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CTD Diseases (CD): Hemiplegia

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Root: CD Hierarchy (CTD diseases from Comparative Toxicogenomics Database)

Shortest distance to current term
(+ for parents, - for children)
CD term [CD ID] <#Children> #Domains
(Superfamily|Family)
#Supra-domain
(Single|Duplex|Triple)
+ + + + + 5:   Diseases [MESH:C] <25>
+ + + + 4:   Pathological Conditions, Signs and Symptoms [MESH:D013568] <4>(81|94) (88|48|16)
+ + + 3:   Nervous System Diseases [MESH:D009422] <27>(86|87) (91|33|8)
+ + + 3:   Signs and Symptoms [MESH:D012816] <38>(30|33) (33|13|1)
+ + 2:   Neurologic Manifestations [MESH:D009461] <26>(22|24) (25|9|1)
+ 1:   Paralysis [MESH:D010243] <10>(0|1) (3|2|1)
0:   Hemiplegia [MESH:D006429] <1>(0|0) (0|0|0)
- 1:   Alternating hemiplegia of childhood [MESH:C536589](0|0) (0|0|0)