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CTD Diseases (CD): Kennerknecht Vogel 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)
+ + + + + + 6:   Female Urogenital Diseases and Pregnancy Complications [MESH:D005261] <2>(47|58) (50|27|10)
+ + + + + + 6:   Congenital, Hereditary, and Neonatal Diseases and Abnormalities [MESH:D009358] <5>(101|119) (108|51|28)
+ + + + + 5:   Male Urogenital Diseases [MESH:D052801] <7>(38|49) (38|20|8)
+ + + + + 5:   Female Urogenital Diseases [MESH:D052776] <6>(41|50) (42|22|9)
+ + + + + 5:   Congenital Abnormalities [MESH:D000013] <50>(37|46) (40|17|10)
+ + + + + 5:   Endocrine System Diseases [MESH:D004700] <18>(19|28) (22|15|10)
+ + + + 4:   Gonadal Disorders [MESH:D006058] <6>(5|4) (5|1|0)
+ + + + 4:   Urogenital Abnormalities [MESH:D014564] <52>(3|3) (3|1|0)
+ + + 3:   Disorders of Sex Development [MESH:D012734] <8>(2|2) (2|0|0)
+ + + 3:   Diseases [MESH:C] <25>
+ + 2:   Disorder of Sex Development, 46,XY [MESH:D058490] <17>(0|0) (0|0|0)
+ + 2:   Musculoskeletal Diseases [MESH:D009140] <13>(29|36) (36|21|18)
+ + 2:   Gonadal Dysgenesis [MESH:D006059] <9>(0|0) (0|0|0)
+ 1:   Gonadal Dysgenesis, 46,XY [MESH:D006061] <21>(0|0) (0|0|0)
+ 1:   Bone Diseases [MESH:D001847] <34>(10|9) (12|6|4)
0:   Kennerknecht Vogel syndrome [MESH:C537019](0|0) (0|0|0)