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CTD Diseases (CD): Alopecia, epilepsy, pyorrhea, mental subnormality

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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>
+ + + + + 5:   Skin and Connective Tissue Diseases [MESH:D017437] <2>(38|43) (41|28|20)
+ + + + 4:   Skin Diseases [MESH:D012871] <71>(31|34) (31|22|11)
+ + + + 4:   Nervous System Diseases [MESH:D009422] <27>(86|87) (91|33|8)
+ + + + 4:   Signs and Symptoms [MESH:D012816] <38>(30|33) (33|13|1)
+ + + + 4:   Congenital, Hereditary, and Neonatal Diseases and Abnormalities [MESH:D009358] <5>(101|119) (108|51|28)
+ + + 3:   Musculoskeletal Diseases [MESH:D009140] <13>(29|36) (36|21|18)
+ + + 3:   Congenital Abnormalities [MESH:D000013] <50>(37|46) (40|17|10)
+ + + 3:   Pathological Conditions, Signs and Symptoms [MESH:D013568] <4>(81|94) (88|48|16)
+ + + 3:   Neurologic Manifestations [MESH:D009461] <26>(22|24) (25|9|1)
+ + + 3:   Central Nervous System Diseases [MESH:D002493] <15>(53|44) (57|16|3)
+ + + 3:   Hair Diseases [MESH:D006201] <49>(3|2) (3|1|1)
+ + + 3:   Mental Disorders [MESH:D001523] <27>(22|26) (25|8|3)
+ + 2:   Hypotrichosis [MESH:D007039] <27>(1|1) (1|1|1)
+ + 2:   Pathological Conditions, Anatomical [MESH:D020763] <32>(8|9) (9|3|0)
+ + 2:   Brain Diseases [MESH:D001927] <55>(46|37) (50|14|2)
+ + 2:   Neurobehavioral Manifestations [MESH:D019954] <10>(5|5) (5|1|0)
+ + 2:   Neurodevelopmental Disorders [MESH:D065886] <17>(9|11) (12|5|2)
+ + 2:   Musculoskeletal Abnormalities [MESH:D009139] <30>(9|16) (12|4|4)
+ 1:   Alopecia [MESH:D000505] <57>(0|0) (0|0|0)
+ 1:   Epilepsy [MESH:D004827] <53>(8|8) (8|2|0)
+ 1:   Intellectual Disability [MESH:D008607] <521>(2|2) (2|1|0)
+ 1:   Craniofacial Abnormalities [MESH:D019465] <223>(3|9) (6|1|1)
0:   Alopecia, epilepsy, pyorrhea, mental subnormality [MESH:C537057](0|0) (0|0|0)