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CTD Diseases (CD): Keloid

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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:   Pathological Conditions, Signs and Symptoms [MESH:D013568] <4>(81|94) (88|48|16)
+ + + + 4:   Diseases [MESH:C] <25>
+ + + 3:   Pathologic Processes [MESH:D010335] <65>(45|54) (50|27|12)
+ + + 3:   Skin and Connective Tissue Diseases [MESH:D017437] <2>(38|43) (41|28|20)
+ + 2:   Connective Tissue Diseases [MESH:D003240] <36>(7|10) (10|5|8)
+ + 2:   Fibrosis [MESH:D005355] <12>(4|6) (6|3|3)
+ 1:   Collagen Diseases [MESH:D003095] <10>(2|3) (2|1|0)
+ 1:   Cicatrix [MESH:D002921] <3>(0|1) (0|0|0)
0:   Keloid [MESH:D007627] <2>(0|1) (0|0|0)
- 1:   Acne Keloid [MESH:D000153](0|0) (0|0|0)
- 1:   Torticollis keloids cryptorchidism renal dysplasia [MESH:C536970](0|0) (0|0|0)