Disease Browser
|
Parent Node: Calcinosis (D002114) | ..Starting node ..Calciphylaxis (D002115)
| Child Nodes:
|
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: | 1571 |
Name: | Calciphylaxis |
Definition: | Condition of induced systemic hypersensitivity in which tissues respond to appropriate challenging agents with a sudden local calcification. |
Alternative IDs: | |
ParentIDs: | MESH:D002114 |
TreeNumbers: | C18.452.174.130.186 |
Synonyms: | Calciphylaxes |Calciphylaxis, Idiopathic |Idiopathic Calciphylaxis |
Slim Mappings: | Metabolic disease |
Reference: |
MedGen: D002115
MeSH: D002115
OMIM:
Genes: | Phenotypes | | Disease Causing ClinVar Variants | |
|