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Disease Ontology (DO): limb-girdle muscular dystrophy

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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)
+ + + + + + + 7:   disease [DOID:4] <8>
+ + + + + + 6:   disease of anatomical entity [DOID:7] <12>(143|187) (147|103|58)
+ + + + + 5:   musculoskeletal system disease [DOID:17] <3>(29|42) (37|17|6)
+ + + + 4:   muscular disease [DOID:0080000] <2>(9|13) (12|7|3)
+ + + 3:   muscle tissue disease [DOID:66] <5>(8|12) (11|7|3)
+ + 2:   myopathy [DOID:423] <23>(6|9) (7|6|2)
+ 1:   muscular dystrophy [DOID:9884] <10>(1|4) (2|4|1)
0:   limb-girdle muscular dystrophy [DOID:11724] <2>(0|0) (0|0|0)
- 1:   autosomal recessive limb-girdle muscular dystrophy [DOID:0110274] <24>(0|0) (0|0|0)
- 1:   autosomal dominant limb-girdle muscular dystrophy [DOID:0110273] <7>(0|0) (0|0|0)