dcGO - A comprehensive domain-centric ontology resource for post-genomic research on functions, phenotypes, diseases and more   
  
  

CTD Diseases (CD): Cortical Defects, Wormian Bones, and Dentinogenesis Imperfecta

(show info)

Jump to [ Top · Hierarchy · Annotations ]

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:   Congenital, Hereditary, and Neonatal Diseases and Abnormalities [MESH:D009358] <5>(101|119) (108|51|28)
+ + + + 4:   Congenital Abnormalities [MESH:D000013] <50>(37|46) (40|17|10)
+ + + + 4:   Stomatognathic Diseases [MESH:D009057] <7>(9|14) (12|8|4)
+ + + + 4:   Diseases [MESH:C] <25>
+ + + 3:   Tooth Diseases [MESH:D014076] <26>(0|0) (1|2|0)
+ + + 3:   Musculoskeletal Diseases [MESH:D009140] <13>(29|36) (36|21|18)
+ + + 3:   Stomatognathic System Abnormalities [MESH:D018640] <5>(1|2) (3|3|1)
+ + 2:   Bone Diseases [MESH:D001847] <34>(10|9) (12|6|4)
+ + 2:   Tooth Abnormalities [MESH:D014071] <53>(0|0) (1|2|0)
+ 1:   Bone Diseases, Developmental [MESH:D001848] <89>(2|4) (2|4|3)
+ 1:   Dentinogenesis Imperfecta [MESH:D003811] <6>(0|0) (0|0|0)
0:   Cortical Defects, Wormian Bones, and Dentinogenesis Imperfecta [MESH:C565734](0|0) (0|0|0)