Vascular Calcification

About the Disease
Arterial Calcification, Generalized, of Infancy, 1, also known as idiopathic infantile arterial calcification, is related to arterial calcification, generalized, of infancy, 2 and pseudoxanthoma elasticum. An important gene associated with Arterial Calcification, Generalized, of Infancy, 1 is ENPP1 (Ectonucleotide Pyrophosphatase/Phosphodiesterase 1). The drugs Phylloquinone and Rivaroxaban have been mentioned in the context of this disorder. Affiliated tissues include heart, kidney and bone, and related phenotypes are short stature and hypophosphatemic rickets

Common Targets
GPR31 | CASR | G5743 | VKORC1 | VDR | DPP4 | MYORG | FDPS | CTH | ELN | IFIH1 | NT5E | PTPN4 | ALPI | SLC34A2 | BMPR1A | KAT2B | ALPL | CALU

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

Other Diseases

FG Syndrome | CHARGE Syndrome | Insulinoma | Spasticity | Meningeal Melanocytoma | Meningococcal Infections | Charcot-Marie-Tooth Disease Axonal Type 2N | Congenital Hypofibrinogenemia | Phosphoenolpyruvate Carboxykinase Deficiency, Cytosolic | Progressive Familial Intrahepatic Cholestasis Type 3 | Swine Influenza | Cutis Laxa | Keratoconus | Polymicrogyria | Cysticercosis | Alagille Syndrome | Hemolytic Uremic Syndrome, Atypical | Chronic Leukemia | Glomerulonephritis, Membranous | Contact Dermatitis | Bacterial Meningitis | Intermittent Explosive Disorder | Demyelinating Diseases | Pneumonia, Bacterial | Epicondylitis | Amyotrophic Lateral Sclerosis | Sick Sinus Syndrome | Carcinoma, Small Cell | Coronary Artery Disease | Keratocystic Odontogenic Tumor | Pyruvate Carboxylase Deficiency Disease | Fahr Disease | Familial Hyperaldosteronism | Congenital Dyserythropoietic Anemia Type 4 | Headache | Echinococcosis | Hypohidrotic Ectodermal Dysplasia | Whipple's Disease | Progressive Osseous Heteroplasia | Zygomycosis | Leukodystrophies | Hypobetalipoproteinemias | Neuromuscular Disorders | Keratitis-ichthyosis-deafness Syndrome | Poikiloderma With Neutropenia | Cerebellar Ataxia, Cayman Type | Leukocyte Adhesion Deficiency Type 1 | Myofibrillar Myopathy | Hepatitis, Alcoholic | Yellow Fever | Osteogenesis Imperfecta Type I | Pseudohypoparathyroidism Type 1B | Microcephalic Primordial Dwarfism | Pemphigus Foliaceus | VEXAS Syndrome | Myositis, Focal | Hepatopulmonary Syndrome | Plasma Cell Leukemia | Li-Fraumeni Syndrome | Traboulsi Syndrome | Basal Ganglia Disease, Biotin-responsive | Extramammary Paget's Disease | Dubin-Johnson Syndrome | Hereditary Mixed Polyposis Syndrome | Hypermetropia | Autism Spectrum Disorders | Dysmorphophobia | Dermatitis Herpetiformis | Veno-occlusive Disease | Moyamoya Disease | Ureteropelvic Junction Obstruction | Adenosine Deaminase 2 Deficiency | Ocular Hypertension | Agnathia-Otocephaly Complex | Schindler Disease | Chordoid Glioma | Intestinal Hypomagnesemia 1 | Amyotrophic Lateral Sclerosis-parkinsonism-dementia Complex | Paracoccidioidomycosis | Intestinal Obstruction | Renal Tubular Acidosis | Angiomyolipoma | Methemoglobinemia | Leiomyosarcoma | Cannabis Abuse | Papillon-Lefevre Syndrome | Glioblastoma Multiforme | Usher Syndrome | GM2-gangliosidosis AB Variant | Mitochondrial DNA Depletion Syndrome 13 | Kidney Stones | Ocular Albinism Type 1 | Melanocytic Nevus | Mitochondrial DNA Depletion Syndrome, Myopathic Form | Congenital Adrenal Hyperplasia | Obsessive-compulsive Disorder | Chronic Myeloid Leukemia | Hemoglobinopathies | Androgenic Alopecia | Ehlers-Danlos Syndrome | Epithelial-myoepithelial Carcinoma | Osteogenesis Imperfecta Type VI | Spinocerebellar Ataxia Type 6 | Thymoma, Malignant | Varices | Cramp Fasciculation Syndrome | Congenital Muscular Dystrophy | Thalassemia | Autoimmune Disease | Ventricular Septal Defect | Orthostatic Intolerance | Spondyloepiphyseal Dysplasia Tarda, X-linked | Hyperinsulinemic Hypoglycemia | Succinic Semialdehyde Dehydrogenase Deficiency | Pituitary Disorders | Genitopatellar Syndrome | Colitis, Lymphocytic | Liver Failure | Pigment Dispersion Syndrome | Familial Mediterranean Fever | Colitis, Microscopic | Twin-to-twin Transfusion Syndrome | Gingivitis | Proteus Syndrome | Eczema | Liddle Syndrome | Acute Anterior Uveitis | DICER1 Syndrome | Language Disorders | Ileitis | Autoimmune Polyendocrinopathy Syndrome Type I | Diabetes Insipidus, Nephrogenic | Hemolytic Anemia | Beta-Propeller Protein-associated Neurodegeneration | Congenital Primary Aphakia | Coffin-Lowry Syndrome | Diabetes Insipidus, Neurogenic | Dysplastic Nevus | Pseudohermaphroditism | Aplasia Cutis Congenita | Neurodevelopmental Disorders | Prolymphocytic Leukemia | Sandhoff Disease | Acrodermatitis | Keratosis | Hypotrichosis Simplex | Congenital Adrenal Hyperplasia 1 | Sitosterolemia | Congenital Torticollis | Walker-Warburg Syndrome | Otopalatodigital Syndrome Type 2 | Lymphangioma | Aphasia | Torticollis | NGLY1 Deficiency | Sarcoidosis | T-cell Leukemia | Congenital Hereditary Endothelial Dystrophy Type I | DiGeorge Syndrome | Neuromyotonia | Hereditary Elliptocytosis | Endometriosis | Microcephalic Osteodysplastic Primordial Dwarfism, Type II | Myelodysplasia | Hyperandrogenemia | Tuberculosis | Hypertensive Retinopathy | Multiple Sulfatase Deficiency | Hemorrhage | Hypopigmentation | Oguchi Disease-2 | Vitreoretinal Degeneration, Snowflake Type | Retinal Degeneration | Azoospermia | 3-methylglutaconic Aciduria Type I | Binge Eating Disorder | Chromosome 16p11.2 Deletion Syndrome | Optic Neuropathy, Anterior Ischemic | Progressive Familial Intrahepatic Cholestasis Type 2 | Hypertension, Portal | Ophthalmia, Sympathetic | Lipid Storage Diseases | Iron Metabolism Disorders | Anuria | Pernicious Anemia | Peritonitis | Chloridorrhea, Congenital | Neuroleptic Malignant Syndrome | Ollier Disease | Cat Eye Syndrome | Carcinoid Tumor | Connective Tissue Disorders | Primary Ovarian Insufficiency | Schizencephaly | Mitochondrial DNA Depletion Syndrome, Hepatocerebral Form | Myasthenia Gravis | Skin Carcinoma | Spinocerebellar Ataxia Type 5 | Thrombotic Microangiopathy | Gastroschisis | Olmsted Syndrome | Polycystic Liver | Multicentric Carpotarsal Osteolysis Syndrome | Dengue Shock Syndrome | Histiocytic Sarcoma | Blastomycosis | Systemic Lupus Erythematosus | Common Variable Immunodeficiency | Haim-Munk Syndrome | Congenital Ichthyosiform Erythroderma | Ganglioneuroma | Borderline Personality Disorder | Nager Acrofacial Dysostosis | Urolithiasis | Spondylocostal Dysostosis | Argininosuccinic Aciduria | Inflammatory Bowel Disease | Goldenhar Syndrome | CEDNIK Syndrome | Hypotrichosis, Congenital, With Juvenile Macular Dystrophy | Renal Failure | Epidermodysplasia Verruciformis | Schaaf-Yang Syndrome | Smith-Kingsmore Syndrome | Arthrogryposis | Lymphoma Lymphoblastic | Sclerosteosis | Pseudohypoaldosteronism | Gastritis, Atrophic | Chiari Malformation Type I | Cirrhosis | Inflammatory Myopathy | Primrose Syndrome | Cholelithiasis | Tonsillitis | Nutrition Disorders | Tendinitis | Pathological Gambling | Encephalopathy, Ethylmalonic | Oligodendroglioma | Generalized Epilepsy And Paroxysmal Dyskinesia | Dysferlinopathy | Iron Deficiency Anemia | Facioscapulohumeral Muscular Dystrophy | Chronic Idiopathic Myelofibrosis | Localized Scleroderma | Hypertension, Renovascular | Osteonecrosis | Pseudomyxoma Peritonei | Open-angle Glaucoma | Intestinal Tuberculosis | Impetigo | Dyggve-Melchior-Clausen Disease | 3-hydroxy-3-methylglutaric Aciduria | Nijmegen Breakage Syndrome | Bipolar Disorder | Birt-Hogg-Dube Syndrome | Diabetic Nephropathy | Epidermolysis Bullosa Simplex | Trachoma | Addison Disease | Familial Male-limited Precocious Puberty | Spinocerebellar Ataxia Type 13 | Amyloidosis | Macular Corneal Dystrophy Type 1 | Absence Epilepsy | Crisponi Syndrome | Carotid Artery Disease | Measles | Thrombocytopenia | Cutaneous Angiosarcoma | Ovarian Hyperstimulation Syndrome | Pulverulent Zonular Cataract | Adenoma, Villous | Giant Cell Arteritis | McCune-Albright Syndrome | Cleidocranial Dysplasia | Fundus Albipunctatus | Pulmonary Alveolar Microlithiasis | Best Macular Dystrophy | Cryptosporidiosis | Acute Myeloid Leukemia | Cryptococcal Meningitis | Vestibular Disease | Medulloblastoma | Vitiligo | Epilepsy, Generalized | Arthropathy | Peyronie's Disease | Proteasome-associated Autoinflammatory Syndrome 2 | Charcot-Marie-Tooth Disease, Type 6 | Cellulitis | Achromatopsia | Neural Tube Defect | Pulmonary Veno-occlusive Disease | Lissencephaly 2 | Schizotypal Personality Disorder | Arthritis, Gouty | Mountain Sickness | Nicolaides-Baraitser Syndrome | Autism | Hypersomnia | Pseudohypoparathyroidism Type 1C | Congenital Tufting Enteropathy | IgA Deficiency | AIDS | Genee-Wiedemann Syndrome | Blue Nevus | Cardiomyopathy, Hypertrophic | Tetanus | Fanconi Syndrome | Aspartylglycosaminuria | Early Infantile Epileptic Encephalopathy 28 | Fucosidosis | Sengers Syndrome | Leukemia-lymphoma, Adult T-cell | Tricho-hepato-enteric Syndrome | Hypertensive Nephropathy | Corneal Neovascularization | Hyperkeratosis | Angiosarcoma | Schizoaffective Disorder | IMAGe Syndrome | Trichotillomania | Primary Cutaneous Amyloidosis | Spondylo-ocular Syndrome | Intermittent Claudication | Rosacea | Filariasis | Muscular Dystrophy | Graft-versus-host Disease | Endometritis | Niemann-Pick Disease | Primary Torsion Dystonia | Nephropathy | Primary Progressive Aphasia | Congestive Heart Failure | Diarrhea | Hypertension, Renal | GATA2 Deficiency | Phenylketonuria II | Rubinstein-Taybi Syndrome | X-linked Charcot-Marie-Tooth Disease | Microcephaly | Otitis Externa | Loeys-Dietz Syndrome Type 4 | Dystonia Musculorum Deformans | Juvenile Myelomonocytic Leukemia | Cocaine-Related Disorders | Aceruloplasminemia | Lipodystrophy | Klippel-Feil Syndrome | Pyruvate Dehydrogenase Deficiency | Restrictive Dermopathy | Macular Degeneration | Acquired Partial Lipodystrophy | Hennekam Lymphangiectasia-lymphedema Syndrome | Camptocormia | Metanephric Adenoma | Carcinoma In Situ | Hypohidrotic Ectodermal Dysplasia, X-linked | Primary Biliary Cholangitis | Adenosine Deaminase Deficiency | Atopic Dermatitis | Glucagonoma | Episodic Ataxia Type 1 | Gliosarcoma | Renal Tubular Dysgenesis | Osteoarthritis | Apraxia | Neuroblastoma | Eosinophilia | Acute Chest Syndrome | Fuchs Heterochromic Iridocyclitis | Anthrax | Tatton-Brown-Rahman Syndrome | Metabolic Diseases | Hyperprolactinemia | Rhabdomyosarcoma, Alveolar | Conduct Disorder | Pelvic Inflammatory Disease | Marinesco-Sjogren Syndrome | Purpura, Thrombotic Thrombocytopenic | Primary Sclerosing Cholangitis | Hypertrophic Osteoarthropathy, Primary, Autosomal Recessive 1 | Chylothorax, Congenital | Carbohydrate Metabolism Disorders | Osteogenesis Imperfecta Type V | Rift Valley Fever | Hereditary Multiple Exostoses | Pure Red Cell Aplasia | C3 Glomerulopathy | Pleomorphic Xanthoastrocytoma | Nemaline Myopathy 10 | Methylmalonic Aciduria And Homocystinuria, CblC Type | Von Hippel-Lindau Disease | Aldosteronism | Bicuspid Aortic Valve | Chondroma | Neurofibromatosis