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CTD Diseases (CD): Macroepiphyseal dysplasia, McAlister Coe type

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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)
+ + + + 4:   Nutritional and Metabolic Diseases [MESH:D009750] <2>(51|55) (57|23|4)
+ + + 3:   Metabolic Diseases [MESH:D008659] <23>(49|55) (54|22|4)
+ + + 3:   Musculoskeletal Diseases [MESH:D009140] <13>(29|36) (36|21|18)
+ + + 3:   Diseases [MESH:C] <25>
+ + 2:   Skin and Connective Tissue Diseases [MESH:D017437] <2>(38|43) (41|28|20)
+ + 2:   Bone Diseases, Metabolic [MESH:D001851] <14>(0|0) (0|0|0)
+ + 2:   Bone Diseases [MESH:D001847] <34>(10|9) (12|6|4)
+ 1:   Skin Diseases [MESH:D012871] <71>(31|34) (31|22|11)
+ 1:   Osteoporosis [MESH:D010024] <19>(0|0) (0|0|0)
+ 1:   Bone Diseases, Developmental [MESH:D001848] <89>(2|4) (2|4|3)
0:   Macroepiphyseal dysplasia, McAlister Coe type [MESH:C537721](0|0) (0|0|0)