Disease Browser
Parent Node: Calcinosis (D002114) ..Starting node .. Vascular Calcification (D061205) Child Nodes:
........Arterial calcification of infancy (C537440) ........Monckeberg Medial Calcific Sclerosis (D050380) ........Singleton Merten syndrome (C537343) Sister Nodes: ..Aortic Valve, Calcification of (C562942) 1 ..BAND-LIKE CALCIFICATION WITH SIMPLIFIED GYRATION AND POLYMICROGYRIA (OMIM:251290) ..Baraitser Brett Piesowicz syndrome (C537905) ..Basal ganglia calcification, idiopathic 2 (C537657) ..Berry Aneurysm, Cirrhosis, Pulmonary Emphysema, and Cerebral Calcification (C565905) ..Calcific Aortic Disease with Immunologic Abnormalities, Familial (C566182) ..Calcification of Joints and Arteries (C565891) ..Calciphylaxis (D002115) ..Cardiomyopathy, fatal fetal, due to myocardial calcification (C543241) ..Cerebroretinal Microangiopathy with Calcifications and Cysts (C567401) ..Choroid plexus calcification with mental retardation (C535357) ..Coronary Sclerosis, Medial, of Infancy (C565944) ..Craniosynostosis, Calcification of Basal Ganglia, and Facial Dysmorphism (C564241) ..CREST Syndrome (D017675) ..Diabetes Insipidus, Nephrogenic, with Mental Retardation and Intracerebral Calcification (C565632) ..Encephalopathy with Intracranial Calcification, Growth Hormone Deficiency, Microcephaly, and Retinal Degeneration (C565594) ..Epilepsy occipital calcifications (C535496) ..Facial Dysmorphism, Selective Tooth Agenesis, and Choroid Calcification (C567039) ..GREENBERG DYSPLASIA (OMIM:215140) ..HEMORRHAGIC DESTRUCTION OF THE BRAIN, SUBEPENDYMAL CALCIFICATION, AND CATARACTS (OMIM:613730) ..Hypophosphatemia, Renal, with Intracerebral Calcifications (C565478) ..Idiopathic basal ganglia calcification 1 (C536275) ..Idiopathic basal ganglia calcification, childhood onset (C536276) ..Keutel syndrome (C536167) ..Nephrocalcinosis (D009397) 6 ..Ossified Ear Cartilages (C563488) ..Osteomalacia, Sclerosing, with Cerebral Calcification (C564916) ..Piepkorn Karp Hickok syndrome (C535774) ..Primrose syndrome (C536420) ..Pulmonary Alveolar Microlithiasis (C562405) ..RAJAB SYNDROME (OMIM:613658) ..Rambaud Galian syndrome (C535283) ..Schofer Beetz Bohl syndrome (C535949) ..Spondylomegaepiphyseal Dysplasia With Upper Limb Mesomelia, Punctate Calcifications, And Deafness (C566507) ..Storm Syndrome (C566109) ..Tropical Calcific Pancreatitis (C564276) ..Tumoral Calcinosis, Hyperphosphatemic, Familial (C566870) ..Tumoral Calcinosis, Normophosphatemic, Familial (C566473) ..Vascular Calcification (D061205) 3 ..Whyte Murphy Fallon Sly syndrome (C536060) Human Disease MESH is developed by UMLS . Further data from MedGen , OMIM , CTD
Term ID: 11525
Name: Vascular Calcification
Definition: Deposition of calcium into the blood vessel structures. Excessive calcification of the vessels are associated with ATHEROSCLEROTIC PLAQUES formation particularly after MYOCARDIAL INFARCTION (see MONCKEBERG MEDIAL CALCIFIC SCLEROSIS) and chronic kidney diseases which in turn increase VASCULAR STIFFNESS.
Alternative IDs:
ParentIDs: MESH:D002114
TreeNumbers: C18.452.174.130.780
Synonyms: Calcifications, Vascular |Calcification, Vascular |Calcinoses, Vascular |Calcinosis, Vascular |Vascular Calcifications |Vascular Calcinoses |Vascular Calcinosis
Slim Mappings: Metabolic disease
Reference:
MedGen: D061205
MeSH: D061205
OMIM: Genes: Phenotypes Disease Causing ClinVar Variants