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

CTD Diseases (CD): Brachymesomelia renal syndrome

(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:   Female Urogenital Diseases and Pregnancy Complications [MESH:D005261] <2>(47|58) (50|27|10)
+ + + + 4:   Female Urogenital Diseases [MESH:D052776] <6>(41|50) (42|22|9)
+ + + + 4:   Male Urogenital Diseases [MESH:D052801] <7>(38|49) (38|20|8)
+ + + + 4:   Diseases [MESH:C] <25>
+ + + 3:   Genetic Diseases, Inborn [MESH:D030342] <75>(79|83) (83|37|18)
+ + + 3:   Musculoskeletal Diseases [MESH:D009140] <13>(29|36) (36|21|18)
+ + + 3:   Eye Diseases [MESH:D005128] <31>(8|6) (9|6|7)
+ + + 3:   Congenital, Hereditary, and Neonatal Diseases and Abnormalities [MESH:D009358] <5>(101|119) (108|51|28)
+ + + 3:   Urologic Diseases [MESH:D014570] <9>(21|21) (21|8|3)
+ + 2:   Corneal Diseases [MESH:D003316] <26>(0|0) (0|0|0)
+ + 2:   Kidney Diseases [MESH:D007674] <65>(18|16) (18|5|3)
+ + 2:   Eye Diseases, Hereditary [MESH:D015785] <88>(7|5) (8|5|6)
+ + 2:   Congenital Abnormalities [MESH:D000013] <50>(37|46) (40|17|10)
+ + 2:   Musculoskeletal Abnormalities [MESH:D009139] <30>(9|16) (12|4|4)
+ + 2:   Bone Diseases [MESH:D001847] <34>(10|9) (12|6|4)
+ 1:   Bone Diseases, Developmental [MESH:D001848] <89>(2|4) (2|4|3)
+ 1:   Corneal Dystrophies, Hereditary [MESH:D003317] <52>(0|0) (0|0|0)
+ 1:   Abnormalities, Multiple [MESH:D000015] <389>(12|10) (12|4|3)
+ 1:   Craniofacial Abnormalities [MESH:D019465] <223>(3|9) (6|1|1)
+ 1:   Kidney Diseases, Cystic [MESH:D052177] <36>(0|1) (0|0|0)
0:   Brachymesomelia renal syndrome [MESH:C537096](0|0) (0|0|0)