodysplastic Primordial Dwarfism, Type II | Leri Pleonosteosis | DNA Ligase IV Deficiency | Evans Syndrome | Purpura | Melanoma, Uveal | Osteogenesis Imperfecta Type II | Vitreoretinopathy, Proliferative | Acute Kidney Injury | Lewy Body Dementia | Ameloblastoma | Sleep Apnea, Obstructive | Benign Familial Pemphigus | Hypercalcemia | Cataplexy | KBG Syndrome | Multiple Congenital Anomalies-hypotonia-seizures Syndrome 2 | Rhabdomyosarcoma, Embryonal | Seizures-scoliosis-macrocephaly Syndrome | Alpha-1 Antitrypsin Deficiency | Erythematotelangiectatic Rosacea | Pseudohypoparathyroidism Type 1B | Long QT Syndrome Type 2 | Chromosome 16p11.2 Deletion Syndrome | Avellino Corneal Dystrophy | Neurofibroma, Plexiform | Proopiomelanocortin Deficiency | Presbyopia | Paternal Uniparental Disomy Of Chromosome 14 | Gastroenteritis | Pseudohermaphroditism | Epidermal Nevus Syndrome | Neurodegeneration With Brain Iron Accumulation | Primary Erythromelalgia | Keratitis | Anodontia | Polycystic Ovary Syndrome | Contact Dermatitis | Pilomatrix Carcinoma | Thrombosis | Palsy, Cerebral | Hypoalbuminemia | Dubin-Johnson Syndrome | Discoid Lupus Erythematosus | Beta-Propeller Protein-associated Neurodegeneration | Retinopathy, Diabetic | Mitochondrial DNA Depletion Syndrome, Hepatocerebral Form | Megaloblastic Anemia | Schamberg Disease | Benign Hereditary Chorea | Migraine | Osteogenesis Imperfecta Type I | Pyruvate Carboxylase Deficiency Disease | Atopy | Amyloidosis | Epiphyseal Chondrodysplasia, Miura Type | Sensory Neuropathy | Fibrillation, Atrial | Mitochondrial DNA Depletion Syndrome 13 | Sensory Ataxic Neuropathy, Dysarthria, And Ophthalmoparesis | Dysplastic Nevus | Niemann-Pick Disease, Type C | Dowling-Degos Disease | LEOPARD Syndrome | Keratoconus | REM Sleep Behavior Disorder | Progressive External Ophthalmoplegia | Meesmann Corneal Dystrophy | Meningioma | Retinal Vasculitis | Corneal Ulcer | Osteogenesis Imperfecta Type VI | Sleep Apnea, Central | Leukocyte Adhesion Deficiency | Camurati-Engelmann Disease | Spinocerebellar Ataxia Type 27 | Chronic Periodontitis | Primary Hyperoxaluria Type 1 | Goiter, Nodular | Hereditary Inclusion Body Myopathy | Wieacker-Wolff Syndrome | Oculocutaneous Albinism Type 2 | Ureteropelvic Junction Obstruction | Hepatitis, Alcoholic | Pemphigus Vulgaris | Ghosal Syndrome | Sialoadenitis | Keratoacanthoma | Cholangitis | Rhabdomyosarcoma | Hereditary Coproporphyria | Extramammary Paget's Disease | Chronic Thromboembolic Pulmonary Hypertension | Citrullinemia | Desmosterolosis | Keratitis-ichthyosis-deafness Syndrome | Trachoma | 5-oxoprolinase Deficiency | Vitelliform Macular Dystrophy | Adenosine Deaminase 2 Deficiency | Myocardial Infarction | Relapsing Polychondritis | Ataxia-ocular Apraxia 2 | Spondylo-megaepiphyseal-metaphyseal Dysplasia | Autism | Medulloblastoma | Fanconi Syndrome | Situs Inversus | Epilepsy, Generalized | Still Disease | Haim-Munk Syndrome | Spastic Paraplegia Type 7 | Gastritis | Arteriosclerosis | Bronchitis, Chronic | Osteopetrosis | Lattice Corneal Dystrophy Type 1 | Rift Valley Fever | Precocious Puberty | Pseudomyxoma Peritonei | Vitreoretinal Degeneration, Snowflake Type | Sandhoff Disease | Parkinsonism | Spinocerebellar Ataxia Type 1 | Diabetic Neuropathy | Corneal Dystrophy And Perceptive Deafness | Meningioma, Benign | Corneal Edema | Hypervalinemia | Neuroleptic Malignant Syndrome | Infertility | Calcium Pyrophosphate Deposition Disease | Carcinoid Syndrome | Seborrheic Dermatitis | Arteriovenous Malformations | Osteoglophonic Dysplasia | Erysipelas | Urea Cycle Disorder | Lupus Erythematosus | Chronic Neutrophilic Leukemia | Panic Disorder | Prediabetes | Cannabis Abuse | Macular Degeneration | Persistent Mullerian Duct Syndrome | Nephroblastoma | Acromicric Dysplasia | Neuromuscular Disorders | Acquired Partial Lipodystrophy | Fabry's Disease | Leber Congenital Amaurosis | Cardiomyopathy, Restrictive | Histoplasmosis | Otosclerosis | Peeling Skin Syndrome, Acral Type | Cancer, Skin | Sotos Syndrome | Polymyositis | Myelitis | Neuromyotonia | Congenital Diaphragmatic Hernia | Brooke-Spiegler Syndrome | Compartment Syndrome | Congenital Aniridia | Stargardt Disease | Renal Oncocytoma | Brugada Syndrome 1 | Hypocalcemia | Hyperbilirubinemia | Endometriosis | Scleroderma | Familial Exudative Vitreoretinopathy | Partington Syndrome | Genee-Wiedemann Syndrome | Adenoma, Villous | Genitopatellar Syndrome | Christianson Syndrome | Skin Papilloma | Incontinentia Pigmenti | Central Pain Syndrome | Constipation | Noonan Syndrome | Diabetes Insipidus, Nephrogenic | Lymphoproliferative Disorders | Oculocutaneous Albinism Type 1 | Cutaneous Angiosarcoma | Non-Hodgkin Lymphoma | Cavitary Optic Disc Anomalies | Waldenstrom Macroglobulinemia | Okihiro Syndrome | Microcephaly | Hepatitis, Chronic | Double Outlet Right Ventricle | Gastric Atrophy | Hamartoma | Mycosis Fungoides | Danon Disease | Bursitis | Scapuloperoneal Myopathy, X-linked Dominant | Periodic Limb Movement Disorder | Tyrosinemia | Autosomal Recessive Spastic Paraplegia Type 54 | Huntington's Disease | Focal Dermal Hypoplasia | Osteoporosis | Tendinitis | Colitis, Microscopic | Phenylketonuria | Autoimmune Hemolytic Anemia | Lactose Intolerance | Neurotoxicity | Blepharospasm | Familial Mediterranean Fever | Norrie Disease | Alkaptonuria | Optic Neuropathy | Charcot-Marie-Tooth Disease | Treacher Collins Syndrome | Fibromuscular Dysplasia | Lattice Corneal Dystrophy | Cerebral Cavernous Malformations | FG Syndrome | Aplasia Cutis Congenita | Cenani-Lenz Syndactyly Syndrome | Prolactinoma | Hemolytic Uremic Syndrome, Atypical | Diffuse Idiopathic Pulmonary Neuroendocrine Cell Hyperplasia | Greenberg Dysplasia | Vestibular Disease | Lipid Storage Myopathy | Prolymphocytic Leukemia | Multiple Sclerosis | T-cell Leukemia | Personality Disorders | Aarskog-Scott Syndrome | Antley-Bixler Syndrome | Adrenoleukodystrophy, X-linked | Porphyria, Variegate | Osteitis | Osteochondroma | Portal Vein Thrombosis | Acne | Stevens-Johnson Syndrome | Birt-Hogg-Dube Syndrome | Hypertrophy | Nephropathy | Frontotemporal Dementia With Amyotrophic Lateral Sclerosis | Enterocolitis, Necrotizing | Xeroderma Pigmentosum | Early Infantile Epileptic Encephalopathy | Albinism | Thrombasthenia | Anti-glomerular Basement Membrane Disease | Encephalocele | Anovulation | Intestinal Tuberculosis | Multiple Sulfatase Deficiency | Chondromyxoid Fibroma | Giant Cell Arteritis | Lentigo | Dysmorphophobia | Chronic Enteropathy Associated With SLCO2A1 Gene | Pancytopenia | Pancreatitis, Chronic | Ischemia | Purpura, Thrombotic Thrombocytopenic | Conjunctivitis | Krabbe Disease | Sclerosing Cholangitis | Acral Lentiginous Melanoma | Coronary Artery Disease | Chylothorax, Congenital | Schizencephaly | Hereditary Pyropoikilocytosis | Diastrophic Dysplasia | Hypophosphatemic Rickets With Hypercalciuria, Hereditary | Olmsted Syndrome | Hydrocephalus, Normal Pressure | Hypertension | IgA Nephropathy | Glycogen Storage Disease Type 1a | Ellis-Van Creveld Syndrome | Charcot-Marie-Tooth Disease Type 4D | Tremor | Macular Corneal Dystrophy | Tularemia | Holoprosencephaly | X-linked Sideroblastic Anemia | Oligoasthenoteratozoospermia | Martsolf Syndrome | Angiodysplasia | Hypolipoproteinemia | Takayasu's Arteritis | VACTERL Association | Pitt-Hopkins Syndrome | Diabetic Nephropathy | Niemann-Pick Disease, Type B | DICER1 Syndrome | Pericarditis | Spondylosis | Cystinosis | Facioscapulohumeral Muscular Dystrophy Type 2 | Conduct Disorder | Thyroid Hormone Resistance | Gardner Syndrome | Tangier Disease | Myelomeningocele | Infantile Nephropathic Cystinosis | Cardiac Arrest | Blepharitis | Chordoid Glioma | Inflammatory Joint Disease | Ocular Hypertension | Stuttering | Superficial Spreading Melanoma | Hyperinsulinemia | Scleritis | Enlarged Vestibular Aqueduct