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CTD Diseases (CD): Macrogyria, pseudobulbar palsy and mental retardation

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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:   Pathological Conditions, Signs and Symptoms [MESH:D013568] <4>(81|94) (88|48|16)
+ + + + 4:   Signs and Symptoms [MESH:D012816] <38>(30|33) (33|13|1)
+ + + + 4:   Diseases [MESH:C] <25>
+ + + 3:   Mental Disorders [MESH:D001523] <27>(22|26) (25|8|3)
+ + + 3:   Neurologic Manifestations [MESH:D009461] <26>(22|24) (25|9|1)
+ + + 3:   Nervous System Diseases [MESH:D009422] <27>(86|87) (91|33|8)
+ + 2:   Paralysis [MESH:D010243] <10>(0|1) (3|2|1)
+ + 2:   Central Nervous System Diseases [MESH:D002493] <15>(53|44) (57|16|3)
+ + 2:   Neurobehavioral Manifestations [MESH:D019954] <10>(5|5) (5|1|0)
+ + 2:   Neurodevelopmental Disorders [MESH:D065886] <17>(9|11) (12|5|2)
+ 1:   Pseudobulbar Palsy [MESH:D020828] <1>(0|0) (0|0|0)
+ 1:   Intellectual Disability [MESH:D008607] <521>(2|2) (2|1|0)
+ 1:   Brain Diseases [MESH:D001927] <55>(46|37) (50|14|2)
0:   Macrogyria, pseudobulbar palsy and mental retardation [MESH:C537722](0|0) (0|0|0)