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CTD Diseases (CD): Pointer syndrome

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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)
+ + + 3:   Musculoskeletal Diseases [MESH:D009140] <13>(29|36) (36|21|18)
+ + + 3:   Diseases [MESH:C] <25>
+ + + 3:   Congenital, Hereditary, and Neonatal Diseases and Abnormalities [MESH:D009358] <5>(101|119) (108|51|28)
+ + 2:   Mental Disorders [MESH:D001523] <27>(22|26) (25|8|3)
+ + 2:   Musculoskeletal Abnormalities [MESH:D009139] <30>(9|16) (12|4|4)
+ + 2:   Bone Diseases [MESH:D001847] <34>(10|9) (12|6|4)
+ + 2:   Congenital Abnormalities [MESH:D000013] <50>(37|46) (40|17|10)
+ 1:   Limb Deformities, Congenital [MESH:D017880] <114>(3|4) (3|1|2)
+ 1:   Craniofacial Abnormalities [MESH:D019465] <223>(3|9) (6|1|1)
+ 1:   Feeding and Eating Disorders [MESH:D001068] <13>(0|0) (0|0|0)
+ 1:   Bone Diseases, Developmental [MESH:D001848] <89>(2|4) (2|4|3)
+ 1:   Abnormalities, Multiple [MESH:D000015] <389>(12|10) (12|4|3)
0:   Pointer syndrome [MESH:C536323](0|0) (0|0|0)