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Disease Ontology (DO): corneal disease

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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)
+ + + + + + 6:   disease [DOID:4] <8>
+ + + + + 5:   disease of anatomical entity [DOID:7] <12>(143|187) (147|103|58)
+ + + + 4:   nervous system disease [DOID:863] <11>(51|61) (54|28|13)
+ + + 3:   sensory system disease [DOID:0050155] <2>(16|13) (17|5|2)
+ + 2:   eye and adnexa disease [DOID:1492] <3>(13|11) (14|5|2)
+ 1:   eye disease [DOID:5614] <34>(13|11) (14|5|2)
0:   corneal disease [DOID:10124] <17>(0|2) (0|0|0)
- 1:   keratitis [DOID:4677] <9>(0|0) (0|0|0)
- 1:   corneal degeneration [DOID:1237] <7>(0|0) (0|0|0)
- 1:   corneal dystrophy [DOID:2566] <5>(0|0) (0|0|0)
- 1:   corneal edema [DOID:11030] <4>(0|1) (0|0|0)
- 1:   corneal deposit [DOID:11547] <3>(0|0) (0|0|0)
- 1:   keratoconus [DOID:10126] <2>(0|0) (0|0|0)
- 1:   pterygium [DOID:0002116] <2>(0|0) (0|0|0)
- 1:   sclerocornea [DOID:0060252] <1>(0|0) (0|0|0)
- 1:   Bowman's membrane folds or rupture [DOID:11552](0|0) (0|0|0)
- 1:   Peters anomaly [DOID:0060673](0|0) (0|0|0)
- 1:   cornea plana [DOID:0060287](0|0) (0|0|0)
- 1:   corneal argyrosis [DOID:13447](0|0) (0|0|0)
- 1:   corneal ectasia [DOID:1436](0|0) (0|0|0)
- 1:   corneal staphyloma [DOID:12753](0|0) (0|0|0)
- 1:   keratopathy [DOID:2283](0|1) (0|0|0)
- 1:   megalocornea [DOID:0060305](0|0) (0|0|0)
- 1:   pseudopterygium [DOID:11028](0|0) (0|0|0)


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Family

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SCOP termFDR (all)Annotation (direct or inherited)
Ngr ectodomain-like0.0008107Direct
Transforming growth factor (TGF)-beta0.008565Inherited


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