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Disease Ontology (DO): pseudoretinitis pigmentosa

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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)
+ + + + + + + + + 9:   disease [DOID:4] <8>
+ + + + + + + + 8:   disease of anatomical entity [DOID:7] <12>(143|187) (147|103|58)
+ + + + + + + 7:   nervous system disease [DOID:863] <11>(51|61) (54|28|13)
+ + + + + + 6:   sensory system disease [DOID:0050155] <2>(16|13) (17|5|2)
+ + + + + 5:   eye and adnexa disease [DOID:1492] <3>(13|11) (14|5|2)
+ + + + 4:   eye disease [DOID:5614] <34>(13|11) (14|5|2)
+ + + 3:   retinal disease [DOID:5679] <20>(3|1) (4|2|1)
+ + 2:   retinal degeneration [DOID:8466] <8>(2|1) (3|2|1)
+ 1:   peripheral retinal degeneration [DOID:12161] <6>(0|0) (0|0|0)
0:   pseudoretinitis pigmentosa [DOID:12162](0|0) (0|0|0)