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Disease Ontology (DO): calcinosis

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Root: DO Hierarchy (disease ontology from University of Maryland)

Shortest distance to current term (+ for parents, - for children) DO term [DO ID] <#Children> (#SF|#FA) #Supra-domain
(Single|Duplex|Triple)
+ + + + + 5:   disease [DOID:4] <8>
+ + + + 4:   disease of metabolism [DOID:0014667] <2>(22|34) (27|12|5)
+ + + 3:   acquired metabolic disease [DOID:0060158] <8>(14|21) (16|10|5)
+ + 2:   mineral metabolism disease [DOID:0050032] <4>(0|0) (0|0|0)
+ 1:   calcium metabolism disease [DOID:10575] <3>(0|0) (0|0|0)
0:   calcinosis [DOID:182] <5>(0|0) (0|0|0)
- 1:   calciphylaxis [DOID:4734](0|0) (0|0|0)
- 1:   diffuse idiopathic skeletal hyperostosis [DOID:6652](0|0) (0|0|0)
- 1:   hyperphosphatemic familial tumoral calcinosis [DOID:0111063](0|0) (0|0|0)
- 1:   nephrocalcinosis [DOID:12679](0|0) (0|0|0)
- 1:   normophosphatemic familial tumoral calcinosis [DOID:0080170](0|0) (0|0|0)