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Disease Ontology (DO): mesenchymal cell neoplasm

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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> #Domains
(Superfamily|Family)
#Supra-domain
(Single|Duplex|Triple)
+ + + + 4:   disease [DOID:4] <8>
+ + + 3:   disease of cellular proliferation [DOID:14566] <3>(123|191) (129|118|56)
+ + 2:   cancer [DOID:162] <2>(115|181) (120|113|54)
+ 1:   cell type cancer [DOID:0050687] <11>(23|40) (25|27|17)
0:   mesenchymal cell neoplasm [DOID:3350] <7>(0|0) (0|0|0)
- 1:   epithelioid sarcoma [DOID:6193] <4>(0|0) (0|0|0)
- 1:   parachordoma [DOID:2647] <1>(0|0) (0|0|0)
- 1:   amyloid tumor [DOID:6755](0|0) (0|0|0)
- 1:   congenital granular cell tumor [DOID:8303](0|0) (0|0|0)
- 1:   inflammatory myofibroblastic tumor [DOID:0050905](0|0) (0|0|0)
- 1:   nonossifying fibromyxoid tumor [DOID:8305](0|0) (0|0|0)
- 1:   ossifying fibromyxoid tumor [DOID:2685](0|0) (0|0|0)