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CTD Diseases (CD): Massa Casaer Ceulemans 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)
+ + + + + 5:   Diseases [MESH:C] <25>
+ + + + 4:   Nervous System Malformations [MESH:D009421] <27>(7|9) (7|2|0)
+ + + + 4:   Nervous System Diseases [MESH:D009422] <27>(86|87) (91|33|8)
+ + + + 4:   Congenital, Hereditary, and Neonatal Diseases and Abnormalities [MESH:D009358] <5>(101|119) (108|51|28)
+ + + 3:   Congenital Abnormalities [MESH:D000013] <50>(37|46) (40|17|10)
+ + + 3:   Musculoskeletal Diseases [MESH:D009140] <13>(29|36) (36|21|18)
+ + + 3:   Malformations of Cortical Development [MESH:D054220] <26>(5|5) (5|2|0)
+ + + 3:   Neuromuscular Diseases [MESH:D009468] <15>(23|23) (24|10|3)
+ + 2:   Muscular Diseases [MESH:D009135] <78>(13|11) (13|5|1)
+ + 2:   Joint Diseases [MESH:D007592] <43>(6|9) (8|6|2)
+ + 2:   Malformations of Cortical Development, Group II [MESH:D054081] <4>(2|0) (2|0|0)
+ + 2:   Musculoskeletal Abnormalities [MESH:D009139] <30>(9|16) (12|4|4)
+ 1:   Arthrogryposis [MESH:D001176] <69>(3|3) (3|1|0)
+ 1:   Lissencephaly [MESH:D054082] <16>(1|0) (1|0|0)
0:   Massa Casaer Ceulemans syndrome [MESH:C536031](0|0) (0|0|0)