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Ontology Browser

Term:
Parent Terms Term With Siblings Child Terms
Aloi Tomasini Isaia Syndrome 
bone resorption disease +   
calcinosis +   
Chitty Hall Baraitser Syndrome 
congenital disorder of glycosylation type IIa  
fibrous dysplasia  
glycoproteinosis +   
hypercalcemia +   
Hypercalciuria +   
hyperostosis +   
Hypocalcemia +   
Hypophosphatemic Bone Disease 
Hypouricemia, Hypercalcinuria, and Decreased Bone Density 
Kaler Garrity Stern Syndrome 
osteomalacia +   
osteoporosis +   
osteosclerosis +   
Panostotic Fibrous Dysplasia 
Pathologic Bone Demineralization +  
Pathologic Decalcification +  
progressive osseous heteroplasia  
pseudohypoparathyroidism +   
renal hypomagnesemia 5 with ocular involvement  
Revesz syndrome  
rickets +   
Disorders caused by interruption of BONE MINERALIZATION manifesting as OSTEOMALACIA in adults and characteristic deformities in infancy and childhood due to disturbances in normal BONE FORMATION. The mineralization process may be interrupted by disruption of VITAMIN D; PHOSPHORUS; or CALCIUM homeostasis, resulting from dietary deficiencies, or acquired, or inherited metabolic, or hormonal disturbances.

Synonyms
Exact Synonyms: Rachitides ;   Rachitis ;   active rickets ;   vitamin D hydroxylation-deficient rickets ;   vitamin D-dependent rickets
Primary IDs: MESH:D012279 ;   RDO:0006473
Xrefs: GARD:5700 ;   ICD10CM:E55.0 ;   ICD9CM:268.0 ;   NCI:C26878 ;   ORDO:289157
Definition Sources: http://en.wikipedia.org/wiki/Rickets "DO", http://www.mayoclinic.com/health/rickets/DS00813 "DO", http://www.nlm.nih.gov/medlineplus/ency/article/000344.htm "DO", http://www.umm.edu/ency/article/000344.htm "DO", https://en.wikipedia.org/wiki/Rickets#Types "DO", https://www.ncbi.nlm.nih.gov/pubmed/26365554 "DO", MESH:D012279

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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.