| Disease Browser
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Parent Node:
 Calcium Metabolism Disorders (D002128) |
..Starting node
.. Calcinosis (D002114)
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Child Nodes:
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........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) |
Sister Nodes: |
..Calcinosis (D002114) 50
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..Decalcification, Pathologic (D003649) 1
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..Hypercalcemia (D006934) 10
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..Hypocalcemia (D006996) 5
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..Hypouricemia, Hypercalcinuria, and Decreased Bone Density (C565475)
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..Meier Blumberg Imahorn syndrome (C536148)
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..Pseudohypoparathyroidism (D011547) 6
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..Rickets (D012279) 16
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Human Disease MESH is developed by UMLS.
Further data from MedGen, OMIM, CTD
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