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

CTD Diseases (CD): ARTHROGRYPOSIS, PERTHES DISEASE, AND UPWARD GAZE PALSY

(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:   Diseases [MESH:C] <25>
+ + + + 4:   Pathological Conditions, Signs and Symptoms [MESH:D013568] <4>(81|94) (88|48|16)
+ + + + 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)
+ + + + 4:   Signs and Symptoms [MESH:D012816] <38>(30|33) (33|13|1)
+ + + 3:   Musculoskeletal Diseases [MESH:D009140] <13>(29|36) (36|21|18)
+ + + 3:   Neurologic Manifestations [MESH:D009461] <26>(22|24) (25|9|1)
+ + + 3:   Eye Diseases [MESH:D005128] <31>(8|6) (9|6|7)
+ + + 3:   Pathologic Processes [MESH:D010335] <65>(45|54) (50|27|12)
+ + + 3:   Neuromuscular Diseases [MESH:D009468] <15>(23|23) (24|10|3)
+ + + 3:   Cranial Nerve Diseases [MESH:D003389] <17>(1|1) (1|0|0)
+ + + 3:   Congenital Abnormalities [MESH:D000013] <50>(37|46) (40|17|10)
+ + + 3:   Central Nervous System Diseases [MESH:D002493] <15>(53|44) (57|16|3)
+ + 2:   Bone Diseases [MESH:D001847] <34>(10|9) (12|6|4)
+ + 2:   Muscular Diseases [MESH:D009135] <78>(13|11) (13|5|1)
+ + 2:   Paralysis [MESH:D010243] <10>(0|1) (3|2|1)
+ + 2:   Musculoskeletal Abnormalities [MESH:D009139] <30>(9|16) (12|4|4)
+ + 2:   Necrosis [MESH:D009336] <6>(9|6) (10|2|0)
+ + 2:   Joint Diseases [MESH:D007592] <43>(6|9) (8|6|2)
+ + 2:   Ocular Motility Disorders [MESH:D015835] <24>(0|0) (0|0|0)
+ 1:   Osteonecrosis [MESH:D010020] <5>(0|0) (0|0|0)
+ 1:   Ophthalmoplegia [MESH:D009886] <35>(0|0) (0|0|0)
+ 1:   Arthrogryposis [MESH:D001176] <69>(3|3) (3|1|0)
0:   ARTHROGRYPOSIS, PERTHES DISEASE, AND UPWARD GAZE PALSY [OMIM:614262](0|0) (0|0|0)