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Ontology Browser

Term:
Parent Terms Term With Siblings Child Terms
Aloi Tomasini Isaia Syndrome 
Bent Bone Dysplasia 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 
ONYCHODYSTROPHY, OSTEODYSTROPHY, IMPAIRED INTELLECTUAL DEVELOPMENT, AND SEIZURES 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 +   
A bone remodeling disease that has_material_basis_in impaired mineralization or calcification of bones before epiphyseal closure due to deficiency or impaired metabolism of vitamin D, phosphorus or calcium which results_in softening and deformity located_in bone. (DO)

Synonyms
Exact Synonyms: active rickets ;   rachitides ;   rachitis ;   vitamin D hydroxylation-deficient rickets
Primary IDs: MESH:D012279
Xrefs: EFO:0005583 ;   GARD:5700 ;   ICD10CM:E55.0 ;   NCI:C26878 ;   ORDO:289157
Definition Sources: http://en.wikipedia.org/wiki/Rickets "DO" "DO", http://www.mayoclinic.com/health/rickets/DS00813 "DO" "DO", http://www.nlm.nih.gov/medlineplus/ency/article/000344.htm "DO" "DO", http://www.umm.edu/ency/article/000344.htm "DO" "DO", https://en.wikipedia.org/wiki/Rickets#Types "DO" "DO", https://www.ncbi.nlm.nih.gov/pubmed/26365554 "DO" "DO"

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